Daily Archives: July 23, 2012

GEORGIA TO EXECUTE MENTALLY HANDICAPPED MAN! The Raw Story

 

Thank You for reporting this article now!

“It is a violation of the (constitutional) protections on the death penalty to impose the supreme punishment on individuals suffering from psycho-social handicaps,” said Christof Heyns, of the UN Office of the High Commissioner for Human Rights

By Agence France-Presse
Monday, July 23, 2012 7:24 EDT

Warren Hill Georgia inmate
Topics: supreme court ♦ us supreme court ♦ Warren Hill

Barring a last minute intervention by the US Supreme Court, a mentally handicapped man will be executed Monday in Georgia, despite protests from around the world — and from the victim’s family.

Warren Hill, a 52-year-old African American, has spent the last 21 years on death row for killing a fellow inmate. He was originally put in prison for murdering his girlfriend, according to state authorities.

He is scheduled to be executed Monday, despite his reported IQ of 70, which puts him below the threshold for mental disability.

The US Supreme Court should stop the state of Georgia from executing a man who evidence indicates has significant intellectual disabilities,” Human Rights Watch has said.

But the Georgia Board of Pardons has refused Hill clemency and last Thursday, a Georgia judge ruled that he was intellectually disabled to a lesser degree than the state requires to preclude the death penalty.

The US Supreme Court ruled against the execution of prisoners with mental disabilities in 2002, but left each state with the authority to determine what constitutes mental disability. Georgia maintains mental retardation must be proved “beyond a reasonable doubt.”

In 2003, the Georgia Supreme Court determined Hill’s defense failed to prove mental retardation, and an appeals court upheld the ruling, “even if we believe it incorrect or unwise.”

The US Supreme Court declined to review Hill’s case, but his lawyers have requested that the matter be reconsidered.

“Requiring proof of intellectual disability beyond a reasonable doubt in death penalty cases makes Georgia an extreme and cruel outlier,” said Antonio Ginatta, US advocacy director at Human Rights Watch.

“The Supreme Court should not let Georgia flout the ban on executing people with intellectual disabilities through a legal technicality,” he added.

In a recent editorial, The New York Times said Georgia is the “only state with a statute requiring a defendant to meet the unfairly heavy burden of proving retardation beyond a reasonable doubt. This stringent standard could be readily manipulated by experts, resulting in unconstitutional executions.”

If the execution does occur, Hill will also be the first person in Georgia to be put to death using a single drug, pentobarbital, instead of the standard three-drug cocktail.

A number of organizations have called for Georgia to commute Hill’s sentence to life in prison and high profile figures — including former US president Jimmy Carter, as well as the family of Hill’s victim — have also intervened.

France expressed its “concern about the situation,” asking if the execution could be avoided, while reiterating its call for a universal moratorium on the death penalty.

In a similar case, Yokamon Hearn, 34, was executed in Texas last Wednesday, despite proof he suffered from a mental disorder since childhood.

A UN expert had urged Texas and Georgia to suspend both executions.

“It is a violation of the (constitutional) protections on the death penalty to impose the supreme punishment on individuals suffering from psycho-social handicaps,” said Christof Heyns, of the UN Office of the High Commissioner for Human Rights.

PLEASE LET ME TELL YOU: I AM PERSONALLY GLAD AS A PSYCHOANALYST & BELIEVER: LET’S THANK GOD FOR THIS CHANGE NOW FOR WARREN HILL!

Special thanks to my twitting friends who sent this story,I really hope that publishing it on here will help

 


Vaccines' Genocide

 

Are Vaccines Causing More Disease Than They are Curing?

By Alan Cantwell Jr., M.D.

Vaccines help keep us safe from infectious diseases. Smallpox and polio epidemics have been wiped out by mass vaccine programs. People rush to get flu shots every autumn, and kids are bombarded with a barrage of 22 required vaccinations before the age of six. Even pets need their shots. The manufacture of vaccines is a giant industry and what you pay for – inoculations and doctor visits – is big business for pediatricians, family practitioners and veterinarians. So why are more and more people worried about vaccines, especially the ones for kids?

Vaccine-induced Illness

Barbara Loe Fisher, president of the National Vaccine Information Centre, a consumer’s group based in Virginia, USA, claims vaccines are responsible for the increasing numbers of children and adults who suffer from immune system and neurologic disorders, hyperactivity, learning disabilities, asthma, chronic fatigue syndrome, lupus, rheumatoid arthritis, multiple sclerosis, and seizure disorders. She calls for studies to monitor the long-term effects of mass vaccination and Fisher wants physicians to be absolutely sure these vaccines are safe and not harming people.

No one can deny the dangers of vaccines. The measles, mumps, rubella (German measles) and polio vaccines, all contain live but weakened viruses. Although health officials tell you that polio has been wiped out in the US since 1979, they often fail to mention that all recorded cases of polio since that time are actually caused by the polio vaccine.

Vaccine investigator Neil Z. Miller questions whether we still need the polio vaccine when it causes every new case of polio in the USA. Before mass vaccinations programs began fifty years ago, Miller insists we didn’t have cancer in epidemic numbers, that autoimmune ailments were barely known, and childhood autism did not exist.

Vaccine Contamination

There is also the problem of contamination that has always plagued vaccine makers. During World War II a yellow fever vaccine manufactured with human blood serum was unknowingly contaminated with hepatitis virus and given to the military. As a result, more than 50,000 cases of serum hepatitis broke out among American troops injected with the vaccine.

In the 1960s it was discovered that polio vaccines manufactured in monkey kidney tissue between 1955 and 1963 were contaminated with a monkey virus (Simian Virus, number 40). Although this virus causes cancer in experimental animals, health authorities insist it does not cause problems in humans. But evidence of SV40 genetic material has been popping up in human cancers and normal tissue. Researchers are now connecting SV40-contaminated polio vaccines to an increasing number of rare cancers of the lung (mesothelioma) and bone marrow (multiple myeloma). In a 1999 report, SV40 DNA was detected in tissue samples from four children born after 1982. Three were kidney transplant patients, and a fourth had a kidney tumour. Could SV40 be passed on from parents to their children? No one knows for sure.

Covert Vaccine Experiments

Using kids as guinea pigs in potentially harmful vaccine experiments is every parents’ worst nightmare. This actually happened in 1989-1991 when Kaiser Permanente of Southern California and the US Centres for Disease Control (CDC) jointly conducted a measles vaccine experiment. Without proper parental disclosure, the Yugoslavian-made “high titre” Edmonston-Zagreb measles vaccine was tested on 1,500 poor, primarily black and Latino, inner city children in Los Angeles. Highly recommended by the World Health Organisation (WHO), the high-potency experimental vaccine was previously injected into infants in Mexico, Haiti, and Africa. It was discontinued in these countries when it was discovered that the children were dying in large numbers.

Unbelievably, the measles vaccine caused long-term suppression of the children’s immune system for six months up to three years. As a result, the immunodepressed children died from other diseases in greater numbers than children who had never received the vaccine. Tragically, African girl babies in the experiment were given twice the dose of boys, and therefore suffered a higher death rate. The WHO pulled the vaccine off the market in 1992.

Ironically, the E-Z measles vaccine tested by Kaiser on minority babies was supposed to increase immunity in younger infants. Instead, the vaccine produced the opposite effect. A Los Angeles Times editorial (June 20, 1996) assured readers that “none of the 1,500 was injured by the unlicensed vaccine” and called upon the CDC to ensure that experiments like the E-Z measles vaccine could never occur again.

One wonders how many secret vaccine experiments are conducted by health authorities that never come to the attention of the public. During the two-year measles experiment I was employed by Kaiser and I never knew anything about it until I read the report in The Times five years later, in 1996.

In the poor inner cities across the United States the number of asthma cases is exploding and health officials don’t know why. According to the CDC, 5000 asthma deaths occur annually; and it is estimated that 17.3 million people (4.8 million are children) suffer from the disease, up from 6.7 million in 1980. Asthma usually begins before age 6, and blacks are two to three times more likely to die from asthma than whites. In the Bronx and Harlem sections of New York City, the hospitalisation rate for asthma is 21 times higher than in the more affluent areas of the city.

Could the sharp rise in asthma in poor children be connected with immunosuppression caused by a barrage of vaccines, as well as a lack of quality medical care and insurance, poor diet, and environmental factors? The possible connection of immunosuppressive vaccines to diseases like asthma has never been raised by health officials.

With vaccine experiments frequently performed in Africa and now on black Americans, no wonder one out of every four African-Americans believes AIDS was developed as a genocide program by the US government to exterminate the black population.

But vaccine experiments in the 1990s have not been limited to blacks. Millions of female Mexicans, Nicaraguans and Filipinos have been duped into taking tetanus vaccines, some of which contained a female hormone that could cause miscarriage and sterilisation. In 1995, a Catholic human rights organisation called Human Life International accused the WHO of promoting a Canadian-made tetanus vaccine laced with a pregnancy hormone called human choriogonadotropic hormone (HCG).

Suspicions were aroused when the tetanus vaccine was prescribed in the unusual dose of five multiple injections over a three month period, and recommended only to women of reproductive age. When an unusual number of women experienced vaginal bleeding and miscarriages after the shots, a hormone additive was uncovered as the cause.

Apparently the WHO has been developing and testing anti-fertility vaccines for over two decades. Women receiving the laced tetanus shot not only developed antibodies to tetanus, but they also developed dangerous antibodies to the pregnancy hormone as well. Without this HCG hormone the growth of the fetus is impaired. Consequently, the laced vaccine served as a covert contraceptive device. Commissioned to analyse the vaccine, the Philippines Medical Association found that 20 percent of the WHO tetanus vaccines were contaminated with the hormone. Not surprisingly, the WHO has denied all accusations as “completely false and without basis,” and the major media have never reported on the controversy. For further details on this issue, consult the Human Life International website (www.hli.org).

Newly approved vaccines may also pose serious risks. In October 1999 a vaccine against “rotavirus” infection (which causes most cases of childhood diarrhea) was pulled off the market. One year after the RotaShield vaccine was inoculated into over a million infants, it was found to increase the risk of bowel obstruction. Almost 100 cases of bowel obstruction were reported to the government, and twenty infants developed bowel obstructions within one or two weeks after receiving the vaccine.

Vaccine Manufacture and Associated Dangers

Although the public has heard about side effects of vaccines, most people are clueless about the manufacture of vaccines. Few people know that viruses used in vaccine production need to be grown on animal parts like monkey kidneys, or in chicken embryos, or in human and fetal “cell lines.” Harvesting viruses in human cell-lines can be perilous because some human cell lines are derived from cancer cells.

In AIDS & The Doctors of Death I wrote about the development of the first human “HeLa” cell line – an “immortal” cell line used extensively in cancer and vaccine research for decades. Henrietta Lacks was a young black woman from Baltimore who died from a highly malignant cervical cancer in 1951. Small pieces of her tumour were donated to a laboratory specialising in tissue cell culture. In those days most attempts to grow human cells outside the body failed. But for some unknown reason Henrietta’s cancer cells grew vigorously and became known as the first successful human tissue cell line in history – the now famous HeLa cell line commemorating the legendary HEnrietta LAcks.

Henrietta’s cells were kept alive by feeding them a witches’ brew of beef embryo extract (the ground-up remains of a three-week-old, unborn cattle embryo); fresh chicken plasma obtained from the blood of a live chicken heart; and blood from human placentas (the placenta is the sac that nurtures the developing fetus and contains powerful hormones).

It is now suspected that a sexually-transmitted papilloma virus is the cause of cervical cancer. And it is anybody’s guess how many other chicken, cattle, and human viruses are incorporated into the HeLa cell line, but none of this possible viral contamination seems to bother scientists who have extensively used the cells in cancer research. What laboratory scientists did eventually discover was that HeLa cells proved so hardy that they frequently contaminated other tissue cell lines used in cancer and cancer virus research.

In the late 1960s when widespread HeLa cell contamination problems were uncovered, scientists were shocked and embarrassed to learn that millions of dollars worth of published cancer experiments were ruined. “Liver cells” and “monkey cells” that were used in cancer experiments turned out to be Henrietta’s cancer cells in disguise. Benign cells that supposedly “spontaneously transformed” into malignant cells were found to be cells contaminated with cancerous HeLa cells.

