The Answer : Why vaccine makers need immunity from probes.

[Guest guest]

Zeus <info wrote: " Zeus " <info

" Zeus Subscribers " <info

A Glimpse into the Scary World of Vaccine Adjuvants

Sat, 19 Nov 2005 21:43:51 -0000

 

 

 

A Glimpse into the Scary World of Vaccine Adjuvants

 

By Edda West - Published in VRAN Newsletter - Winter 2005

Info www.vran.org

 

Adjuvants are formulated compounds, which when combined with vaccine antigens

intensify the body's immune response. They are used to elicit an early, high

and long-lasting immune response. " The chemical nature of adjuvants, their mode

of action and their reactions (side effect) are highly variable in terms of how

they affect the immune system and how serious their adverse effects are due to

the resultant hyperactivation of the immune system. While adjuvants enable the

use of less *antigen to achieve the desired immune response and reduce vaccine

production costs, with few exceptions, adjuvants are foreign to the body and

cause adverse reactions " , writes Australian scientist Viera Scheibner Ph.D,

(1)

 

The most common adjuvant for human use is an aluminum salt called alum derived

from aluminum hydroxide, or aluminum phosphate. A quick read of the scientific

literature reveals that the neurotoxic effects of aluminum were recognized 100

years ago. Aluminum is a neurotoxicant and has been linked to Alzheimer's

disease and other neurological disorders. Prior to 1980, kidney patients

undergoing long term dialysis treatments often suffered dialysis encephalopathy

syndrome, the result of acute intoxication by the use of an aluminium-containing

dialysate. This is now avoided using modern techniques of water purification.

In pre-term infants, prolonged intravenous feeding with solutions containing

aluminum is associated with impaired neurologic development. Scientists

speculate that aluminum neurotoxicity may be related to cell damage via free

radical production, impairment of glucose metabolism, and effects on nerve

signal transduction.(2) Vaccines which contain both aluminum adjuvants

and mercury based preservative, greatly magnify the neurotoxic effects. (3)

 

Macrophagic myofasciitis (MMF) is a muscle disease first identified in

1993, and has been linked to vaccines containing aluminum adjuvants.

Muscle pain is the most frequent symptom which can be localized to the

limbs or be more diffuse. Other symptoms include joint pain, muscle

weakness, fatigue, fever, and muscle tenderness. The disorder is associated with

an altered immune system in some, but not all patients. A study published in the

journal Brain (2001) revealed that 50 out of 50 patients had received vaccines

against hepatitis B virus (86%), hepatitis A virus (19%) or tetanus toxoid

(58%), 3-96 months (median 36 months) before biopsy. " We conclude that the MMF

lesion is secondary to intramuscular injection of aluminium hydroxide-containing

vaccines, shows both long-term persistence of aluminium hydroxide and an ongoing

local immune reaction, and is detected in patients with systemic symptoms which

appeared subsequently to vaccination " , write the authors of the study. (4)

 

But aluminum's neurotoxicity is of less concern to the vaccine industry

than the fact that it elicits a lesser antibody response to the so called

purer recombinant or synthetic antigens used in modern day vaccines than in

older style live or killed whole organism vaccines. " This has created a major

need for improved and more powerful adjuvants for use in these vaccines. " (5)

 

For decades, vaccine developers have been tinkering with various substances to

trick the body into heightened immune responses. The most effective adjuvants

are formulated with oils but have long been considered too reactive for use in

humans. Immunologists have known for decades that a microscopic dose of even a

few molecules of adjuvant injected into the body can cause disturbances in the

immune system and have known since the1930's that oil based adjuvants are

particularly dangerous, which is why their use has been restricted to

experiments with animals.

 

The classic oil based adjuvant called Freund's Complete Adjuvant can cause

permanent organ damage and irreversible disease - specifically autoimmune

diseases. When scientists want to induce autoimmune disease in a lab animal,

they inject it with Freund's Complete Adjuvant, which causes great suffering and

is considered by some too inhumane to even inject into animals.

