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http://www.ioa.com/~dragonfly/vaccine2.html
The Forty Year Legacy of Tainted Polio Vaccine
by
Harold Stearley
In the late 1940's and early 1950's the polio virus was taking a savage toll on the
American public. Thousands of children and adults were crippled or killed. In 1955, Jonas
Salk performed a medical miracle when he discovered how to mass produce polio vaccine by
growing it on the kidneys of rhesus monkeys. While there is no question that thousands
were saved from the ravages of polio by the Salk vaccine, by 1960 a problem had surfaced
-- a problem which would come back to haunt the nation some forty years later.
The complication researchers had isolated in 1960 was a viral contaminate. It seems that
when the live polio virus grown on monkey tissues was extracted for vaccine production
another virus was extracted as well, SV-40. When this monkey virus was injected into
research animals it produced brain cancer. It appears our government didn't wish to create
a public panic or discredit the public health service, because instead of recalling the
tainted vaccines, it quietly ordered the manufacturers to find a monkey free of SV-40 and
continue production. As of 1963, the rhesus monkey had been replaced with the African
green monkey for production of a safer polio vaccine, but between the years of 1955 and
1963 as many as 98 million Americans had received doses of live polio virus vaccines
tainted with SV-40.
Jumping to the early 1990's, Michele Carbone, Assistant Professor of Pathology at Loyola
University in Chicago, isolated fragments of the SV-40 virus in human bone cancers and in
a particularly nasty form of lung cancer called mesotheliomas. The viral contaminate from
the 50s was back to haunt us, and appeared in 33% of the osteosarcoma bone cancers
studied, in 40% of other bone cancers, and in 60% of the mesotheliomas lung cancers. Dr.
Carbone believed this study could explain why 50% of the current mesotheliomas being
treated were no longer occurring in association with their traditional cause of asbestos
exposure.
Already sounding like a bad science fiction story, the worse news was yet to follow. An
Italian team of researchers from the Institute of Histology and General Embryology of the
University of Ferrara lead by Dr. Fernanda Martini discovered SV-40's presence in various
other tumors.
To be specific they found the monkey virus in 83% of choriod plexus papillomas, in 73% of
ependymomas, in 47% of astrocytomas, in 50% of glioblastomas, and in 14% of meningiomas.
While the virus's appearance in all of these types of brain tumors is mortifying, even
more so is the fact that it materialized in 23% of blood samples and 45% of sperm fluids
taken from normal individuals -- normal meaning free of disease at the time of testing.
The researchers determined the virus could be transmitted sexually and through blood
transfusions. As if to drive this point home, SV-40 has appeared in 61% of all new cancer
patients -- patients too young to have received the contaminated vaccine being
administered forty years ago who are now believed to have been infected by human to human
transmission. Being a blood born organism, it is also suspected that SV-40 is
transmissible from mother to child during pregnancy.
The more this matter is researched the more startling the evidence. Senior epidemiologist
at the National Institutes of Health, Dr. Howard Strickler, has plotted a geographic
pattern to the cancers associated with SV-40 helping to confirm its link to the tainted
vaccine. People who lived in Massachusetts and Illinois who received identified lot
numbers of the contaminated vaccine administered in the 1950s are now demonstrating ten
times the rate of the osteosarcoma bone tumors as those who received vaccine free of the
SV-40 contaminate in other parts of the country.
The Food and Drug Administration (FDA) mandates that every American infant and child
receive polio vaccinations. While public health officials continue to emphasize how
current supplies of the vaccine are safe, Peter Reeve, FDA Virologist, has acknowledged
that the administration abandoned independent testing of vaccine purity some fifteen years
ago. The job of ensuring safety and purity rests squarely on the shoulders of those
manufacturing the vaccines with no federal oversight. Wyeth-Lederle controls the supply of
all the oral polio vaccine in this country, and last year's sales totaled some $230
million dollars. Surely there would be no conflict of interest in allowing this
corporation to be the sole agent of quality oversight of their own pocketbook?
The government may not have paid attention to the quality of these vaccines, but they had
formulated a plan for their distribution. Federal vaccination policy advocated the use of
live-virus oral polio vaccine (OPV) based on the belief the live virus shed in the body
fluids of infants immunized with OPV could immunize others through contact exposure. The
Centers for Disease Control (CDC) insisted this was a safe practice, and emphasized that
no one previously vaccinated could contract the disease in this manner. The public was
never informed of this strategy, however, and no consent was ever obtained from the
unknowing participants in this vaccination scheme. One hundred and twenty people, many
previously vaccinated, contracted polio as a result of this practice. To add insult to
injury in 1994 the World Health Organization proclaimed polio was eliminated from the
Western Hemisphere. Insult because for the past seventeen years the only cases of polio
occurring in the United States have been caused by the vaccine itself, and injury because
this victory will be paid for in blood from the cancers produced by the monkey virus
spread with the vaccine.