The serious problem of HeLa cell contamination in cancer and vaccine research is revealed in Michael Gold’s A Conspiracy of Cells: One Woman’s Immortal Legacy and the Medical Scandal It Caused. Even Jonas Salk, who developed the legendary Salk polio vaccine, was fooled when HeLa cells contaminated his animal cell lines. He admitted this years later in 1978 before a stunned audience of cell biologists and vaccine makers. In experiments performed in the late 1950s on dying cancer patients, Salk tried injecting them with a cell line of monkey heart tissue – the same cell line he used to harvest polio virus for his famous vaccine. He hoped the monkey cell injections would stimulate the immune system to fight cancer. However, when abscesses developed at the site of injections, Salk began to suspect that he might be injecting HeLa cells rather than monkey cells, and he stopped the experiment.

Mark Nelson-Rees, a HeLa cell expert and one of the 1978 conference attendees, offered to test Salk’s line if it was still available. Salk graciously agreed and the monkey cells indeed proved to be HeLa cells which had invaded and taken over the monkey cell line. According to author Gold, Salk thought there were adequate ways to separate viruses from the tissue cell lines they were harvested in, so that it really didn’t matter what kind of cells were used. Even if vaccines weren’t filtered, and even if whole cancer cells were injected directly into a human, Salk believed they would be rejected by the body and cause no harm. In those days doctors didn’t much believe in cancer-causing viruses. Nowadays, no researcher would dare try injecting cancer cells into a human being. But in the 1950s Salk had done it accidentally. He had injected HeLa cells into a few dozen patients and it hadn’t bothered him a bit.

Is There a Vaccine Contamination
Connection to AIDS?

Most people assume vaccines are “sterile” and germ free. But sterilising a vaccine can destroy the necessary immunising protein that makes it work. Thus, contaminating viruses or viral “particles” can sometime survive the vaccine process.

Animal viruses are also contained in fetal calf serum, a blood product commonly used as a laboratory nutrient to feed various tissue cell cultures. Vaccine contamination by fetal calf serum and its possible relationship to HIV was the subject of a letter by J. Grote, published in the Journal of the Royal (London) Society of Medicine in October 1988. Bovine visna virus (which looks similar to HIV) is a known contaminant of fetal calf serum used in vaccine production and virus-like particles have been detected in vaccines certified for clinical use. Grote warns that “It seems absolutely vital that all vaccines are screened for HIV prior to use, and that bovine visna virus is further investigated as to its relationship to HIV and its possible role in progression towards AIDS.”

Could virus-contaminated vaccines lie at the root of AIDS? A few researchers, including myself, believe HIV was “introduced” into gays during the experimental hepatitis B vaccine trials when thousands of homosexuals were injected in Los Angeles, San Francisco, and New York, during the years 1978-1981.

The AIDS epidemic first erupted in gays living in those cities in 1981. In 1980, one year before, already 20% of the gays inoculated in Manhattan with the experimental vaccine were already HIV-positive. This was several years before definite AIDS cases were diagnosed in Africa. In the early 1970s the hepatitis B vaccine was developed in chimpanzees, now wildly accepted as the animal from which HIV supposedly evolved.

Hepatitis B vaccine was developed to protect people from the sexual spread of the hepatitis B virus. Now the government recommends that all newborn babies be given the vaccine [this is also the case in Australia]. Such recommendations do not make sense to many parents. And people are still fearful of the hepatitis B vaccine because of its original connection to gay men and AIDS. The original experimental vaccine was made from the pooled blood serum of hepatitis-infected homosexuals and, as mentioned, serum-based vaccines cannot be sterilised.

Another theory of AIDS is that HIV originated from polio vaccines contaminated with chimp and monkey viruses, and administered to Africans in the late 1950s. In The River: A Journey to the Source of HIV and AIDS, published in 1999, Edward Hooper details how polio vaccine was made using monkey (and possibly chimp) kidneys and how the ancestor virus of HIV could have jumped species (via the vaccine) to produce the outbreak of AIDS in Africa. Hooper’s well-researched book greatly expands the polio vaccine theory of AIDS first reported by Tom Curtis in Rolling Stone magazine in 1992, and The River is a must-read for anyone interested in the possible man-made origin of AIDS.

Other researchers think it more likely that the various WHO-sponsored vaccine programs (particularly the smallpox program) in Africa in the 1970s are responsible for unleashing AIDS in Africa in the 1980s. Hooper, who has worked as a United Nations official, has discounted the research pointing to AIDS as a man-made disease, as proposed by Dr. Leonard Horowitz in Emerging Viruses, and in my two books AIDS & The Doctors of Death: An Inquiry into the Origin of the AIDS Epidemic and Queer Blood: The Secret AIDS Genocide Plot.

Horowitz and I both suspect contaminated smallpox vaccines as the source of HIV in Africa. Certainly the smallpox (vaccinia-cowpox) virus is an excellent virus to use for the genetic engineering of new, multipurpose vaccines. By splicing into the DNA genes of the vaccinia virus, scientists can add on parts of disease-producing viruses like influenza, hepatitis, and other viruses. The safety of this technique has not been fully evaluated, prompting one vaccine maker at a Vaccinia Virus Workshop in 1984 to ask if this could lead to another form of AIDS.

Vaccine Connection to Gulf War Illness and Huntsville Mystery Illness

The cause of Gulf War Illness (GWI) is unknown. For years this debilitating illness (which now affects one-half of the Gulf War vets) has been ignored by Pentagon officials who claim the disease does not exist and that vets are simply reacting to stress. GWI is also thought to be contagious. Vets insist their disease has been passed on to spouses, other family members, and even pets.

Some people suspect multiple vaccines, particularly the experimental anthrax vaccine, are implicated in the disease. Currently, soldiers who refuse to take the mandatory anthrax vaccine are being court-martialled and dismissed from the service.

Researchers Dr. Garth Nicolson and his wife Nancy have found a tiny bacterial microbe (a “mycoplasma”) in the blood of nearly half the ill vets with GWI. Amazingly, this infectious agent has a piece of HIV (the AIDS virus) attached to it. This microbe could never have occurred naturally. On the contrary, the composition of the microbe suggests a man-made and genetically-engineered biological warfare agent.

Garth Nicolson’s scientific credentials are impeccable. For 16 years he was a professor of medicine at the University of Texas M.D. Anderson Cancer Centre in Houston, as well as professor of pathology and laboratory medicine at the University of Texas Medical School, also in Houston. Nancy Nicolson, a molecular biophysicist, was on the faculty at Baylor College of Medicine.

Six months after returning home from the Gulf War, the Nicolson’s daughter contracted GWI. Her mother Nancy had contracted a similar illness in 1987 when she was working with Mycoplasma incognitus in infectious disease research. Finally suspecting that this research had biowarfare implications, Nancy Nicolson became a whistle-blower and angered officials. As a result, she believes she was deliberately infected with the mycoplasma. After partial paralysis and a long illness, she finally regained her health with the antibiotic Doxycycline.

The Nicolson’s discovery of a similar mycoplasma (but without the attachment of HIV) in a mysterious illness that erupted in the Huntsville, Texas area among prison guards and their families has all the drama of a ‘Movie of the Week’. Although the Huntsville disease broke out in the late 1980s (shortly before the Gulf War), it has many of the same signs and symptoms of GWI. Many locals are convinced the sometimes deadly disease originally spread from prisoners incarcerated in several large prisons around Huntsville.

In experiments conducted during the 1970s and 80s, the prisoners were inoculated with flu vaccines containing genetically engineered viruses and mycoplasma. It is suspected that vaccines were being covertly developed and deployed as biological warfare weapons. Nobel prize winner James Watson, world famous for his discovery of the molecular structure of DNA and a leading researcher of the still ongoing Human Genome Project, was involved in these prison experiments. The guards are convinced the Huntsville mystery illness is intimately connected to these experiments, jointly conducted by the Medical School and the military. Like GWI, health officials deny the disease exists.

The Nicolsons continue to developed antibiotic treatments, which have helped some vets. But they have paid a heavy price for their controversial research and unprecedented discoveries. Garth Nicolson was forced to resign from M.D. Anderson in 1996. His career and reputation destroyed, the Nicolsons have since moved to California and head The Institute for Molecular Medicine in Huntington Beach.

Dangerous Animal and Human Cell Lines
in Vaccine Manufacture

In an effort to quell concerns about the safety of vaccines, scientists are finally taking another look at the “non-infectious” particles of bird-cancer viruses (avian leukosis virus) in the mumps/measles/rubella vaccines routinely given to kids. Could this be the reason the US Federal Drug Administration held a meeting in September, 1999, to reconsider using human tumour cell lines (like HeLa) rather than monkey kidneys and chicken embryos which are no longer guaranteed 100% safe?

Writing in Science, Gretchen Vogel admits public trust in vaccines is a bit shaky. In Wales anti-vaccine parents are holding “measles parties” to infect their children with the disease rather than vaccinate them. She cites the danger of using immortal cell lines for live vaccine production because cancer genes or other hazardous factors might be transferred to people receiving vaccines. But manufacturers also realise vaccine critics are becoming more wary of vaccines made in animal and bird tissue. And vaccine makers want to use immortal cell lines to grow their viruses because obviously viruses can’t grow on their own.

The big question everyone seems to avoid is: Can vaccines cause cancer? There is certainly evidence connecting contaminated vaccines to AIDS. And HIV is a cancer-causing virus. Robert Gallo, the co-discoverer of HIV in 1984, has clearly stated AIDS is an epidemic of cancer.

Animal and avian viruses can contaminate vaccines and have all been studied as cancer-causing agents. And cancer and vaccine research would be much more difficult without the use of cell lines, some of which are derived from cancer.

Vaccines and Public Paranoia

Is the fear of vaccines justified? It is clear that vaccines can be dangerous. The contamination of vaccines is a reality, and vaccine experiments can be hazardous to one’s health. AIDS, unknown two decades ago, is now an increasing worldwide epidemic with millions of death predicted for the next decade. Could vaccines contaminated with cancer-causing and immunosuppressive viruses unleash new plagues in the New Millennium? If so, the new plagues may be far worse than the diseases we eradicated by vaccine programs in the twentieth century.

References

“Anti-diarrheal vaccine for babies recalled,” Los Angeles Times, October 16, 1999.

Butel JS, Arrington AS, Wong C, et al.: Molecular evidence of simian virus 40 infections in children. J Infect Dis 180:884-887, 1999.

Cantwell A: AIDS & the Doctors of Death. Aries Rising Press, Los Angeles, 1988.

Cantwell A: Queer Blood. Aries Rising Press, Los Angeles, 1993.

Gold M: A Conspiracy of Cells. State University of New York Press, Albany, 1986.

Hooper E: The River: A Journey to the Source of HIV and AIDS. Little, Brown and Company, Boston, 1999.

Horowitz L: Emerging Viruses: AIDS & Ebola. Tetrahedron, Inc, Rockport, MA, 1996.

Jaroff Leon: “Vaccine Jitters,” TIME, September 13, 1999.

Likoudis P: “Gulf war illness probe to advance with new study,” The Wanderer, January 21, 1999.

“Measles, government and trust ” (Editorial), Los Angeles Times, June 20, 1996.

Miller NZ: Immunization: Theory vs Reality. New Atlantean Press, Santa Fe, 1996.

Miller NZ: Immunizations: The People Speak! New Atlantean Press, Santa Fe, 1996.

Quinnan GV: Vaccinia Viruses as Vectors for Vaccine Antigens. Elsevier, New York, 1985.

