Vaccines and Production of Negative Genetic Changes in Humans

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Vaccines and Production of

Negative Genetic Changes in Humans

from 2003

http://www.inpharm.com/External/InpH/1,2688,1-4-0-0-inp_intelligence_news-0-

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Novel flu vaccine shows promise in mice

[Published: 05 June 2003 Source: Anti-Infective Drug News]

A new prototype vaccine developed by researchers at the Wistar Institute

might be able to protect recipients not only against this year's strains

of the virus, but also against those yet to come, possibly eliminating

the need for an annual treatment. A report on the new findings appears in

the 2nd June issue of Vaccine (2003;21:2616-2626).

Current flu vaccines trigger an immune response to a pair of prominent

viral-coat proteins that mutate constantly, which is why last year's flu

vaccine is ineffective against this year's flu strains. The experimental

vaccine contains an engineered peptide that mimics a third, smaller

viral-coat protein, called M2, that remains largely constant from year to

year.

Mice vaccinated with the vaccine generated a strong antibody (Ab)

response against M2. In fact, the mice generated a more powerful Ab

response to the vaccine than to infections by the flu virus itself. The

experimental vaccine was administered twice intranasally to mice. After

vaccination, a steep rise in M2-specific Abs was seen in blood samples

from the mice, and the mice exhibited significant resistance to viral

replication in the respiratory tract.

The researchers are also looking into whether the M2 element of the virus

might begin to mutate in the presence of the anti-M2 Abs generated by the

new vaccine. Their concern is that the observed viral stability in the M2

region of the flu virus may simply be a reflection of the fact that the

immune system does not mount a vigorous response to it, so that

evolutionary pressure on that region of the virus is not great.

Source: Anti-Infective Drug News, copyright Espicom Business Intelligence

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 form 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 anti-rabies

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 already been 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 monkey 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.

1: J Child Neurol. 2002

Sep;17(9):700-2.