One might ask just how such a thing could happen considering the injectable form of the
vaccine (IPV) does not use a live virus and doesn't transmit the disease it is designed to
shield us from? Well, Wyeth-Lederle's leading competitor Connaught produces IVP which
could explain why Wyeth lobbied so hard against the CDC recommending increased use of IVP.
In 1996 the CDC revised its recommendation from four doses of OPV to two doses of IVP
followed by two doses of OPV, however, physicians have been instructed to give all four
doses as OPV if they desire. The cost of IVP vaccine is $5.40 per dose, whereas OPV costs
$2.32 per dose. With the difference in cost favoring the use of OPV, and the current
climate of regulating health care costs, clearer guidelines must come from the government
if they truly expect to increase the use of the safer IVP vaccine.
Well the story of contaminated polio vaccine is not over yet. Microbiologist Howard
Urnovitz, Ph.D. provided significant evidence at the Eighth Annual Houston Conference on
AIDS that human immunodeficiency virus type 1 (HIV-1) is a monkey hybrid virus which was
produced when 320,000 Africans were injected with polio virus contaminated with live
simian immunodeficiency virus (SIV) in the late 1950's. Apparently, viral fragments
combine easily with other viruses to produce these hybrids called "chimeras."
This theory was confirmed by another research team headed by Dr. B. F. Elswood at the
University of California in San Francisco. Interestingly enough, when researchers Cecil H.
Fox and John Martin applied to the National Institutes of Health for grants to confirm the
presence of SIV and simian cyto-megalovirus (SCMV) contaminates in polio vaccines their
requests were denied. Dr. Urnovitz may have an explanation as he stated in the Boston
Globe, "that almost 100 million Americans were exposed (to SV-40) through a
government sponsored program, but for over 30 years, there has been virtually no
government effort to see if anyone's been harmed by the exposure." He added,
"The government will not fund science that makes it look culpable."
Could it be our government, once again, is attempting to avoid a public panic while
ignoring the great potential for harm these viruses could inflict. Time will tell. Harvard
Medical School professor, Dr. Ronald Desroier points out that taking all known scientific
evidence into account that the medical experts' knowledge is limited to "perhaps 2%
of existing monkey viruses." Who knows what lethal virus may be discovered in our
blood streams forty years from now as a result of good intentions....
References
Berleur, M. P., & Cordier, S. (1995). The Role of Chemical, Physical, or Viral
Exposures and Health Factors in Neurocarcinogenesis: Implications for Epidemiologic
Studies of Brain Tumors.
Cancer Causes and Control, 6(3), 240-256.
Bookchin, D., & Schumaker, J. (1997). Tainted Polio Vaccine Still Carries Its Threat
40 Years Later.
The Boston Globe, January 26.
Carbone, M., et al. (1996). SV-40 Like Sequences in Human Bone Tumors.
Oncogene, 13(3), 527-535.
Elswood, B. F., & Stricker, R. B. (1995). Polio Vaccines and the Origin of AIDS.
Medical Hypotheses, 42(6), 347-354.
Fisher, B. L. (1997). Workshop on Simian Virus 40: A Possible Human Polyomavirus. National
Vaccine Information Center, January 27, On-line at
http://www.909shot.com/polio197.htm>http://www.909shot.com/polio197.htm.
Krieg, P., Amtmann E, Jonas, D., Fischer, H., Zang, K., & Sauer G. (1981). Episomal
Simian Virus 40 Genomes in Human Brain Tumors.
Proceedings of the National Academy of Sciences of the United States of America, 78(10),
6446-6450.
Lednicky, J. A., Garcea, R. L., Bergsagel, D. J., & Butel, J. S. (1995). Natural
Simian Virus 40 Strains are Present in Human choroid Plexus and Ependymoma tumors.
Virology, 212(2), 710-717.
Martini, F., et al. (1995). Human Brain Tumors and Simian Virus 40.
Journal of the National Cancer Institute, 87(17), 1331.
Martini, F., et al. (1996). SV-40 Early Region and Large T Antigen in Human Brain Tumors,
Peripheral Blood Cells, and Sperm Fluids From Healthy Individuals.
Cancer Research, 56(20), 4820-4825.
Pass, H. I., Kennedy, R. C., & Carbone, M. (1996). Evidence for and Implications of
SV-40 Like Sequences in Human Mesotheliomas.
Important Advances in Oncology, 89-108.
Rock, A. (1996). The Lethal Dangers of the Billion Dollar Vaccine Business.
Money, December, pages 148-163.
Tognon, M., et al. (1996). Large T Antigen Coding Sequences of Two DNA Tumor Viruses, BK
and SV-40, and Nonrandom Chromosome Changes in Two Glioblastoma Cell Lines.
Cancer Genetics and Cytogenics, 90(1), 17-23.
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