Stolberg SG: “Poor fight baffling surge in asthma,” New York Times, October 18, 1999.
Source

 


Anthrax in South Africa: Economics, Experiment and the Mass Vaccination of Animals, 1910–1945

 

During 1923, the South African government began to issue free vaccine for the immunization of cattle against anthrax. Five years later, it introduced compulsory annual vaccination in parts of the Transkeian Territories, an area reserved for occupation by Africans. Thereafter, the state sought to extend both compulsory and discretionary vaccination. In 1942, scientists at the government’s Onderstepoort Veterinary Institute announced that they had issued 6 million doses of vaccine during the previous year. Approximately half the cattle in the country were being immunized annually with a special product which scientists at the Institute had recently devised.1 The scale of vaccination was unprecedented within the country and the annual issue of anthrax vaccine far surpassed the amount supplied for any other animal disease. It was a major state intervention in rural society. Nevertheless, vaccination against anthrax in South Africa is absent from the historiography, while published contemporary accounts are few.2

The history of anthrax control in South Africa, which concerns public policy and technical innovation, relates to the wider historiography of medicine, science and technology in the British Empire. If Daniel Headrick has interpreted various innovations in science and medicine as “tools of empire”, which enabled colonists to conquer indigenous populations and overcome hostile environmental conditions,3 historians have more recently been concerned with the ways in which western medicine assisted colonial administrations in extending social control over the colonized.4 Medical science underpinned militaristic public health policies and sanitary measures, in which vaccination, particularly against smallpox, at times played a significant part.5 In Africa, such interventions sometimes disrupted long-established methods of disease control based on environmental regulation, with disastrous results for the health of the colonized.6

In South Africa too, historians have been concerned with the relation of racially biased medical institutions, public policies and private practice to the imposition and development of segregation and apartheid.7 In this regard, however, Harriet Deacon has suggested a contradiction between the analysis of western medicine as a means by which the state extended control over Africans and the argument that Africans have suffered because they have been excluded from the benefits to health that it has potentially offered.8

A similar contradiction is evident in the rather scant historiography of state veterinary services and science in South Africa (and elsewhere in the continent).9 While more detailed accounts of veterinary scientists and their activities have begun to emerge,10 veterinary science has been interpreted generally as a means of enabling white “settler” stock farmers to overcome problems of production posed by disease and environment, or even as an indirect subsidy to enable them to overcome competition from African producers.11 Historians have also focused on political conflict associated with state interventions aimed at controlling rinderpest and East Coast fever among African-owned cattle, arguing that these epizootics were occasions on which the state sought to extend political and social control over Africans.12 The extension of veterinary services to African-owned stock through vaccination against anthrax is, however, incongruent with these interpretations of state policy. While it may be argued that state attempts to control anthrax in African areas were intended to benefit white stock farming by tackling possible sources of infection, the idea that state veterinary services operated simply for its benefit needs to be qualified. The motivation for the extension of state veterinary services to African areas, and the way it functioned in practice, requires further analysis. I argue that mass vaccination in African areas, made possible by the operation of bureaucratic regulatory systems and asymmetrical power relations in a racially segregated society, was an important means by which state-employed veterinary scientists acquired knowledge about the disease and evaluated innovations in vaccine technology.

During the 1920s, officials in the Department of Agriculture became increasingly concerned about the threat of restrictions upon pastoral exports from South Africa because of their contamination with anthrax. In response, government vets promoted and later enforced vaccination against the disease, but for various reasons the practice was unsatisfactory as a method of prevention and control. This led to a period of experiment during which South African veterinary scientists sought to develop improved vaccines through technological innovation. The compulsory vaccination of African-owned cattle provided a means of obtaining a statistical basis for the evaluation of these new methods and products.13 Laboratory investigations and field vaccination, with associated state-enforced regulations, were thus components of an experimental system in which the results obtained by vets in the field informed both technological adjustment and social policy.14 Vaccination against anthrax in African-occupied areas such as the Transkei, carried out under the control of state officials, was a means of testing a technology which was eventually used throughout South Africa and more widely around the world. I examine experimental method in the investigation of anthrax and the development of the vaccine in some detail. This article is therefore intended to contribute to the historiography of scientific practice in bacteriology and immunology during the 1920s and 1930s.15

The first part provides context by describing the establishment and growth of state veterinary institutions and services as a response to problems of disease. In the second part, I describe how officials became increasingly concerned with the prevention and control of anthrax during the early 1920s, particularly in the context of international attempts to protect workers in the textile industry from the danger of contaminated wool and hair. In the third part, I examine veterinary ideas about the nature of anthrax in South Africa and attempts at control up to the 1930s, showing how the compulsory mass vaccination of African-owned cattle became an important component of state policy. Government veterinary scientists, however, emphasized various perceived peculiarities of anthrax in the region and argued that these limited the value of imported technological systems during a period when the practice of vaccination greatly expanded. The final section analyses laboratory experiments and technical innovations, the use of statistical studies obtained through compulsory mass vaccination and the further extension of the practice.
Go to:
The Animal Economy and Veterinary Institutions

Domestic animals provided an important source of food and traction for the indigenous peoples of southern Africa and the early Dutch colonists at the Cape. From the 1820s, when the British government actively encouraged immigration to the Cape of Good Hope, pastoral production became increasingly commercialized. The new colonists imported wool-producing merino sheep, which thrived in the semi-arid Karoo and in parts of the Eastern Cape. As production increased rapidly through the mid-nineteenth century, wool became the Cape’s major export, its sale on the British markets drawing the colony into the international economy. Later, wool exports were substantially supplemented by the production of mohair from angora goats, another settler import. While the expansion of diamond mining from the 1870s, and gold mining from the 1890s, transformed southern African societies, the exploitation of minerals did not displace pastoralism as a pillar of South Africa’s economy until after the mid-twentieth century.16 Furthermore, the urbanization which followed the large-scale exploitation of minerals created markets for meat and dairy products, further stimulating the growth of commercial pastoralism. During the late nineteenth century, parts of the Eastern Cape became important centres for cattle farming and dairying, while colonial pastoralists sought to develop ranch-style beef production on the grasslands of the Northern Cape and, from the early twentieth century, in the adjoining parts of the Western Transvaal.17 White commercial pastoral farming was therefore a major concern of the South African government throughout the period under review.

The expansion of commercial pastoralism, however, was neither continuous nor without problems. From the 1870s, colonist farmers, particularly in the wetter, eastern parts of the Cape and in Natal, became increasingly convinced that stock diseases presented serious obstacles to the expansion of animal numbers. The population of sheep and angora goats in some of the Eastern Cape districts began to decline very rapidly during the 1870s and the concerns of farmers resulted in the appointment of the first government veterinary surgeon in the Cape during 1876, following a similar appointment in Natal. Farmers who gave evidence to the Cape’s Stock Diseases Commission of 1877 described how mysterious diseases had destroyed many flocks. The early government vets sought to investigate these diseases, but the small number of appointments, together with a heavy administrative burden, meant that they made little progress in this direction until the end of the nineteenth century.18

The African rinderpest epidemic, which reached southern Africa in 1896 and threatened to devastate cattle holdings, was a major impetus to the expansion of veterinary services. Thereafter, additional professional appointments at the Cape enabled state-employed veterinary scientists to engage in more systematic research.19 Following British victory over the Afrikaner republics of the Transvaal and Orange Free State in the South African War (1899–1901), Lord Alfred Milner supervised the reconstruction of the defeated states, with the objective of a unified South Africa.20 Milner, a prime exponent of constructive imperialism, was committed to harnessing science to the development of “settler” commercial agriculture, a policy which was accompanied by the exclusion of African peasant producers. He set up a modernizing Department of Agriculture, including the Swiss-trained veterinary scientist Arnold Theiler to undertake research.21 A British vet, Stewart Stockman, was appointed to lead a veterinary department consisting largely of British-trained practitioners, the major function of which was the control of infectious and contagious diseases in the field.22

In 1902, the highly virulent tick-borne disease of cattle, East Coast fever, broke out in the Transvaal. Over the next ten years, it spread throughout the Transvaal lowveld, Natal, the Transkei and into the Eastern Cape, where the environmental conditions supported the tick vector. East Coast fever, which produced morbidity and mortality rates above 90 per cent, threatened to destroy the cattle industry of South Africa and made state veterinary services indispensable. It provoked a vigorous, if sometimes politically controversial response from the Transvaal’s new veterinary department, which was based on an extensive regulatory system consisting of the dipping of cattle against ticks, movement embargoes, quarantines and sometimes the destruction of the infected herd. East Coast fever remained a major preoccupation of the veterinary department until it was finally eradicated from South Africa during the 1950s.23

Throughout the 1900s, Arnold Theiler conducted research into various aspects of East Coast fever, which provided the knowledge base for control measures. He was rewarded, in 1908, with modern laboratory facilities at Onderstepoort, about ten miles north of Pretoria. Following the establishment of the Union of South Africa in 1910, the Onderstepoort Veterinary Bacteriological Laboratories, later the Onderstepoort Veterinary Institute, became the centre for veterinary research throughout South Africa. Theiler oversaw the inauguration of a veterinary faculty as part of the University of Pretoria in 1920, which awarded degrees and doctorates in veterinary medicine. Thus began a period during which the veterinary profession was increasingly “South Africanized” and the pursuit of research became less dependent on imported expertise. By the 1930s, veterinary appointees were typically white, male South Africans, frequently the sons of farmers. Theiler retired in 1927 and a new director, Petrus Johann du Toit, an Afrikaner, was appointed as his replacement. Du Toit’s appointment was accompanied by a significant bureaucratic reorganization, as the veterinary field services were now formally brought under Onderstepoort’s control. Du Toit thus took charge of the overall formulation of veterinary policy and field activities, as well as research.24

As East Coast fever was gradually controlled during the 1910s, the research agenda at Onderstepoort diversified. Given the increasingly segregationist nature of South African society, the overall direction of research was determined largely by the concerns of white farmers. A series of groundbreaking studies in plant toxicology, botulism in animals and nutrition, which were of wider relevance to pastoralism throughout the world than the early work on “tropical animal diseases”, such as East Coast fever, brought the Institute to international prominence during the 1920s. Immunological studies, many of which adapted technological innovations made in metropolitan countries, were an important component of research during the 1930s. Veterinary scientists working at Onderstepoort released vaccines against the insect-borne viral diseases African horsesickness and bluetongue (sheep) and against anthrax. These vaccines and associated technologies were exported to other parts of the British Empire and beyond, further bolstering the reputation of the Institute abroad and enabling it to take an increasingly prominent part in the “polycentric communications network” of international veterinary science.25
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Anthrax and the Origins of an Economic Problem

The origins of anthrax in South Africa are obscure, but by at least the mid-nineteenth century the disease was familiar to Anglophone farmers and Dutch pastoralists, who called it “miltziekte” (spleen sickness) because of the swollen spleen which they found on post-mortem examination. The British vets employed as government officials in the Cape Colony and Natal during the 1870s were also familiar with this fatal disease. The first government vet at the Cape, William Catton Branford, saw cases of anthrax shortly after his appointment in 1876. He advised farmers not to dismember the carcasses, but to bury them intact with quicklime to prevent the contamination of the pasture with the anthrax organism.26

During the 1890s, the Cape government vets perceived anthrax as an increasingly serious and widespread hazard. Otto Henning, a state-employed vet who worked in the commercial cattle-ranching areas of the Northern Cape and British Bechuanaland (annexed to the Cape in 1895), thought the disease was gaining a significant hold and that some farms had become badly contaminated. Following the British victory in the South African War in 1901, newly-appointed veterinary officials found that contiguous parts of the Western Transvaal, an area which Milner’s reconstruction government had prioritized for the development of settler cattle farming, had acquired an “evil reputation” for anthrax among local farmers.27 The vets also became increasingly concerned about the prevalence of the disease along the roads between the ports of the Eastern Cape and the Transkei. Both white and African transport riders, the vets claimed, frequently left anthrax carcasses unburied were they had fallen, causing long-term contamination. Some “outspans” on the transport riding routes were allegedly hotbeds of infection.28

During the 1910s, government vets became convinced that the large majority of anthrax cases went unreported and that the disease was far more common than the official statistics suggested.29 In this regard, the intensified veterinary supervision that followed the imposition of the East Coast fever regulations (which required the submission of blood smears for every cattle death in proclaimed areas) in the Transkei during 1910 enabled officials to gain a clearer insight. The number of cases detected rose dramatically after the imposition of the regulations,30 and a similar increase followed the proclamation of the Eastern Cape districts of Kingwilliamstown and East London shortly afterwards.31 The vets believed that without the regulations most of these outbreaks would have gone undetected, and speculated that closer inspection would reveal a similar picture in other parts of the country.32 Nevertheless, the annual number of reported deaths from anthrax remained quite small. During 1920, for example, 1,891 outbreaks of the disease were reported in South Africa, killing just over 6,000 cattle.33 While the number of deaths was small as a percentage of the overall population of approximately 6 million cattle, the vets emphasized the potential for the disease to contaminate farms and make them unworkable. Throughout the 1910s they accordingly pressed for the enforcement of measures of control.34

The initial motivation for a more thorough policy of control and prevention after 1920, however, lay in the threat anthrax posed to human health abroad.35 In Britain and America there was, during the 1910s, continuing concern about the small but persistent number of cases of anthrax infection among workers handling imported wool and hair. The chief danger was the inhalation of the anthrax organism, which caused the potentially fatal “woolsorters’” disease. During 1916, the United States government promulgated regulations requiring the disinfection of animal products from regions in which anthrax was prevalent.36 The American consul immediately refused to certify hides from the Transvaal, effectively closing the American market to South African producers.37