 

Dr. Jules Freund creator of this oil based adjuvant warned in 1956 that

animals injected with his formulation developed terrible, incurable

conditions: allergic aspermatogenesis (stoppage of sperm production),

experimental allergic encephalomyelitis (the animal version of MS),

allergic neuritis (inflammation of the nerves that can lead to paralysis)

and other severe autoimmune disorders. (6)

 

Adjuvants can break " tolerance " , meaning they can disable the immune system to

the degree that it loses its ability to distinguish what is " self " from what is

foreign. Normally, the immune system ignores the constituents of one's own

body. Immunologists call this " tolerance " . But if something happens to break

" tolerance " , then the immune system turns relentlessly self-destructive,

attacking the body it is supposed to defend. (6)

 

Scientists theorize that oil based adjuvants have the ability to

" hyperactivate " the immune system, and in doing so, create chaos by

inducing such an extremely powerful response that the immune system

literally goes haywire and starts attacking elements it would normally

ignore. (6)

 

Another theory has to do with " specificity " . One of the great

distinguishing characteristics of the immune system is something akin to a

highly sensitive innate intelligence that has evolved over eons to be able

to respond very precisely to what it deems to be a threat to the body.

Because the body contains many types of oily molecules and lipids, it may be

that when an oil is injected, the immune system responds to it not only

specifically, but with heightened intensity because the oil adjuvant resembles

so closely the natural oils found in the body. A " cross reaction " then happens,

sending the immune system into chaos destroying any oils found anywhere in the

body that resemble the adjuvant oil. Demyelinating diseases like multiple

sclerosis are an example of this destructive autoimmune process. (6)

 

To deepen one's understanding of the shadowy world of vaccine development, award

winning investigative journalist Gary Matsumoto's new book is a " must read. " It

documents the secret human medical experimentation conducted on American

citizens by doctors and scientists working for the U.S. military. It is a book

about " betrayal of the most fundamental rules of medical ethics; and betrayal of

the basic duty of military and civilian leaders to protect the people they

govern. " Vaccine A: The Covert Government Experiment That's Killing our

Soldiers and Why GI's are Only the First Victims, is a gripping read into the

mad science world of the U.S. military's biowarfare vaccine development program

which, since 1987 has injected tens of thousands of U.S. troops with an

experimental unlicensed anthrax vaccine containing squalene. An oil based

adjuvant, squalene has

been known for decades to cause severe autoimmune diseases in laboratory

animals. Writes Matsumoto, " The unethical experiments detailed in this book are

ongoing, with little prospect of being self-limiting because they have been

shielded from scrutiny and public accountability by national security concerns. "

Reading this book, one gets a permanent chill in the spine as we glimpse the

" writing on the wall " of what is to come. (6,7)

 

