OT? Vaccines and Genetic changes in humans..

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[CIA-DRUGS] Vaccines and Genetic Changes in Humans

Date:

Sun, 4 Feb 2001 04:24:07 EST

http://www.trufax.org/vaccine/vaccgen.html

Vaccines and Production of Negative Genetic Changes in Humans

© 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 e 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. 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.

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.

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