With regard to Britain, the major export market for South African wool and mohair, the situation was potentially more serious. In 1910, the Anthrax Investigation Board of Bradford detected anthrax in samples of bloodstained South African mohair.38 A Departmental Committee on anthrax (appointed in 1914) recommended the construction of a pilot disinfection plant to treat wool and mohair from countries in which contamination was likely.39 It also evaluated the prevalence of anthrax and measures for its control in the exporting colonies. The Committee found that the situation in Australia and New Zealand was satisfactory, but the lack of efficient controls in Egypt and India meant that their products would require disinfection.40 The position with regard to South Africa was less clear. The Committee found that “the state of civilisation” there was sufficient for anthrax to be “stamped out”, but “the desirability of applying disinfection would have to be considered”.41

Given the importance of wool and other pastoral exports to the South African economy, the perceived threat to trade caused some alarm among the South African government. Officials in the Department of Agriculture calculated that should Britain impose compulsory disinfection, the estimated surcharge of around one and a half pence per pound in weight of wool would entail a cost of over £1,000,000 per annum to producers.42 Furthermore, they were in danger of being excluded from the group of settler colonies and classified with India and Egypt, a prospect that fitted ill with the government’s “progressive” and segregationist ideology. In 1918, a Central Wool Committee, set up under Barney Enslin, the head of the Division of Sheep, was extremely critical of current practices in the wool trade, in which fleeces were stored indiscriminately with blood-stained cattle hides, believed to be the major source of infection.43 The Department of Agriculture, anxious to publicize the anthrax problem, issued a press circular emphasizing the threat to producers.44 At the same time the Chief Veterinary Surgeon, Charles Gray, warned that, “Unless stock owners bestir themselves and take this disease more seriously, it is more than likely that other countries will place an embargo upon the introduction of animal products from South Africa, which will react detrimentally upon the prosperity of the farmer”.45

At the Colonial Office, Lord Milner, who had supervised the construction of a unified South African state, was apparently anxious that the colony’s products should continue to be exempt from disinfection. He sought assurances from the Governor-General that South Africa was doing everything in its power to ensure the prevention and eradication of anthrax.46 When the disinfection plant, which was situated in Liverpool, came into operation in July 1921, Egyptian and Indian wool and goat hair were subject to compulsory disinfection, while South African products remained for the time being exempt.47 Nevertheless, the problem of the contamination of South African products remained. In November 1922, the Colonial Office warned the Governor-General that investigators had detected the anthrax organism in Cape mohair on eleven occasions between September 1921 and August 1922.48

After the First World War, efforts to protect textile workers against infection became internationalized. The International Labour Office set up an Anthrax Commission to investigate the disease around the world. In 1922, the Commission, which was attended by the Cape’s Senior Veterinary Officer, Rowland Dixon,49 reported that the Liverpool disinfection plant had been successful in reducing the incidence of infection and recommended the establishment of other plants in producing countries where anthrax was prevalent. South African mohair was mentioned specifically as a likely source of infection.50 Dixon returned to South Africa urging the need to instigate more effective measures of control. In fact, the threat of compulsory disinfection declined from the mid-1920s, as the British Treasury resisted further expenditure on the Liverpool plant and the International Labour Commission failed to pass a convention requiring universal disinfection of wool and hair, instead concentrating on the threat posed by contaminated cattle hides.51 Nevertheless, in 1928 Petrus du Toit, as the newly appointed head of South Africa’s veterinary services, warned of the continued vigilance of the health section of the League of Nations. Compulsory disinfection would, he reiterated, impose a substantial cost on South African producers.52 If the threat of embargoes faded by the 1930s, however, officials in South Africa continued to stress the potential of the disease to contaminate pastures, and anthrax remained a major veterinary preoccupation.
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The Veterinary Conception of “South African Anthrax” and Control to the 1930s

The framing of regulations aimed at the control of anthrax in the late nineteenth and early twentieth centuries depended on contemporary understandings of the causal organism, Bacillus anthracis, which had been extensively investigated by Robert Koch during the late 1870s.53 As an infected animal approached death, its blood swarmed with millions of the bacilli in the vegetative (multiplicative) form. Once it died, the conditions necessary for the multiplication of the bacilli failed. At moderate temperatures and in the presence of free oxygen, they transformed into inert, highly resistant spores. As the carcass disintegrated, the spores, which could remain viable for an indeterminate period, were deposited on the pasture. If spores entered the blood-stream of a grazing animal through abrasions in the mouth or alimentary tract, they returned to the vegetative state, setting up fatal disease and repeating the cycle of infection and contamination. Anthrax, however, was not considered a contagious disease which passed directly from an infected to a healthy animal.54

The South African Stock Diseases Act of 1911, which consolidated existing legislation in the various colonies relating to anthrax (and other contagious and infectious animal diseases), was drafted to deal with the ability of Bacillus anthracis to contaminate through sporulation.55 The regulations required owners to report all suspicious deaths to the police or veterinary officials and to submit a blood smear, taken from a small cut in the ear, for laboratory examination. They expressly forbade the opening or dismemberment of the carcass for meat, as this would lead to sporulation and the contamination of the pasture. Owners were required to cremate the carcass promptly or to bury it deeply with quicklime. If the smear tested positive, owners were required to fence off the immediate area to prevent the infection of other animals. As the incubation period of anthrax was short, vets enforced only a brief quarantine to detect associated cases.56

These aspects of the South African regulations were based largely upon the British model, which insisted on the control of anthrax by hygienic measures without recourse to Pasteurian vaccination.57 Since the rinderpest (cattle plague) epizootic of the mid-1860s, when this disease had been eradicated through the rigorous application of quarantine, slaughter and import embargoes, British veterinary policy had followed a particular trajectory. Based on what Michael Worboys has called “importation theory”,58 it aimed at the eradication of contagious and infectious diseases through slaughter and the prevention of reinfection through import embargoes. With regard to anthrax, this policy was the outcome of several factors which made eradication through hygienic measures an achievable aim. Anthrax was a relatively rare disease in Britain and the state had sufficient resources to detect cases. Furthermore, given the insular nature of the country, it was possible to prevent the importation of infected animals. Thus, the British veterinary authorities relied on hygienic measures and discouraged vaccination, which they believed could occasionally cause infection.59

By the early twentieth century, however, British-trained veterinary officials in South Africa were convinced that a policy of relying on hygiene alone would fail to control anthrax, given various local circumstances. In contrast to the British example, vaccination became an important element of public policy from the 1910s. There were several reasons for this, which related to the conditions of cattle production in the region and ideas about the nature of the disease itself. The vets considered that the strict enforcement of the regulations under the local conditions of predominantly extensive pastoralism in both white and African areas was impossible. The power of the state to detect outbreaks was limited by the relative weakness of its administration and policing on the ground. Vets working in the field knew from experience that many stockowners did not report cases if they thought these were likely to go undetected by officials. In this regard, the veterinary discussion of the nature of the anthrax problem assumed a distinctly racist tone. According to one government vet, Andrew Goodall, African stockowners were “in the front rank of all our transmitting agents”,60 while the senior vet, Philip Viljoen argued that, “There is unfortunately a further complication, namely, the native who, generally speaking, is careless in his farming methods and, above all, does not understand food hygiene”.61

Veterinary officials thought that there were three centres of particularly dense anthrax contamination: the Northern Cape districts, such as Vryburg, which had formerly been part of British Bechuanaland and which had been annexed to the Cape in 1895, the Transkei and the Witwatersrand.62 In all three areas, they associated anthrax infection with African-owned cattle and linked its persistence and spread to African practices. The key problem, the vets argued, was that in cases of anthrax Africans flouted the regulations by removing the saleable hide and cutting up the carcass for meat. The Irish veterinarian Daniel Kehoe, who studied anthrax in South Africa during the 1910s, reported that the disease was common along the Witwatersrand, a relatively urbanized area in which gold mining was the principal economic activity. As urbanization based on mining progressed, the increasing number of Africans living in compounds and locations along the Rand provided a growing market for milk and meat. Kehoe reported that there were many milch cows on unfenced plots around the African townships. When an animal died, he alleged, the owner typically evaded the municipal sanitary charge for disposal of the carcass by allowing “mine natives” to cut it up for meat. This, argued the vets, was an efficient means of disseminating anthrax infection across a comparatively densely populated area.63 These hides were a prime means of contaminating wool and mohair intended for export, while the practice of dismemberment allowed the sporulation and more widespread distribution of the bacilli.64 The vets, however, did not think that these practices were necessarily rooted in ignorance. Africans were familiar with the disease and seemingly aware of the dangers. According to the botanist, Andrew Smith (writing in the late nineteenth century), Africans rendered infected meat harmless by boiling it with certain herbs, such as Zanthoxylon capensis, then referred to as wild cardamom.65 The vets, however, had apparently little interest in investigating the possible disinfectant properties of these plants, even though they were uncertain whether boiling alone was always an effective means of sterilizing meat.66

Thus, while European farmers were not exonerated, veterinary officials tended to cast the problem of anthrax control as one which related particularly to Africans. In the reserves of the Northern Cape and the Transkei, where African stockowners grazed their herds on communal pastures, places where large numbers of cattle collected regularly, such as watering points, could become badly contaminated with anthrax spores. Veterinary policy makers believed that they lacked the resources to impose comprehensive measures of hygiene in African areas. In the words of one vet, the suppression of anthrax in areas occupied primarily or wholly by Africans “presents tremendous difficulties”, because of extensive communal pastures.67

Furthermore, in South Africa anthrax seemed to display particular characteristics. As in Britain, it appeared to be primarily a disease of cattle rather than sheep (as in France and Australia), although the vets admitted that cases in sheep would be difficult to detect under conditions of extensive farming.68 The contamination of fleeces probably resulted from contact with other materials, such as cattle hides, rather than from infection in the sheep. Thus, the vets thought that contamination of wool and mohair was a function of infection among cattle.69 The vets found a partial explanation for this in the grazing habits of the different species of domestic animals. On the grasslands of Griqualand West in the Northern Cape, where anthrax was common, cattle grazed the grass closely and were liable to pick up spores from the soil. Infection was more likely if prickly pear was present, because the spiny skins could puncture the mouths of grazing animals, thereby providing a means for spores to enter the bloodstream.70 In the Karoo, where the disease was virtually unknown, sheep fed upon the leaves of bushes away from the ground and were therefore less likely to ingest spores. The comparative frequency of infection in cattle was the subject of some speculation. Researchers at Onderstepoort found it difficult to infect cattle even by injecting very large amounts of virulent material, but infection was quite common in nature. It was possible that strains of extreme virulence existed in South Africa, which caused frequent outbreaks in the relatively resistant bovine.71 Thus, the species principally affected was of relatively high unit value, which tended to make vaccination an economically justifiable practice.

Vets in South Africa tended to stress the importance of environmental factors in the transmission and dissemination of anthrax. If British veterinarians regarded Bacillus anthracis as an “obligatory” parasite, propagating only in the living animal, little was known about how the organism behaved in nature. Given the appropriate environmental conditions, the vets speculated, it might be able to multiply outside the body. Watering holes were important locations for the transmission of the bacilli, which were possibly able to proliferate in damp soils, rich with decaying matter.72 Climate too seemed to have some bearing, as outbreaks were more common after the commencement of summer rains.73 While they agreed that the original source of contamination was the carcass of an infected animal, vets noted a tendency for the disease to spread along watercourses and surmised that flowing water carried spores downstream.74 Carrion-eating mammals and birds were highly resistant to anthrax, but they probably disseminated the spores over wide areas by depositing them in their excreta. While outbreaks were usually localized affairs that produced relatively few deaths, anthrax sometimes assumed an epidemic form, particularly among horses. This was especially the case in Griqualand West and the Western Orange Free State, where the horsefly (Hippobosca rufipes) proliferated. Vets believed that this fly could carry Bacillus anthracis rapidly beyond the immediate centre of infection, causing localized epidemics, a theory which had also been advanced in the United States.75 Given these observations, it seemed possible that Bacillus anthracis was not entirely dependent on the infected animal for propagation and transmission. The evidence suggested that slaughter and hygiene would not be an entirely effective method of controlling the disease.

