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(c) 1996-1998
Leading Edge Research Group
Vaccination and Genetic Change: Mobility of Genetic Material Between Life
Forms:
One of the indications that vaccinations may in fact be changing the genetic
structure of humans became evident in September of 1971, when scientists at the
University of Geneva made the discovery that biological substances entering
directly into the bloodstream could become part of human genetic structure.
Originally, Japanese bacteriologists discovered that bacteria of one species
transferred their own specific antibiotic resistance to bacteria of an entirely
different species. Dr. Maurice Stroun and Dr. Philip Anker in the Department of
Plant Physiology at the University of Geneva, began to accumulate evidence that
the transfer of genetic information is not confined to bacteria, but can also
occur between bacteria and higher plants and animals. According to an article
in World Medicine on September 22, 1971, "Geneva scientists are
convinced that normal animal and plant cells shed DNA, and that this DNA is
taken up by other cells in the organism."
In one experiment, scientists in Geneva extracted the auricles of frog
hearts and dipped them for several hours in a suspension of bacteria.
Afterward, they found a high percentage of RNA-DNA hybridization between
bacterial DNA extracted from bacteria of the same species as that used in the
experiment and titrated DNA extracted from the auricles which had been dipped
in the bacterial suspension. Bacterial DNA had been absorbed by the animal
cells. This phenomenon has been dubbed transcession. There is evidence
that this kind of phenomenon is happening all the time within the human body.
It is conceivable, for example, that heart damage following rheumatic fever
could the the result of the immune system reacting to its own cells producing a
foreign RNA complex after absorption of foreign DNA.
In Science magazine, November 10, 1972, bacterial RNA was
demonstrated in frog brain cells after a bacterial peritoneal infection. In the
April 1973 issue of the Journal of Bacteriology, transcription of
spontaneously released bacterial DNA was found to be incorporated into cellular
nuclei of frog auricles. Studies by Phillipe Anker and Maurice Stroun have
indicated spontaneous release of DNA material from mammalian cells, spontaneous
transfer of DNA from bacteria to higher organisms, spontaneous transfer of DNA
between cells of higher organisms, release of RNA by mammalian cells, and
biological activity of released complexes containing RNA.
Malignant Cellular Transformations Caused By Foreign DNA:
There is evidence that freely circulating foreign DNA can cause malignancy.
In a 1977 issue of International Review of Cytology, Volume 51, Anker
and Stroun discuss the possible effects of foreign DNA causing malignant cell
transformations. When foreign DNA is transcribed into a cell of a different
organism, "this general biological event is related to the uptake by cells
of spontaneously released bacterial DNA, thus suggesting the existence of
circulating DNA. In view of the malignant transformations obtained with DNA,
the oncogenic (cancer-causing) role of circulating DNA is postulated."
The discovery in 1975 that viruses causing cancer in animals had a special
enzyme called reverse transcriptase makes the problem even more
interesting. These kind of viruses are called RNA viruses. When an RNA
virus has the reverse transcriptase enzyme within its structure, it allows the
virus to actually form strands of DNA which easily integrate with the DNA of
the host cell which it infects. Studies by Dr. Robert Simpson of Rutgers
University indicate that RNA viruses which do not cause cancer can also fom
DNA, even without the presence of reverse transcriptase. DNA formed in this way
from an RNA virus is called a provirus. It is known that some
non-cancerous viruses have a tendency to exist as proviruses for long
periods of time in cells without causing any apparent disease. In other words,
they remain latent. Some examples of common RNA viruses that do not
cause cancer, per se, but have the capacity to form proviruses are
influenza, measles, mumps and polio viruses. In the October 22, 1967 British
Medical Journal, it was brought out by German scientists that multiple
sclerosis seemed to be provoked by vaccinations against smallpox, typhoid,
tetanus, polio, tuberculosis and diptheria. Even earlier, in 1965, Zintchenko
reported 12 cases in which MS became evident after a course of antirabies
vaccinations. Remember that millions of people between 1950 and 1970 were
injected with polio vaccines containing simian virus 40 (SV-40) transferred
from contaminated monkey kidney cells used to culture the vaccine. It is
impossible to remove animal viruses from vaccine cultures. You are reminded
that SV-40, the 40th virus to be discovered in simian tissue, is a
cancer-causing virus.