" When UCLA Medical School's Michael Whitehouse and Frances Beck injected

squalene combined with other materials into rats and guinea pigs back in the

1970's, few oils were more effective at causing the animal versions of arthritis

and multiple sclerosis " , writes Matsumoto. In 1999, Dr. Johnny Lorentzen, an

immunologist at Sweden's Karolinska Institute proved that on injection,

" otherwise benign molecules like squalene can stimulate a self-destructive

immune response " , even though they occur naturally in the body. Other research

institutes have also shown that the immune system makes antibodies to squalene,

but only after it is injected (6) We now know that squalene, added to boost

immune response in a formulation known as MF59, is the secret ingredient in

certain lots of experimental anthrax vaccine that has caused devastating

autoimmune diseases and death

in countless Gulf War vets (Canadian, British and Australian troops were also

injected with squalene laced vaccine), and continues to be used today. There is

a " close match between the squalene-induced diseases in animals and those

observed in humans injected with this oil: rheumatoid arthritis, multiple

sclerosis and systemic lupus erythematosus " , writes Matsumoto. These three

illnesses have been proven to be caused by this oil, but there is an additional

long list of autoimmune diseases associated with squalene injection into

humans. (6) " There are now data in more than two dozen peer-reviewed

scientific papers, from ten different laboratories in the U.S., Europe, Asia and

Australia, documenting that squalene-based adjuvants can induce autoimmune

diseases in animals..observed in mice, rats, guinea pigs and rabbits. Sweden's

Karolinska Institute has demonstrated that squalene alone can induce the animal

version of rheumatoid arthritis. The Polish Academy of Sciences has shown

that in animals, squalene alone can produce catastrophic injury to the nervous

system and the brain. The University of Florida Medical School has shown that

in animals, squalene alone can induce production of antibodies specifically

associated with systemic lupus erythematosus " , writes Matsumoto. (6)

 

Long List of Side Effects Referring to squalene in her extensive article on

adjuvants, Dr. Scheibnerwrites, " This adjuvant contributed to the cascade of

reactions called " Gulf War syndrome " , documented in the soldiers involved in the

Gulf War. The symptoms they developed included arthritis, fibromyalgia,

lymphadenopathy, rashes, photosensitive rashes, malar rashes, chronic fatigue,

chronic

headaches, abnormal body hair loss, non-healing skin lesions, aphthous

ulcers, dizziness, weakness, memory loss, seizures, mood changes,

neuropsychiatric problems, anti-thyroid effects, anaemia, elevated ESR

(erythrocyte sedimentation rate), systemic lupus erythematosus, multiple

sclerosis, ALS (amyotrophic lateral sclerosis) also known as Lou Gehrig's

disease, Raynaud's phenomenon, Sjorgren's syndrome, chronic diarrhoea, night

sweats and low-grade fevers. (1)

Matsumoto punctuates his book with poignant interviews of military

personnel who suffered many of these extreme and devastating syndromes, all of

whom tested positive for anti-squalene antibodies which has become THE

definitive marker for people who have been injected with this adjuvant and who

have gone on to develop catastrophic diseases.

 

Immunologist, Dr. Pamela Asa was the first person to recognize that the

autoimmune diseases she was seeing in military personnel mirrored those in

experimental animals injected with oil formulated adjuvants. When she met a

patient with similar autoimmune symptoms who had participated in an experimental

herpes vaccine trial, who also knew he had been injected with MF59, a squalene

adjuvant being used as a 'placebo' in that study, everything began to fall into

place. Pam Asa contacted Dr. Robert Garry, a leading virologist at Tulane

University Medical School, whose specialty is developing antibody tests and

asked him to develop a test for the detection of anti-squalene antibodies - a

test that ultimately became the most important forensic and diagnostic tool

identifying patients whose autoimmune diseases followed injection with squalene

laced anthrax vaccine.(6) Juxtaposed to heart wrenching testimonies of shattered

health and ruined lives is the military's defiant stonewall and denial that a

squalene laced anthrax vaccine was injected into thousands

of its people without their informed consent - this despite the fact that the

FDA and independent researchers have tested and identified varying amounts of

squalene in specific lots of the vaccine.

 

Even more stunning is the fact that by 1997, hundreds of millions of

dollars had already been spent testing vaccines formulated with squalene

adjuvants by leading research institutes like NIH (National Institutes of

Health) who tested its efficacy in HIV vaccines, the National Cancer

Institute who for nearly two decades conducted research with

squalene-boosted vaccines, and the National Institutes of Allergy and

Infectious Diseases (NIAID) had been testing it in animals since 1988 and began

human clinical trials in1991. Nineteen of NIAID's 23 trials were for prototype

HIV vaccines.