These considerations meant that, as in much of Western Europe, Australia and United States, where anthrax was widely disseminated across extensive grasslands, vaccination was an important component of state veterinary strategy to control anthrax in South Africa. Unlike in Britain, veterinary officials actively encouraged the use of Pasteur’s vaccine to protect in-contact animals in individual outbreaks.76 Vaccine was first imported to the Cape from France in the early 1880s, soon after its initial demonstration, but the amount used remained small until the promulgation of the Stock Diseases Act of 1911, which empowered government vets to enforce the vaccination of in-contacts at the owner’s expense. Voluntary vaccination, however, was also increasingly popular among the stock-owning public, so that the annual issue of anthrax vaccine increased from around 40,000 doses in 1911 to 1,200,000 in 1920.77

Given the perceived threat of the compulsory disinfection of wool exports during the early 1920s, the state, now “prepared to do everything in its power to get the disease under proper control”, instigated a more determined policy of prevention based on the availability of sufficient effective vaccine.78 While veterinary scientists continued to stress the importance of hygienic measures, they increasingly encouraged vaccination, which expanded accordingly.79 Until 1915, Onderstepoort imported vaccine from the Pasteur Institute in Paris, but when the First World War interrupted the supply Theiler instructed Kehoe to initiate local production. During 1922, Theiler pressed for legislation giving Onderstepoort control of the supply of anthrax vaccine. As vaccination was now being carried out on a large scale, he argued, the South African farmer needed protection against unduly expensive and possibly defective imported products, which might introduce other infections. It was equally important to prevent the marketing of potentially dangerous vaccines by local amateurs.80 Regulations promulgated in 1923 empowered Onderstepoort to forbid the importation of any vaccine from abroad and to suppress local manufacture, a policy that was carried out vigorously.81 In effect, Onderstepoort obtained a monopoly of the supply of anthrax vaccine within the country.

If vets could oblige stockowners to vaccinate in-contact animals during any outbreak, by the early 1920s they believed that the cost of the vaccine tended to discourage farmers from reporting.82 To overcome this problem, the government began, from July 1923, to issue free vaccine to stockowners upon request.83 Thereafter the use of the vaccine increased rapidly, so that by 1925 Onderstepoort was issuing approximately 2.5 million doses annually.84 From the point of view of the veterinary field service, the issue of free vaccine considerably aided control by encouraging notification as required by the Act. The policy continued until 1936, by which time the vets believed that farmers were misusing or wasting large amounts and reintroduced a charge.85 Vaccine was still substantially subsidized, however, as the levy of two shillings and sixpence per hundred doses was a quarter of the estimated cost of production. After 1936, the Department of Native Affairs paid for the vaccination of African-owned stock, except in the Transkei, where it was funded out of the existing cattle-dipping tax.86 Policy towards the racial groups, however, was different, as vaccination of African-owned livestock was more tightly controlled, with government vets or stock inspectors performing the operation rather than the owners themselves.87

Furthermore, senior vets argued that, given the inadequacies of detection, the best method of control and prevention was the compulsory annual vaccination of all cattle in areas considered severely or extensively infected.88 During the 1920s and 1930s, however, the state enforced compulsory vaccination in African areas only. This was determined by the vets’ racially biased explanation of the incidence of anthrax and by asymmetric relations of political power between the state, its European constituency and disenfranchized Africans in a segregationist society. Compulsory vaccination was initially enforced across individual African locations during the 1920s at the behest of European farmers in Northern Cape districts such as Barkly West. Here African locations holding large numbers of cattle lay in close proximity to white commercial ranches.89

If local European concerns about disease “reservoirs” lay behind this piecemeal vaccination, a more systematic and overarching policy of “block” vaccination began to emerge in the late 1920s, particularly with regard to the Transkeian Territories. The execution of compulsory “block” vaccination was associated with John Nicol, a British-trained vet appointed, in 1928, Chief Veterinary Officer for the Transkei by Petrus du Toit, who was now in charge of field services. Since joining the Cape Veterinary Department in 1910, Nicol had accrued much experience of working among Africans and their stock in the Eastern Cape and the Transkei, where his major task had been the enforcement of the East Coast fever regulations. In August 1928, after consulting with the resident magistrate (the head administrative officer), Nicol began the inoculation of all the cattle in Engcobo, a district in the western Transkei which usually accounted for a quarter of the total number of cases detected in the Territories.90 Vaccination seems to have been politically uncontroversial and it was rarely mentioned in the discussions of the Transkei’s governing body, the General Council. Comment was favourable, apart from some discussion on how the costs should be allocated.91 Some Transkeian stockowners were already using free vaccine on a voluntary basis and there were the precedents of earlier inoculations against rinderpest and “lungsickness” (contagious bovine pleuropneumonia).92

The anthrax situation in the Transkei came to be of special interest to the vets because they believed that the operation of the East Coast fever regulations gave them a particularly accurate picture of the incidence of the disease there. The regulations, which had been in force in the Transkei since 1910, entailed a strong element of social control, limiting the free movement of cattle and enforcing regular insecticidal dipping.93 In 1929, du Toit and his colleagues at Onderstepoort, now formally directing field services, initiated a policy of “intensive control”, which required stock inspectors to take a regular two-weekly census of cattle in proclaimed areas, while blood smears for diagnostic examination were taken from any cattle that died or were slaughtered. The vets believed that as “intensive control” of East Coast fever would enable them to detect any cases of anthrax that occurred in the Transkei, they would obtain accurate data on the rate and distribution of infection.94

In this regard, the vets perceived compulsory vaccination in Engcobo to be an immediate success. Nicol reported that during the year following the introduction of immunization, the number of outbreaks recorded in Engcobo dropped from 61 to 15. Although the government’s own statistics showed that anthrax was no more common in the Transkei than in some other major cattle holding areas, the vets targeted it for a pilot anthrax vaccination “campaign”. Accordingly, Nicol, in collaboration with the magistrates, extended compulsory vaccination to the rest of the western districts of the Transkei in 1929 and to the whole of the Territories by 1934. The only exception was the settler-dominated district of Mount Currie, where vaccination remained voluntary.95 By 1942, Nicol announced that his staff were overseeing the annual vaccination of over 1,600,000 cattle in the Transkei—virtually complete coverage.96

During the early 1930s, compulsory annual vaccination was extended to other African reserves in various parts of the country. Coverage was less complete than in the Transkei, with “campaigns” targeted at “blocks” of territory thought to be severely affected. Nevertheless, officials conducted these operations on a large scale. In 1933, the Secretaries for Agriculture and Native Affairs, acting on veterinary advice, ordered the annual vaccination of over a quarter of a million head of cattle in five districts in Northern Zululand.97 The policy was extended further in Natal, so that by 1937, compulsory vaccination was in force in 101 different African reserves and in locations throughout Natal and Zululand, entailing the treatment of over a million cattle every year.98 Compulsory vaccination was intensified in the Griqualand West area, where wholesale vaccination was ordered whenever a case of anthrax was reported in a particular reserve.99 Officials initiated similar measures across the Transvaal so that, by the late 1930s, annual compulsory vaccination was in place in fifty-seven African reserves, entailing the treatment of over one-quarter of a million cattle each year.100 During 1940, more than 6 million head of cattle, half the total South African population, were vaccinated.101 South African officials also encouraged vaccination in neighbouring states by offering to export vaccine to Swaziland, Basutoland (Lesotho), South West Africa and Bechuanaland (Botswana) at the price of five shillings per hundred doses, substantially below the estimated cost of production.102
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Experimenting with Anthrax: Max Sterne, the Invention of an “Avirulent” Vaccine and the Experimental Function of Mass Vaccination

If vaccination was in force extensively with an apparent degree of success in South Africa by the 1930s, the practice was not without problems of safety and effectiveness. Difficulties with imported systems of vaccination and associated technology meant that these were subject to critical review by veterinary scientists at Onderstepoort, where an experimental approach to the production and use of vaccine evolved from the mid-1910s through to the 1940s. During the 1930s, the results obtained by mass compulsory vaccination of African-owned cattle came to fulfil an important function in these experiments.

The active constituent of the vaccine first manufactured in South Africa during 1915 was an attenuated strain of the bacillus obtained from the Pasteur Institute in Paris. The key variable determining the safety and efficacy of vaccine was thought to be the degree to which the pathogenic property of the bacilli was reduced through attenuation, achieved by heating according to Pasteur’s method.103 In terms of contemporary theory, the bacilli needed to be attenuated to a point at which they could no longer cause disease, but were still capable of conferring immunity by stimulating the production of antibodies within the body. The question of attenuation was complicated by variability in the susceptibility of different species of domestic animals. Vets believed, for example, that horses and angora goats were more susceptible than cattle and sheep, so their safe immunization required a more attenuated vaccine. In practice, Pasteurian vaccination consisted of two injections, carried out approximately fourteen days apart. The first used highly attenuated organisms to stimulate an initial immune response, while the second contained less attenuated organisms, which produced immunity sufficient to prevent natural infection. Scientists considered that this protection lasted for little more that a year, so they recommended annual vaccination as a means of maintaining continuous immunity.104

Both vets and farmers criticized the Pasteur vaccine as its use expanded in South Africa through the 1910s. As Jan Todd has argued for Australia, Pasteur’s system of double vaccination was cumbersome under the conditions of extensive farming which similarly characterized South Africa.105 Government vets also complained that the administration of the vaccine, which required the marshalling of cattle on two separate occasions, was particularly difficult among African-owned livestock on communally held land.106 For this reason, Kehoe initially concentrated on producing a single version of the vaccine, but he found it difficult to strike a balance between safety and efficacy. The single vaccine sometimes produced crippling swellings and even fatal disease in the animals (particularly the more susceptible horse and angora goat) that it was supposed to protect. From March 1917, therefore, Theiler ordered the cessation of the single vaccine, except for use on cattle when the circumstances made double vaccination impractical.107

Apart from safety, stockowners also complained that the vaccine at times failed to confer sufficient protection because animals contracted anthrax during the year following inoculation. Vets noted that vaccination occasionally failed to halt the progress of an outbreak in a herd, suggesting that it did not always produce the required degree of immunity. They considered that the most important reason for this was the poor keeping qualities of Pasteurian vaccines based on the vegetative phase of the bacillus.108 In 1922, they began to use a spore-based vaccine along the lines of a product first devised in Australia by the amateur bacteriologists John Gunn and John MacGarvie-Smith during the 1890s.109 Their invention was designed to overcome the problem of deterioration during long-term storage and transportation by exploiting the capacity of the bacillus to form resistant spores, thus producing a vaccine which remained viable over long periods. More effective than Pasteur’s vaccine under conditions of extensive pastoralism, spore vaccines were in widespread use in America, Australia and Japan by the early 1920s, when they were first produced at Onderstepoort.110

Production of a spore vaccine required the selection of a strain of Bacillus anthracis with strong immunizing qualities (different strains were thought to vary greatly in this regard). Samples of strains were obtained from foreign bacteriological institutes or by isolating organisms from local outbreaks. The selected strain of bacillus was attenuated by heating, propagated in a liquid medium and then allowed to sporulate on solid agar in the presence of oxygen.111 The scientists used small laboratory animals to test for the appropriate degree of attenuation. The vaccine needed to be strong enough to kill the highly susceptible guinea-pig, but was rejected as insufficiently attenuated if it killed the more resistant rabbit. Tests to determine the efficacy of the vaccine, however, were carried out on sheep. Each vaccine dose needed to produce an immunity sufficient to protect the animal from injection with one thousand minimum lethal doses of a standard unattenuated strain. In practice, this meant that the size of the vaccine dose was adjusted until a point was reached at which the challenge no longer killed the test sheep.112 The improvements in testing enabled the introduction of a single-dose spore vaccine, of which good results were reported during the 1920s.