Immunization programs against influenza, measles, mumps and polio are in
fact seeding humans with RNA and forming proviruses which become latent for long
periods in throughout the body, only to re-awaken later on. Post-polio syndrome
is a good example of this problem. Other examples may include the so-called mesenchymal
and collegen diseases, such as rheumatoid arthritis, multiple sclerosis and
lupus erythmatosis, where antibodies are formed by the immune system against
the person's own tissues - tissues which have been impregnated with foreign
genetic material. According to a special issue of Postgraduate Medicine
in May 1962, "although the body generally will not make antibodies against
its own tissues, it appears that slight modification of the antigenic character
of tissues may cause it to appear foreign to the immune system and thus a fair
target for antibody production." Two years later in 1964, studies were
conducted on the polyoma virus, a tumor-producing DNA virus. It was
discovered that the persistent genetic DNA material in the polyoma virus
brought about malignant transformations in hamster embryo cell cultures. This
was reported in the November 23, 1964 issue of the Journal of the American
Medical Association.
Even common non-tumor viruses, including those in smallpox vaccine and polio
virus 2, can act as carcinogens. It was reported in Science on December
15, 1961 that these common viruses acted as catalysts in producing cancer
when given to mice in combination with known organic carcinogens in amounts
too small to induce tumors themselves. This means that some vaccinations
will induce cancer, when combined with the growing problem of environmental
pollution from toxic by-products of agriculture (pesticides on and in food) and
industry. Of course, this information is hidden from the public, which is why
the FDA, EPA and the agricultural industries can get away with
"sanctioning" small amounts of pollutants in food, water and air. The
connection has not been made public, much to the joy of the chemical industry,
the National Cancer Institute and the growing cancer industry, which continues
to fraudulently solicit public donations to justify its own existence. As an
aside, it has alreadybeen admitted that polio vaccinations have caused 100% of
all polio in the United States since 1980 and the predominant cases of all
paralytic polio since 1972 (Science, April 4, 1977). It is suspected
that the Salk and Sabin vaccines, made of moneky tissue culture, have also been
responsible for the major increase in leukemia in the United States.
The use of viruses, bacteria and animal tissue cultures in mass immunization
campaigns, considering that this information has been known for 20 years,
constitutes an intentionally created hazard to humans. The global impact
on the wide range of genotypes relative to human beings is difficult to assess,
but the outcome is definitely negative, and permitting the seeding of latent
proviruses in humans, knowingly, can have no other rationale other than
future medical profiteering, and constitutes a criminal conspiracy of vast
proportions which is tatamount to a genocidal policy against the population,
further constituting crimes against humanity, which is internationally
punishable by death. But, of course, especially in the United States, this
fact is ignored and suppressed from public knowledge, despite a 1984 plea by
some U.S. physicians to the United Nations in a report. The fact that this goes
on with the full knowledge of the world medical community makes this an international
conspiracy where the population has no recourse, given that vaccinations
are becoming mandatory and a prerequisite for many social programs.
Persistence of long-term viruses and foreign proteins and their relationship
to chronic and degenerative disease was also pointed out by Dr. Robert Simpson
of Rutgers University in 1976, when he addressed science writers at an American
Cancer Society seminar, saying "these proviruses could be molecules in
search of a disease." Dr. Wendell Winters, a virologist at the University
of California noted, "immunizations may cause changes in slow viruses and
changes in the DNA mechanism." Although host cells containing latent viral
particles operate more or less normally, they begin to synthesize viral
proteins under the guidance of the viral DNA, eventually creating the
circumstances for various autoimmune diseases, including diseases of the
central nervous system, which unfortunately add to the growing load of aberrant
social behavior patterns.
ALL
INFORMATION, DATA, AND MATERIAL CONTAINED, PRESENTED, OR PROVIDED HERE IS FOR
GENERAL INFORMATION PURPOSES ONLY AND IS NOT TO BE CONSTRUED AS REFLECTING THE
KNOWLEDGE OR OPINIONS OF THE PUBLISHER, AND IS NOT TO BE CONSTRUED OR INTENDED
AS PROVIDING MEDICAL OR LEGAL ADVICE. THE DECISION WHETHER OR NOT TO
VACCINATE IS AN IMPORTANT AND COMPLEX ISSUE AND SHOULD BE MADE BY YOU, AND YOU
ALONE, IN CONSULTATION WITH YOUR HEALTH CARE PROVIDER.