 

Writes Matsumoto, " Squalene adjuvants are a key ingredient in a whole new

generation of vaccines intended for mass immunization around the globe. " (6)

Immune System Sees Squalene as an Enemy to Attack

Researchers at Tulane Medical School and the Walter Reed Army Institute of

Research " have both proven that the immune system responds specifically to the

squalene molecule. Squalene's pathway through the body has been tracked with a

radioactive tracer in animals by none other than Chiron, (well known flu vaccine

manufacturer) and maker of MF59, the squalene-based adjuvant, now also a

component of FLUAD, an Italian influenza vaccine. (6)

 

The immune system does in fact " see " squalene and recognizes it as an oil

molecule native to the body. The key is " route of administration " . As Gary

Matsumoto says, " Squalene is not just a molecule found in a knee or elbow - it

is found throughout the nervous system and the brain. " When it is injected into

the body, the immune system sees it as an enemy to be attacked and

eliminated.(6)

 

As any immunologist will tell you, the way an antigen encounters the immune

system makes all the difference. You can eat squalene - no problem as it is an

oil the body can easily digest.* But studies in animals and humans show that

injecting squalene will " galvanize the immune system into attacking it, which

can produce a self-destructive cross reaction against the same molecule in the

places where it occurs naturally in the body - and where it is critical to the

health of the nervous system. " (6) (injections are an unnatural route into the

body. A poison or toxic substance has the chance to be eradicated more easily

by any other means than by injection, which enters the blood, the deepest level

of the immune system)...Zeus

 

This phenomenon is also known as 'molecular mimicry', where the immune system

forms antibodies against one of its own structures and will continue to attack

the 'self' molecule in the body that resembles the one in the germ, or as is

the case with squalene, an identical substance that is naturally present in the

body. Once this self-destructive process begins, it never stops as the body

continues to make the molecule the immune system is now trained to attack.

 

Another example involving autoimmune 'molecular mimicry' is when the immune

system has been sensitized to attack myelin, the insulating fatty coating around

nerve fibres which ensures the smooth relay of nerve signals. The body would

continue to make myelin in order to replenish and repair the protective sheath

around its nerve endings. But says Matsumoto, " In the act of doing so, the body

immunizes itself against itself, administering over and over again what amounts

to a booster dose of something that the immune system now wants to get rid of.

This vital constituent (myelin) is now the enemy, and the immune system is now

programmed to obliterate it in an endless loop of self-destruction " - the

process involved in MS (multiple sclerosis), and ALS (Lou Gehrig's disease).(6)

 

Tying molecular mimicry to the autism epidemic, many children have

regressed into autism spectrum disorders after injection with the triple

live virus MMR (measles,mumps,rubella) vaccine. Dr.Vijendra Singh's

research at Utah State University suggests that auto-antibodies are

attacking myelin in these children. He has shown that many autistic

children have auto-antibodies to brain myelin basic protein (MBP) as well as

elevated levels of measles virus antibodies. " Immunoblotting analysis showed the

presence of an unusual MMR antibody in 60% (75 of 125) of autistic children, but

none of the 92 normal children had this antibody. In addition, there was a

positive correlation (greater than 90%) between MMR antibody and MBP

auto-antibody, suggesting a causal association between MMR and brain

autoimmunity in autism. This is one of the most important findings in autism to

date, which prompted us to link measles virus in the etiology of the disorder " ,

writes Dr. Singh. (8,9,10)

 

Immunologist Dr. Bonnie Dunbar has also done extensive research on the

mechanisms of injury inflicted by hepatitis B vaccine and has observed similar

autoimmune processes involving molecular mimicry in people who developed

devastating neuroimmune syndromes after injection with this vaccine. (11)

 

Molecular Mimicry as a Bio-Weapon

Matsumoto reports that Soviet bioweaponeers used the principal of molecular

mimicry in the 1980's to engineer a 'designer disease' that would attack myelin.