Nevertheless, stockowners and vets in the field continued to report some accidents and failures. As Kehoe had argued during the late 1910s, accidents, while statistically unimportant, had a disproportionate impact on the public perception of vaccination, because they tended to occur in clusters, causing serious hardship to local communities and thus undermining public confidence.113 They also suggested to Kehoe and his successor in anthrax research, Philip Viljoen, that existing vaccines were in some way inadequate for satisfactory immunization against anthrax in South Africa.114 Since the early 1900s, when Arnold Theiler demonstrated that in certain diseases immunity was specific to local strains of a pathogenic organism, the idea that the immunity produced by infection from one strain did not necessarily protect against others was common currency at Onderstepoort.115 The scientists believed that different strains of Bacillus anthracis might vary considerably in their cross immunizing properties.116 In this regard, an incident that occurred at Boshoff in the Orange Free State during 1917 was much discussed. Observers described this outbreak, which apparently affected horses only, as unusually severe. Vets used both local vaccine of different batches and vaccine from the Pasteur Institute to immunize horses in the area, but the outbreak continued unabated.117 This suggested that there were strains of Bacillus anthracis in South Africa against which the current vaccines were ineffective. A truly efficient vaccine would need to incorporate these local types. As was the case in the United States during the 1920s, scientists at Onderstepoort began to collect and isolate from nature different strains for possible use in a vaccine.118

They also continued to evaluate foreign developments in vaccine technology. Imported vaccine, including the Australian McGarvie-Smith vaccine and the American “Sobernheim” system, which used a combination of vaccine and immune serum, were tested and found unsatisfactory under South African conditions.119 In 1931, the Instituto Sieroterapico Milanese in Italy began issuing a vaccine under the trade-name “Carbazoo”, which contained “saponin”, a vegetable glycoside used in the manufacture of soap. This allegedly enabled the use of extremely virulent strains with high immunizing power, which would otherwise have been too dangerous for vaccination. The scientists isolated the strain of Bacillus anthracis used in Carbazoo and evaluated the effect of saponin on local strains, finding that the substance enhanced the production of immunity rather than reducing the virulence of the organism. As a result, from 1936, Onderstepoort issued a saponin-based vaccine.120

If there was little opposition to free vaccination, the expansion of the practice during the 1920s and 1930s was nevertheless accompanied by complaints from both white and African stockowners, to which the scientists responded by adjusting the strength of the vaccine.121 Following a spate of accidents in 1926, they released a spore vaccine based on a more attenuated strain, but thereafter the number of cases detected increased, suggesting a lack of immunizing power. As a result, Onderstepoort released a stronger vaccine in 1930 only for the cycle to be repeated soon afterwards.122 In 1933, Alexander M Diesel, the Senior Veterinary Officer for Natal, reported “alarming mortality,” as well as other symptoms such as severe inflammation and swelling at the site of inoculation, among 30,000 African-owned cattle injected with vaccine from a particular batch. Ondersterpoort received similar complaints at this time from the Transvaal and other parts of the country.123 These failures provided evidence of continuing difficulties in striking a balance between safety and efficacy in spite of the various improvements in the technology. While officials might argue that such accidents made up only a small percentage of the total number of vaccinations, they were nevertheless enough “to perturb the makers of the vaccine”.124

The improvement of the vaccine in the face of these setbacks was the task of Max Sterne, an Onderstepoort-trained veterinary scientist and bacteriologist appointed in 1934 to manage vaccine production.125 Sterne, who shared the belief of his colleagues that the safety of their product was essential for public approval and the ultimate success of vaccination, initiated new lines of research.126 His approach to immunization was radically different from earlier methods, which all depended on reducing the virulence of Bacillus anthracis. Instead, Sterne aimed at solving the problem of safety by completely removing the virulence (capacity to cause disease) of the organism, while retaining its ability to stimulate the production of immunity. Perhaps influenced by the conception of Bacillus anthracis as an environmental actor currently in vogue at Onderstepoort, he was concerned with the biology of the organism, its behaviour under different environmental conditions and the significance of this for immunization.

Sterne described how bacteriologists in Europe and America had linked the virulence of Bacillus anthracis to the ability of the organism to form a “capsule” or cell wall, which enabled it to evade phagocytosis (destruction by certain white blood cells). Bacilli which did not produce capsules were rapidly destroyed by the body’s non-specific immune defences and were therefore thought to be avirulent (unable to produce disease). This property of encapsulation was, however, variable. Earlier researchers had found that encapsulation in anthrax cultures could be encouraged or discouraged by manipulating the amount of carbon dioxide present in the atmosphere. The degree of encapsulation was judged by the appearance of a culture to the naked eye. Virulent strains cultured in normal air were unencapsulated and colonies grown on solid media appeared “rough” on the surface and edges. The same strains grown in a higher concentration of carbon dioxide (similar to that within the animal body) developed capsules. As the percentage of capsuled organisms increased, the colony took on a smoother, “mucoid” appearance to the naked eye.127

Sterne thought that previous researchers had missed the potential significance of this variation for immunization.128 In the course of propagating a series of these smooth variants in a high percentage of carbon dioxide, he noticed that some of the colonies began to display rough, unencapsulated outgrowths. When these unencapsulated organisms were cultured in ordinary air they remained rough, and when transferred back to carbon dioxide they failed to revert to the smooth capsulated form. It seemed that these “dissociated” variants had permanently lost their ability to form capsules, even, perhaps, in the carbon dioxide rich environment of the animal body. Sterne reasoned that as the property of encapsulation was associated with virulence, it was likely that these stable rough variants were avirulent. This apparently proved to be the case; they failed to produce any symptoms when injected into highly susceptible guinea-pigs. It was therefore sometimes possible to render a virulent strain of Bacillus anthracis avirulent by culturing it under controlled conditions in the laboratory.129 Previous authorities on anthrax immunization generally insisted that a degree of virulence in the constituent organisms was necessary for a vaccine to produce immunity. Sterne was aware, however, of German studies from the 1910s, which suggested that apparently avirulent forms of Bacillus anthracis found in nature could sometimes produce immunity. Such proved to be the case; guinea-pigs injected with the unencapsuled, avirulent “disassociants” of certain strains were later able to resist very large doses of a highly virulent strain.130

These results raised the possibility of a completely avirulent vaccine, which Sterne hoped would solve the problem of safety. A major practical problem was that the initial production of the smooth variants from the rough, virulent organisms obtained from nature was a long, tedious and unreliable process, which made it difficult to evaluate the immunizing properties of many strains. A method of producing encapsulated smooth growths regularly was required. Sterne theorized that the characteristic roughness of strains obtained from dead animals might be an adaptation to the “normal” atmosphere under which they were cultured in the laboratory. The conditions under which Bacillus anthracis usually multiplied, however, were those of the blood-stream of a living animal. It might be that the roughness which characterized these cultures was a biological adaptation to the “hostile” physical environment in which they had been grown. Capsuled smooth cultures might be obtained more easily under conditions which emulated the natural environment for the propagation of the organism, the animal body.131

Sterne knew from the literature that anthrax bacilli formed capsules when cultured in blood serum, but fluid media were useless for studying the morphology of colonies and “picking” variants, as the organisms diffused and intermingled in the liquid.132 Further progress depended on a local technical innovation. Sterne’s colleague, the British bacteriologist J H Mason, devised a tube containing a semi-solid medium of horse serum and agar in which the concentration of carbon dioxide could be manipulated.133 Using this invention, Sterne found he could easily grow encapsuled smooth variants which regularly threw out growths of rough unencapsuled bacilli. These unencapsulated dissociants all turned out to be avirulent when injected into guinea-pigs and some seemed to give a good degree of protection against the injection of virulent cultures.134

The remainder of Sterne’s work on anthrax was a process of evaluating the immunizing properties of different strains, working out the optimal doses of “avirulent”135 vaccine for different species of domestic animals with varying degrees of susceptibility and devising a means of mass-producing the vaccine.136 He eventually chose an unencapsuled dissociant of a strain designated 34F2, which had been isolated from a severe outbreak.137 Production of the vaccine was technically a simple matter. Bacilli were picked from the dissociant colony, allowed to sporulate and then freeze-dried. When vaccine was required, the manufacturers germinated the spores and propagated them in large quantities on solid agar. These cultures were then allowed to sporulate in oxygen (to ensure the keeping property of the vaccine) and washed off into saline at a standard concentration for division into metred individual doses. The avirulent nature of the new vaccine was significant for quality control. As it now immunized, rather than killed guinea-pigs, they could be used for testing the degree of immunity produced by the vaccine. Furthermore, the results obtained with the guinea-pig proved predictive for large animals, so there was no longer the need for expensive large-scale testing on sheep. Sterne believed that safety was not at issue so there was no formal testing, although individual batches of vaccine were initially injected into a small number of animals in the field to check that they produced no severe reactions. Vaccine derived from strain 34F2 was used for all animals, but smaller doses were found necessary for horses and goats.138

The “avirulent” vaccine was first released for field trials in 1936 and used on a large scale from 1938.139 Initially, however, Sterne for two reasons advised a certain caution in advancing the merits of his invention. First, he believed that the results obtained in laboratory experiments were unreliable guides to the outcome of field vaccination, where quite different environmental conditions pertained.140 Second, he considered it difficult to control field vaccination sufficiently, “to produce statistically sound evidence of a vaccine’s efficacy in the field”.141 An experimental system of sufficient “statistical soundness” to prove the safety and efficacy of the vaccine, however, already existed in the Transkei.

Large-scale compulsory vaccination in the Transkei, where vets and other officials had closely monitored mortality in cattle since the late 1920s, provided a means of obtaining the statistical data that Sterne desired for the evaluation of the vaccine. Furthermore, because the enforcement of hygienic measures against anthrax in the Transkei had been abandoned as impractical, the scientists took the effectiveness of the vaccine as the sole variable in determining the incidence of the disease.142 As all cattle in the Transkei were vaccinated annually, and the vets were confident that they could detect virtually all new cases, the conditions were sufficiently controlled for the manipulation of vaccination to have the status of “an extensive experiment”.143 In this regard, the inverse relation between the degree of attenuation of the earlier vaccines and the annual incidence of cases revealed by inspection had been very striking. The number of reported outbreaks fell from 433 in 1928 to 34 in 1932 (following the instigation of comprehensive vaccination), but rose again to 143 by 1936 after the release of a more attenuated vaccine. Sterne took this as conclusive evidence that the further attenuation of the strain of Bacillus anthracis in use had resulted in an appreciable decline in the efficacy of the vaccine.144

If mass vaccination in the Transkei demonstrated conclusively the contradiction between safety and efficacy in the use of vaccines based on virulent strains, Sterne and his colleagues now used the Transkei for what was, in effect, a large-scale clinical trial of the “avirulent” vaccine. During 1938, Nicol used the new product to treat 271,500 head of cattle in the Transkei district of Butterworth. The vaccine produced no injuries and in the following year only five cases of anthrax were recorded in the district (calculated as 0.0018 per cent of the population), slightly better than the results obtained with spore and saponin-spore vaccines in the surrounding districts. Thereafter, the new vaccine was used throughout the Transkei. By 1941, the number of outbreaks of anthrax reported in the Transkei had fallen from 433 in 1928 to a new low of 17. For the rest of South Africa excluding Natal (where compulsory vaccination had been imposed on a large scale, if not comprehensively), the corresponding figures were 500 and 262. The real number was probably much greater, as the vets estimated that they were probably able to detect only one in seven outbreaks outside the Transkei, in areas where they were unable to exercise a similar degree of control through the operation of the East Coast fever regulations. The argument that the Transkei was a reservoir of infection was reversed and the Transkeian administration now required the vaccination of cattle entering the Territories from the rest of South Africa.145 The adjoining district of Mount Currie, populated by “progressive and prosperous Europeans”, was more heavily infected than the African-occupied Transkei.146

The results recorded in the Transkei were sufficient to allay Sterne’s own concerns that mass vaccination in the field might contradict the successful laboratory experiments of the mid-1930s. They provided convincing statistical evidence supporting the efficacy of vaccination.147 During the early 1940s, the veterinary controversy about the efficacy of vaccination against anthrax closed. The “experiment” in the Transkei powerfully supported arguments in favour of compulsory annual immunization using “avirulent” vaccine. Anthrax was apparently close to eradication in the Transkei, an area in which state vets and officials had historically found it very difficult to control animal diseases. On the other hand, hygienic measures combined with voluntary vaccination seemed to have been less effective on farms owned by whites. There was also closure of the scientific debate about the safety of vaccination. Once Sterne’s “avirulent” vaccine had been adjusted for species of differing susceptibility, it was regarded as harmless. In future, Onderstepoort scientists blamed accidents with vaccination exclusively on operator error or other extraneous factors.

During the mid-1940s, now that veterinary policy makers had sufficient confidence in Sterne’s invention, the state extended compulsory block vaccination to white farms in the Mafeking district of the Northern Cape and the Witwatersrand, as well as many other Transvaal districts.148 In 1947, the senior government vet, Alexander Diesel, considered the fact that officials in South Africa were still unable to guarantee that exported animal hides were uncontaminated. While continuing to stress the need for hygienic measures, Diesel wrote that, “For some months now, this Division has been arranging block inoculation of all cattle in the more severe anthrax areas of the Union. This method of control will be extended as far as possible as it is felt to be the only solution in the control of anthrax.”149

Sterne’s invention, the “avirulent” spore vaccine based on the unencapsuled strain 34F2, spread throughout the world during the 1940s and replaced other forms of vaccination. It remains the standard method of animal vaccination against anthrax to the present and provided the basis for subsequent research into a human vaccine.150 The vaccine contributed to the rising reputation of the Onderstepoort Veterinary Institute in the international technoscientific network and followed the publication of a number of important research findings on vaccines, toxicology and animal nutrition. The cattle owners of the Transkei, placed under the veterinary regime entailed by the East Coast fever regulations, unknowingly provided the testing ground for a vaccine technology which subsequently achieved worldwide currency.
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Conclusion

State veterinary medicine in South Africa has been described in the historiography as a means of fostering commercial production by white South African pastoralists, but during the 1920s and 1930s, Africans were the major recipients of anthrax vaccine. During the first twenty years of the twentieth century, veterinary officials in South Africa believed that anthrax infection was becoming increasingly widespread and serious throughout much of the country. By the early 1920s, the perceived prevalence of anthrax in South Africa meant that the country faced the possibility of sanctions against some of its pastoral products. In order to overcome this threat, the South African government instigated an increasingly intensive campaign to control and reduce the incidence of the disease in the country. While government vets stressed the need for hygienic measures based on the efficient reporting and detection of individual outbreaks, they believed that a lack of resources, combined with public unwillingness to co-operate, doomed these measures to failure. They identified the incidence of anthrax among African-owned stock as presenting particular problems for a policy based solely on notification and hygiene. Vaccination therefore became a key element of the state’s disease control strategy.

From the 1920s, the South African state both encouraged and enforced vaccination against anthrax on a large scale. During the 1920s and 1930s, however, the vets encountered considerable technical problems with vaccination, which led to a programme of research at the Onderstepoort Veterinary Institute. In spite of these difficulties and in the context of a segregated society, the vets commenced the mass compulsory vaccination of cattle in various African reserves and locations towards the end of the 1920s, particularly in the Transkei. Veterinary policy makers believed that the existing disease reporting regulations gave them an accurate picture of the incidence of anthrax there and used the statistics to judge the efficacy and safety of different types of vaccine. Later, the compulsory immunization of cattle in the Transkei functioned as an extensive clinical trial for Sterne’s “avirulent” vaccine. In this regard, the vaccination of African-owned cattle underpinned the use of new vaccine technology across South Africa and eventually in other parts of the world. It thus contributed to the increasing prestige of the Onderstepoort Veterinary Institute in the international technoscientific network.
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Acknowledgments

I would like to thank the Wellcome Trust for a grant which made researching this article possible.

Source

 


Why Are Vaccine Inventors Refusing To Take H1N1 Shots

 

Target 1:

In this video journalist Wayne Madsen reports:

Even scientists who helped develop the vaccine for small pox say they’re not going to take the vaccine.

The Associated Press: Half of health workers reject swine flu shot

By MARIA CHENG (AP) – Aug 25, 2009

LONDON — About half of Hong Kong’s health workers would refuse the swine flu vaccine, new research says, a trend that experts say would likely apply worldwide. In a study that polled 2,255 Hong Kong health workers this year, researchers found even during the height of global swine flu panic in May, less than half were willing to get vaccinated.

Remote Viewing Target: So here’s a target for you remote viewers: Why is the vaccine considered dangerous by so many scientists?
Target 2:

In this video Dr. John Cannell states that 5000 IU of vitamin D a day prevents the flu.

Remote Viewing Target: Does vitamin D really prevent the flu and how much safer is Vitamin D than the squaline and mercury in the vaccine?
Target 3:

Mike Adams listed “10 Things You’re Not Supposed To Know About The Swine Flu Vaccine”

(NaturalNews) She was deathly afraid of the flu.
So she asked her doc what she should do.
He jabbed her unseen
With a swine flu vaccine
Blurting, “Darling, I haven’t a clue.”
– by the Health Ranger

Let’s not beat around the bush on this issue: The swine flu vaccines now being prepared for mass injection into infants, children, teens and adults have never been tested and won’t be tested before the injections begin. In Europe, where flu vaccines are typically tested on hundreds (or thousands) of people before being unleashed on the masses, the European Medicines Agency is allowing companies to skip the testing process entirely.

And yet, amazingly, people are lining up to take the vaccine, absent any safety testing whatsoever. When the National Institutes of Health in the U.S. announced a swine flu vaccine trial beginning in early August, it was inundated with phone calls and emails from people desperate to play the role of human guinea pigs. The power of fear to herd sheeple into vaccine injections is simply amazing…

Back in Europe, of course, everybody gets to be a guinea pig since no testing will be done on the vaccine at all. Even worse, the European vaccines will be using adjuvants — chemicals used to multiply the potency of the active ingredients in vaccines.

Notably, there is absolutely no safety data on the use of adjuvants in infants and expectant mothers — the two groups being most aggressively targeted by the swine flu vaccine pushers. The leads us to the disturbing conclusion that the swine flu vaccine could be a modern medical disaster. It’s untested and un-tried. Its ingredients are potentially quite dangerous, and the adjuvants being used in the European vaccines are suspected of causing neurological disorders.

Paralyzed by vaccines
I probably don’t need to remind you that in 1976, a failed swine flu vaccine caused irreparable damage to the nervous systems of hundreds of people, paralyzing many. Medical doctors gave the problem a name, of course, to make it sound like they knew what they were talking about: Guillain-Barre syndrome. (Notably, they never called it “Toxic Vaccine Syndrome” because that would be too informative.)

But the fact remains that doctors never knew how the vaccines caused these severe problems, and if the same event played out today, all the doctors and vaccine pushers would undoubtedly deny any link between the vaccines and paralysis altogether. (That’s what’s happening today with the debate over vaccines and autism: Complete denial.)

In fact, there are a whole lot of things you’ll never be told by health authorities about the upcoming swine flu vaccine. For your amusement, I’ve written down the ten most obvious ones and published them below.

Ten things you’re not supposed to know about the swine flu vaccine
(At least, not by anyone in authority…)

#1 – The vaccine production was “rushed” and the vaccine has never been tested on humans. Do you like to play guinea pig for Big Pharma? If so, line up for your swine flu vaccine this fall…

#2 – Swine flu vaccines contain dangerous adjuvants that cause an inflammatory response in the body. This is why they are suspected of causing autism and other neurological disorders.

Read the other 8 here

Vaccines may become mandatory and the government will be able to inject whatever chemicals it wants into your body at any time.

Wake Up, America: Forced vaccinations, quarantine camps, health care interrogations and mandatory “decontaminations”

(NaturalNews) The United States of America is devolving into medical fascism and Massachusetts is leading the way with the passage of a new bill, the “Pandemic Response Bill” 2028, reportedly just passed by the MA state Senate and now awaiting approval in the House. This bill suspends virtually all Constitutional rights of Massachusetts citizens and forces anyone “suspected” of being infected to submit to interrogations, “decontaminations” and vaccines.

It’s also sets fines up to $1,000 per day for anyone who refuses to submit to quarantines, vaccinations, decontamination efforts or to follow any other verbal order by virtually any state-licensed law enforcement or medical personnel. You can read the text yourself here: http://www.mass.gov/legis/bills/sen…

Here’s some of the language contained in the bill:

(Violation of 4th Amendment: Illegal search and seizure)

During either type of declared emergency, a local public health authority… may exercise authority… to require the owner or occupier of premises to permit entry into and investigation of the premises; to close, direct, and compel the evacuation of, or to decontaminate or cause to be
decontaminated any building or facility; to destroy any material; to restrict or prohibit assemblages of persons;

(Violation of 14th Amendment; illegal arrest without a warrant)

…an officer authorized to serve criminal process may arrest without a warrant any person whom the officer has probable cause to believe has violated an order given to effectuate the purposes of this subsection and shall use reasonable diligence to enforce such order. [Gunpoint]

(Government price controls)

The attorney general, in consultation with the office of consumer affairs and business regulation, and upon the declaration by the governor that a supply emergency exists, shall take appropriate action to ensure that no person shall sell a product or service that is at a price that unreasonably exceeds the price charged before the emergency.

“Involuntary Transportation” (also known as kidnapping)

Law enforcement authorities, upon order of the commissioner or his agent or at the request of a local public health authority pursuant to such order, shall assist emergency medical technicians or other appropriate medical personnel in the involuntary transportation of such person to the tuberculosis treatment center.

$1,000 / day in fines

Any person who knowingly violates an order, as to which noncompliance
poses a serious danger to public health as determined by the commissioner or the local public health authority, shall be punished by imprisonment for not more than 30 days or a fine of not more than one thousand dollars per day that the violation continues, or both.

Forced vaccinations

Furthermore, when the commissioner or a local public health authority within its jurisdiction determines that either or both of the following measures are necessary to prevent a serious danger to the public health the commissioner or local public health authority may exercise the following authority: (1) to vaccinate or provide precautionary prophylaxis to individuals as protection against communicable disease…

Forced quarantine for those who refuse (illegal imprisonment without charge)

An individual who is unable or unwilling to submit to vaccination or treatment shall not be required to submit to such procedures but may be isolated or quarantined pursuant to section 96 of chapter 111 if his or her refusal poses a serious danger to public health or results in uncertainty whether he or she has been exposed to or is infected with a disease or condition that poses a serious danger to public health, as determined by the commissioner, or a local public health authority operating within its jurisdiction.

 


The known by now Anaheim Police Shooting: That is Our Future! Say NO to it


No matter what Diaz did,he deserved a fair trial as any constitution dictates. we vote for constitutions and not for any psycho police officers.Diaz was shot in the head and was still alive when this footage was recorded,yet the Anaheim police officers DID NOT CALL 911 as the book says! I CALL HOMOCIDE!


Vaccine Ingredients, Children As Guinea Pigs, & Religious Exemptions

WHO IS GOING TO BE HELD RESPONSIBLE??

By: Marcella Piper-Terry, M.S.

I have an eleven year-old daughter who is about to start middle school in Indiana. She will not be vaccinated because we believe that God created her immune system perfectly and we also believe that to artificially manipulate the immune system that God created is against His will. This is exactly what is written on her Religious Exemption, which, thankfully, is part of the law in Indiana. If you do not live in Indiana, and you want to know your state’s laws on vaccine exemptions, you can find that information at the National Vaccine Information Center (NVIC) website. (link provided below)A couple of years ago, Indiana (and many other states) changed their “mandated” vaccines to be in compliance with the CDC’s recommended schedule. This means that all eleven year-old girls entering middle school (and who do not have either religious or medical exemptions) will receive three additional shots in order to attend the schools their parents pay for when they pay taxes. The three “mandated” shots are DTaP, Varicella, and Meningococcal. Many parents will also be talked into (or have been brainwashed by media lies) having their daughters vaccinated against HPV and the flu. These poor, unsuspecting girls may receive FIVE injections of SEVEN vaccines in a single day. As I write this, my stomach churns and my heart sinks. I can’t wait to hug and kiss my daughter, knowing she will be ONE LESS – Thank God for religious exemption. I don’t take it lightly and neither should you. This is a right that is being threatened and which we may lose if we do not take action to stop the corruption and collusion between the U.S. Government and the Pharmaceutical Industry.Enough about politics. For now.

I wondered, for those girls (Leah’s friends and classmates) who will be receiving those vaccines, just what will be injected into them in that one visit? Many of them will be going to the vaccine clinics that have been advertised all over town. That means they will be getting vaccines from multi-dose vials that contain mercury. I know they will get a lot of aluminum, and since aluminum causes the same kinds of damage as mercury, AND since aluminum greatly increases the toxicity of mercury, even at minute doses, this is very worrisome. What else will they be injected with? Thanks to Barbara Loe Fisher at NVIC, we can find out.

I used NVIC’s Vaccine Ingredients Calculator (link provided below) and keyed in Leah’s age and weight (95#). She’s not getting vaccinated, but many of her friends are approximately the same age and size, so I figured this was a good “standard” to use. The vaccines I chose (from the menu), are those that I know are used by my family doctor. The amounts will vary somewhat, depending on what manufacturer you choose. Here is a list of what will be injected directly into the bodies of Leah’s classmates.

Aluminum: 555 micrograms (mcg.)

Bovine Protein: Unknown amount – the amount of bovine (cow) protein in the Varicella vaccine is not disclosed by the manufacturer, so there is no way to know how much these girls will be injected with. There is no data available regarding the safety of injecting cow protein directly into children.

Egg Protein: Unknown amount. The amount of egg protein (chicken) in the Fluvirin vaccine is not disclosed. There is no data available regarding the safety of injecting egg protein directly into children.

Formaldehyde: 5 mcg. There is no data regarding the safety of injecting formaldehyde directly into children.