By splicing a fragment of myelin basic protein into legionella bacterium, they

created what amounted to a living " nano-bomb " , which they injected into guinea

pigs. What they found was that the immune system quickly cleared the legionella

bacterium, but the myelin molecule, smuggled in by this microbial " Trojan horse "

initiated a second wave of disease which caused experimental allergic

encephalomyelitis, the animal version of MS. The Soviets recognized this

creation for what it was - a biological time bomb!! (6)

 

" Squalene is a kind of trigger for the real biological weapon: the immune

system. When the immune system's full repertoire of cells and antibodies start

attacking the tissues they are supposed to protect, the results can be

catastrophic, " writes Matsumoto. His assessment is seconded by Dr. Pam Asa -

" Oil adjuvants are the most insidious chemical weapon ever devised. "

(6)

 

" Molecular mimicry, seen for its diabolical potential as a weapon by the

Soviets as far back as the 1980's, also applies to squalene. But the real

problem with using squalene, of course, is not that it mimics a molecule

found in the body; it is the same molecule, " writes Matsumoto. " So what

American scientists conceived as a vaccine booster was another " nano-bomb " ,

instigating chronic, unpredictable and debilitating disease. When the NIH

(National Institutes of Health) argued that squalene would be safe because it is

native to the body, just the opposite was true. Squalene's natural presence in

the body made it one of the most dangerous molecules ever injected into man! "

(6)

 

The main proponents for the use of squalene in vaccines have been the U.S

Department of Defense and the NIH. The anti-squalene antibodies in sick American

and British military personnel are evidence that military

experimentation has caused an unprecedented health catastrophe in tens of

thousands of people onto whom the vaccine was forced and who were denied the

right to make an informed decision based on existing scientific knowledge of the

dangers of injecting squalene. " By adding squalene to their new anthrax

vaccine, they did not make a better vaccine, they made a biological weapon. " (6)

..

Why, one would obviously ask, would anyone knowingly inject such a

dangerous substance into humans? Certainly in terms of the U.S. military's

decision, they chose to turn a blind eye to the existing science, which for

decades had documented the immune destructive properties of squalene. They

justified its use because they knew they had a weak and ineffective vaccine

which needed a serious boost. In the face of weaponized biowarfare agents like

anthrax already developed by Russia and fear that it was also possessed by Iraq,

they were desperate to increase the vaccine's effectiveness as they launched

into the first Gulf War. Additionally, explains Matsumoto, " scientists in the

United States are now literally invested in squalene. Army scientists who

developed the second generation anthrax vaccine have reputations to protect and

licensing fees to reap for the army..[and] .worldwide rights to develop and

commercialize the new recombinant vaccine for anthrax. " (6)

 

He goes on to explain, " the National Institutes of Health (NIH) has been

supporting both animal and human research with squalene since the 1980's.

Squalene has become perhaps the most ubiquitous oil adjuvant on the planet,

which is something that should concern everyone. Many of the cutting edge

vaccines currently in development by the NIH and its corporate partners contain

squalene in one formulation or another. There is squalene in the prototype

recombinant vaccines for HIV, malaria, herpes, influenza, cytomegalovirus and

human papillomavirus. Some of these prototypes like HIV, malaria and influenza

are intended for mass immunization around the globe. " (6)

 

Squalene Adjuvants Enter the Global Market

FLUAD, the squalene boosted flu vaccine has been licensed in Italy since 1997.

It contains MF59, the squalene adjuvant made by Chiron. Although all the

published papers co-authored by Chiron-employed scientists and Italian

researchers have reported MF59 to be safe, Gary Matsumoto suggests a flaw in

study designs may " prevent researchers from seeing the vaccine's real risks. "

Testing of FLUAD was limited to elderly people in nursing homes - average age

was 71.5 which would tend to obscure autoimmune problems that might arise for a

number of reasons. If autoimmune symptoms like joint pain and fatigue did occur

in geriatric Italians, doctors might not connect these complaints to anything

but old age. (6)

 

" Autoimmunity is notorious for taking years to diagnose because the early

symptoms (e.g. headaches, joint and muscle pain and fatigue) are so vague;

primary care physicians often fail to recognize it...a large Phase lV trial did

not even bother to analyze the " common-post immunization reactions " in study

participants, recording only those adverse events severe enough to require a

doctor's visit within 7 days of immunization. " In another study patients were

observed for 180 days, but only serious events like " admission to hospital or

death " qualified as a reaction - nothing else was recorded. Symptoms of adverse

reactions listed in the FLUAD package insert are almost identical to the Air

Force case-definition for Gulf War Syndrome, and include rashes, malaise, fever,

myalgia, arthralgia, weakness, sweating and various autoimmune reactions and

neurologic disturbances. (6)