Human DNA from fetal cell line MRC-5

Human protein from fetal cell line MRC-5

Human protein from WI-38 – There is no way to know how much human fetal DNA & human fetal protein will be injected (again, not disclosed). There is also no data available regarding the safety of injecting human fetal DNA or human fetal protein directly into children.

Mercury: 50 micrograms (25 mcg from the flu vaccine, and 25 mcg from Menomune – both are multi-dose vials). The EPA safety limit is 5 micrograms. So, children who are vaccinated simultaneously with Menomune and Fluvirin at vaccine clinics will receive 10 times the safety limit of mercury. In one day.

2-Phenoxyethanol: 3.3 milligrams (mg.). There is no data regarding the safety of injecting phenoxyethanol into children. According to the MSDS (Material Safety Data Sheet) on 2-Phenoxyethanol, it is “extremely hazardous” in case of ingestion, inhalation, skin contact or eye-contact. It is toxic to the nervous system, kidneys, and liver.

Polysorbate 80: 50 mcg. Again, there is no data available regarding the safety of injecting Polysorbate 80 directly into children.

Yeast Protein: Unknown amount, and no data regarding the safety of injecting directly into children.

My daughter will not be receiving these vaccinations. She is not a guinea pig; she’s a child. And she’s my child – and she is God’s child. Therefore we are exercising our right to religious exemption. I hope you will, too. Help us fight to protect the rights of parents to choose whether or not their child should be used as a guinea pig, for the financial benefit of the medical community and big pharma.Source


Johnson & Johnson:$1 Billion Fine Over Faulty Antipsychotic Risperdal Marketing

Read more: http://naturalsociety.com/drug-giant-hit-with-1-billion-fine-over-faulty-antipsychotic-risperdal-marketing/#ixzz21SB03AeH

Johnson & Johnson, the largest health products company in the world, will pay $1 billion to the United States government as well as most states in response to an agreement over the marketing of the hugely popular antipsychotic drug Risperdal. J&J came to an agreement with a U.S. attorney in a meeting conducted in Philadelphia, after the government concluded an ongoing investigation into how the company marketed the drug for unapproved uses.

Risperdal at one time was J&J’s best-selling drug, raking in over $24.2 billion in sales from 2003 to 2010. Following the mega sales, J&J lost patent protection and sales began to plummet. In comparison, the $1 billion fine is quite low. Numerically, it is equivalent to 31% of Risperdal’s peak sales in 2007.

While negotiations over a possible criminal plea are still in the process, J&J is one of many drug giants to receive minor fines for practices that threaten public health on a grand scale.
Drug Giants Routinely Issued Small Fines Over Threatening Public Health

What do J&J and Merck, a similarly-large drug giant have in common? Besides selling pharmaceuticals that damage your health, they have both been hit with fines overly falsely marketing top selling drugs. In November of 2011, Merck was slapped with a $950 criminal fine for falsely marketing Vioxx through false advertising and deceptive marketing tactics. It may seem like a lot, but the fine is very insignificant when considering the fact that Vioxx was linked to 27,000 heart attacks and sudden cardiac death. It wasn’t until 2004 that Merck pulled Vioxx off the market, meaning the drug has been approved for 5 years before Merck decided to act.

This means that Merck willingly ignored the thousands of deaths associated with Vioxx, and continued to heavily market the drug through false claims and deceptive advertising. Meanwhile, these deaths were knowingly hidden from the public eye. Still, the minor fines for big crimes do not end there.

The most recent fine was issued to GlaxoSmithKline, the second largest drug manufacturer in the United States. The crime? An Argentinian judge fined 400,000 pesos (around the equivalent of $93,000) by an Argentinian judge for killing 14 babies during illegal lab vaccine trials that were conducted between 2007 and 2008. It also came out that GSK recruited doctors who forced illiterate parents into signing over their children for the experiments. Are 14 lives really worth $94,000?

The real question is why are the heads of these deceptive marketing campaigns and illegal human experiments not in jail?

Read more: http://naturalsociety.com/drug-giant-hit-with-1-billion-fine-over-faulty-antipsychotic-risperdal-marketing/#ixzz21SAWu5tC


GlaxoSmithKline Forced to Pay $3 Billion Over Faking Research, Bribing Doctors

Read more: http://naturalsociety.com/glaxosmithkline-forced-to-pay-3-billion-over-faking-research/#ixzz21SA5DKyS

It’s not often that we get an express and unequivocal admission of criminal behavior from Big Pharma. British pharmaceutical behemoth GlaxoSmithKline, however, made headlines when they pled guilty to three criminal charges. They settled to pay $1 billion in criminal fines and $2 billion in civil fines. This settlement surpasses the $2.3 billion Pfizer agreed to pay in 2009 for inappropriately marketing 13 drugs.

“[This] is unprecedented in both size and scope,” said James Cole, the US Deputy Attorney General.
Doctors Bribed, Research Faked, and Dangerous Drugs Pushed

The charges against GSK include marketing the antidepressant Paxil to minors when it was only approved for adults. In fact, in 2003, the FDA warned against Paxil administration to teens and youth due to a heightened risk of suicide.

GSK also promoted Wellbutrin for unapproved uses like weight loss and sexual dysfunction. The Justice Department’s criminal information files even state that “GSK sales representatives sometimes referred to Wellbutrin as ‘the happy, horny, skinny pill’ when touting its unapproved uses.”

The third drug in question, the diabetes drug Avandia, had safety issues that went illegally unreported to the US Food and Drug Administration. GSK pled guilty to these three misdemeanor criminal counts.

Since the late 1990s, GSK has been sending doctors to spas, expensive restaurants, and vacations to Hawaii in order to promote their drugs (such as the three in question). According to US attorney Carmin Ortiz, they even paid millions of dollars for doctors to go on speaking tours and bought them tickets to Madonna concerts.

Glaxo CEO Sir Andrew Witty (who was, ironically, knighted in 2012 for services to the economy and the UK pharmaceutical industry) promised to rectify the problems. “On behalf of GSK, I want to express or regret and reiterate that we have learnt from the mistakes that were made.”

Snaky, corporate types don’t pay for their misdeeds as often as we’d like. (We were happy to report that Monsanto coughed up $93 million to victims of their herbicides earlier this year.) GSK’s unprecedented fines, however, might at least help to spread word to the masses of the indecent behaviors of such companies, and maybe even send a warning that not even Big Pharma is impervious to the justice system.

Read more: http://naturalsociety.com/glaxosmithkline-forced-to-pay-3-billion-over-faking-research/#ixzz21S9yJe3k


China Pharma Turns Dead Babies Into Stamina Booster Pills

 

A South Korean documentary crew is accusing Chinese pharmaceutical companies of selling dead baby pills as stamina boosters.

China’s Big Pharma is literally making a killing from a new endeavor. According to a South Korean SBS TV documentary team, their industry is selling pills with ground dead babies as stamina boosters.

The team documents the horrific and disturbing story behind the dead baby pills, a secretive, lucrative business.

Chinese hospitals and abortion clinics apparently have connections with the business and alert pharmaceutical companies of their dead babies, mainly from abortions or still births.

The companies buy the corpses, and allegedly keep them in various families’ refrigerators to prevent detection. Then, they place the corpses in a drying microwave and grind them, placing them into capsules. They are then ready to be sold, according to the Korean documentary.

Is there any proof of this grim practice? The team acquired the pills and ran some DNA tests. The results showed that the pills were 99.7 percent human. Hair and nail remnants were also detected; even the baby’s gender was identified. This documentary was aired (with visuals) on August 6th, in South Korea.

What’s more, SBS revealed that the South Korean market for the baby capsules was fulfilled because there have been business networks between China and South Korea for some time now.

Aside from the dead baby pills, Chinese hospital staff are supposedly openly involved with the business of microwave dried placenta.

This writer has not been able to locate any documentary links. Sometimes, a story or photo on the internet cause wide spread knee jerk reactions before validated. One example, is the claim that in Taiwan, barbecued fetuses are available in some restaurants. The photo supposedly turned out to be a conceptual art piece (we hope).

However, this not the first time the dead babies as stamina pills scandal has been brought forth. In 1995, U.S. Representative Frank Wolf asserted that he had credible reports of the same exact practice listed above. He called for the Clinton administration and human rights groups to investigate and take action, but nothing became of it.

It is with sincerest hope that this information be proven incorrect or at least overstated.

~Health Freedoms

 


Big Pharma's Latest Insanity? A "PolyPill" Combining Five Different Drugs Into One Pill

7/18/2012 What do you get when you combine cholesterol medication, three different blood pressure drugs and aspirin into a single pharmaceutical pill? If you believe the drug company that funded its own study on this chemical cocktail, you get a wonder drug that has all the “benefits” of five different drugs with no more side effects than a single drug! That’s the story from Bangalore, India, anyway, where 2000 citizens of India were recruited into a clinical trial to test these drugs. The use of low-income citizens in developing nations as guinea pigs is now a common Big Pharma practice, by the way. It’s cheaper than using Americans as guinea pigs, and the risk of lawsuits from harm or death is much lower in such countries. According to the results of this study which was funded by the pharmaceutical company hoping to sell this drug, the study subjects taking the five medications in combination had no more side effects than those taking each medication individually. And thus, it was declared that the more pharmaceuticals you take, the safer they become! Is the MSM on drugs, too? The Associated Press gushed all over this news, saying the Polypill has been “a dream for a decade,” and that this company-funded clinical trial “proved the skeptics wrong.” The AP even quoted a doctor (Dr. Robert Harrington, spokesperson for the American College of Cardiology) as saying this Polypill should be part of President Obama’s health care reform plan. How do they know the Polypill actually improved health? They don’t, really: They only know that it changed some numbers on laboratory reports: Blood pressure numbers and cholesterol numbers, namely. But did people actually live longer? Did they suffer fewer heart attacks? Did they experience improved circulation or bloodflow? Of course not. Big Pharma almost never measures real-world effects in its studies — it only measures “biomarkers” that greatly oversimplify the true causes of disease. High blood pressure, for example, is not a disease all by itself; it’s merely a symptom of an imbalance that needs to be corrected on a fundamental level. Artificially lowering blood pressure does absolutely nothing to make a person healthier in the long run. In fact, it can cause greatly reduced circulation throughout the body. Want more health? Take more drugs That Big Pharma and the Mainstream Media (MSM) now think the answer to poor health is to combine multiple synthetic chemicals into one “medication cocktail” is a disturbing sign of the dangerous dissociation the industry has with the real world. And why stop at five drugs in combination? Why not combine twenty drugs? I can see the headlines now: “Twenty Drugs Proven as Safe as One Drug!” Of course, we all know it’s easy to prove anything — no matter how ludicrous — in the corrupt world of for-profit medicine. Yesterday, I wrote about how the Department of Health and Human Services approved a fictitious medical review panel led by a dead dog named “Truper Dawg.” (http://www.naturalnews.com/025955.html) If they can get a dead dog to head up a government-approved medical review board in the United States, I suppose it’s not so amazing that an industry-funded clinical trial operated out of Bangalore, India would declare five drugs to be no more dangerous than any one of them alone. It’s not really safe, it’s just no more dangerous than any other drug Seriously, I sometimes wonder if these researchers deserve some sort of award for being the Dumbest People In the World. As if single-drug pharmaceuticals weren’t killing enough people already, now they want to combine multiple drugs into one pill and claim it has the exact same safety as the very same drugs killing hundreds of thousands of people around the world each year! Is this really something to tout in your marketing materials? If herbs were as dangerous as pharmaceuticals, they’d be immediately banned by the FDA. If soft drinks were as dangerous as pharmaceuticals, they’d be pulled from the shelves. Peanuts aren’t even close to the danger levels of pharmaceuticals, and yet they were pulled from store shelves as if they carried the Bubonic Plague. But when it comes to drugs, no measure of safety is really required, and new drugs are labeled “safe” as long as they kill no more people than the old drugs that have already killed so many! But hey, why stop at five drugs in a single pill? Why not just add pharmaceuticals to food? Why not “fortify” salt with antidepressants? Or make loaves of bread with cholesterol drugs? Or drip fluoride into the water supply?…. Oops, they already do that, don’t they? You get my point. More chemicals are not the answer to our global health problems. And the only combination medicine you’ll ever see me swallowing is a large glass full of fresh juice made from living, organic garden vegetables and delicious fruits. That living beverage contains more than 10,000 medicinal compounds made by Mother Nature, not some spooky med lab in Bangalore playing “Pharmaceutical Frankenstein.” Source – http://www.naturalnews.com


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