 

" The question is whether scientists working for pharmaceutical companies are

intentionally designing studies so as to miss adverse reactions that

inconvenience their marketing strategy? " asks Matsumoto. " Chiron's conclusion

about squalene's safety are at odds with recent data from studies in both

animals and humans. " (6)

 

Just in from the newslists on February 9, 2005 is an item informing of the

European " debut " of a new adjuvant approved for use in a new high-potency

hepatitis B vaccine. Fendrix, the new enhanced hepB vaccine is being launched

by pharma giant GlaxoSmithKline for use in people with poor immune responses

(like dialysis patients) and those at high risk for developing hepatitis B. It

is formulated with a new adjuvant that can " significantly improve the

effectiveness of immunizations. " AS04, the 'proprietary' adjuvant based on MPL,

originally developed by U.S. company Corixa, " increases the immune potency of

the new vaccine, allowing two dose administration rather than three. It has

been shown clinically to be more effective than alum, the most widely used

adjuvant in vaccines. " (12)

 

So what exactly is this new high potency adjuvant? We're told by the press

release that MPL (AS04), is a " derivative of the lipid A molecule found in

Gram-negative bacteria, is extracted from bacterial cell walls (of what?) and is

one of the most potent regulators of the immune response, used by the body to

alert itself to bacterial infections. " (12) Full name of the lipid is

monophosphoryl lipid A (MPL)

 

This news should put everyone on high alert because guess what? Lipids are

oils/fatty acids and according to Matsumoto, MPL is identified in declassified

documents as one of two squalene emulsions used in the Army's new " recombinant

protective antigen anthrax vaccine (rPA) which the FDA, the National Institutes

of Health (NIH) and the Department of Defense fast-tracked into clinical trials

in1998. The other squalene adjuvant they used was Chiron's MF59. (6)

 

It appears that Fendrix is only the first of a whole new generation of

" enhanced potency " vaccines coming down the pipeline using the new high potency

lipid adjuvant, MPL. " The adjuvant is also being used in a number of GSK's

developmental vaccines, including one that could be the first effective vaccine

for malaria " , says the article. MPL (AS04) adjuvant is also a component of GSK

Bio's genital herpes vaccine, as well as a component in their cervical cancer

vaccine and a new tuberculosis vaccine. "

(12)

 

In the unraveling of the squalene story, we find that a squalene emulsion

first known as Triple Mix (based on Freund's adjuvant) was later given the

commercial name " Ribi " . Triple Mix (renamed Ribi) was tested by Dutch

scientists on rabbits who found it caused " severe effects.the largest number and

most severe lesions when compared with the other adjuvants. " (6)

 

Then in June 1999, Ribi ImmunoChem its manufacturer was acquired by Corixa

Corporation for $56.3 million, who presumably also own the Ribi formulation.

Whether MPL(AS04) is a formula related to Ribi is undoubtedly " proprietary "

information, but from Matsumoto's reseasrch, we know they are all squalene

based. And it doesn't end there. MPL, Corixa's multi-million dollar baby, is

slated for inclusion not only in the " enhanced potency " vaccines already

mentioned, but will also be a strategic component of new allergy and autoimmune

vaccines in development. (13)

 

From their inception, mass vaccinations have acted as a biological weapon,

undermining health, manipulating and crippling the immune system, and

instigating cycles of new and debilitating diseases. Monopoly medicine's

solution? Inject us with more powerful, genetically engineered high potency

vaccines. Never mind they are seeding us with " nano-bombs " that will further

attack our already compromised immune systems.

 

The concept of stimulating a hyperactive immune response by using oil-based

adjuvants has clearly backfired since we now know that the stronger the

antigenic response, the more damaging the adjuvant itself is to the normal

functioning of the brain and nervous system. The precedent for mass medical

experimentation via an ever increasing recommended vaccine schedule has been

set. We can now predict the grim future of mankind: an epidemic of neurological

disorders and autoimmune diseases never before imagined.

 

 

Notes & Resources

Adjuvants listed by Scheibner: " Today the most common adjuvants for human use

are aluminum hydroxide, aluminum phosphate and calcium phosphate. However, there

are a number of other adjuvants based on oil emulsions, products from bacteria

(their synthetic derivatives as well as liposomes) or gram-negative bacteria,

endotoxins, cholesterol, fatty acids, aliphatic amines, paraffinic and vegetable

oils. Recently, monophosphoryl lipid A, ISCOMs with Quil-A, and Syntex adjuvant

formulations (SAFs) containing the threonyl derivative or muramyl dipeptide have

been under consideration for use in human vaccines

 

*Definition of Antigen (Scheibner): " Micro-organisms, either bacteria or

viruses, thought to be causing certain infectious diseases and which the

vaccine is supposed to prevent. These are whole-cell proteins or just the

broken-cell protein envelopes, and are called antigens "

 

1.Viera Scheibner, Ph.D, The Adverse Effects of Adjuvants in Vaccines, Nexus

Magazine Dec. 2000 vol.8, No.1

http://www.whale.to/vaccine/adjuvants.html

2. Aluminum Toxicity notes from Dr. Boyd Haley Toxic Test Foundation website:

http://www.altcorp.com/DentalInformation/aluminumvaccines.htm

3. Boyd E. Haley, Professor of Chemistry: Thimerosal Containing Vaccines and

Neurodevelopment Outcomes:

http://64.41.99.118/vran/vaccines/mercury/mer_haley.htm

4. Brain, Vol. 124, No. 9, 1821-1831, September 2001, 2001 Oxford

University Press http://brain.oupjournals.org/cgi/content/abstract/124/9/1821

5 Vaccine Adjuvants: current state and future trends, Volume 82: Issue

Immunology and Cell Biology

http://www.blackwellpublishing.com/abstract.asp?ref=0818-9641 & vid=82 & iid=5 & aid=5\

& s= & site=1

6.Gary Matsumoto, Vaccine A-The Covert Government Experiment That's Killing our

Soldiers and Why GI's are Only the First Victims

7.Gary Matsumoto Press Release and biography: www.vaccine-a.com

8 Vijendra K Singh, Ph.D, Abnormal Measles Serology and Autoimmunity in Autistic

Children - Journal of Allergy & Clinical Immunol, 109 (1): S232, January 2002

9. Vijendra Singh - lecture at ATEDM Conference:

http://iquebec.ifrance.com/autismemtl/2002/program_en.html

10. Institute of Medicine Meeting (IOM) on Vaccines and Autism, February 9, 2004

11. Bonnie Dunbar, Ph.D - articles and research proposal - VRAN website:

http://64.41.99.118/vran/vaccines/hepatitis/dunbar_research.htm

12. New adjuvant debuts in new hep B vaccine , February 9, 2005, In-Pharma

Technologist.com

http://www.in-pharmatechnologist.com/news/news-ng.asp?n=57959-new-adjuvant-debut\

s

13. Corixa weblink to MPL press release on allergy & autoimmune applications:

http://www.corixa.com/default.asp?pid=auto_capsule & id=22

 

-----------------------

Sheri Nakken, R.N., MA, Classical Homeopath

http://www.nccn.net/~wwithin/vaccine.htm

 

forwarded by

Zeus Information Service

Alternative Views on Health

www.zeusinfoservice.com

All information, data and material contained, presented or provided herein is

for general information purposes only and is not to be construed as reflecting

the knowledge or opinion of Zeus Information Service.

Subscribe Free/Un:

info

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Music Unlimited - Access over 1 million songs. Try it free.