Scientists Learn How Adjuvant Makes Vaccines Effective
Main Category: Public HealthArticle Date: 18 Jun 2004 - 8:00 PDT
'Scientists Learn How Adjuvant Makes Vaccines Effective'
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Eighty years after adjuvants were first used to boost the effectiveness of vaccines, researchers at National Jewish Medical and Research Center have finally begun to understand how they work. They report in the June 18 issue of Science that the most common adjuvant, alum, provokes a previously unrecognized group of immune-system cells to secrete the protein interleukin-4, which primes B cells for a better response to the vaccine.
"Adjuvants have been included in vaccines given to hundreds of millions of people for decades," said Michael Jordan, M.D., co-lead author and researcher at National Jewish. "These findings give us new insight into how they boost the immune response to a vaccine."
Live vaccines, containing weakened forms of an infectious organism, generally work fine by themselves. But vaccines containing dead organisms (inactivated vaccines) or pieces of the infectious organisms or their toxins (acellular or recombinant vaccines) generally need adjuvants to boost their effectiveness. Aluminum salts, known as alum, are the only adjuvant approved for use in the United States for routine preventive vaccines.
The discovery of alum as a vaccine booster actually began with tapioca, a starchy substance used in pudding and as a thickener in cooking. In the early 1920s a scientist named Ramone reported that, for unknown reasons, he had mixed tapioca with inactivated tetanus toxin and found that it served as a more effective vaccine than did the toxin itself. Several years later, a researcher named A.T. Glenny read Ramone's account and decided to mix aluminum salts, or alum, with inactivated tetanus toxin in a test vaccine he tried on rabbits. Again the vaccine with the adjuvant was more effective than a vaccine containing the toxin alone.
The adjuvant alum was first widely used in humans in the 1950s as part of the Salk poliomyelitis vaccine. Since then, adjuvants have been widely used in many vaccines, including the Diptheria/Tetanus/Pertussis (DtaP), Hepatitis, Haemophilus influenzae (Hib), typhoid and some flu vaccines.
No one fully understands why adjuvants boost the effectiveness of nonliving vaccines. Several theories have been proposed but none have been widely accepted.
The National Jewish team was investigating a phenomenon known as MHC class II signaling, which occurs during interactions between B cells and T cells. When properly stimulated, B cells mature into plasma cells, which release antibodies, one of the immune system's major disease-fighting tools.
However, researchers had noticed that B cells must be prepared, or primed, if they are to be stimulated through this signaling pathway. If not primed, they will do nothing or even self-destruct. Priming, however, had been mainly observed in cell cultures. The National Jewish team wanted to determine whether priming occurs in animals, learn how it occurs, and how it might affect the overall antibody response.
They discovered that the injection of the adjuvant alum alone could prime B cells in mice. Then they discovered that cells bearing a marker known as Gr1 appeared in the spleen shortly after the injection of alum into mice. Gr1 is a marker found on a variety of immune-system cells, including granulocytes.
This group of Gr1 cells in the spleen had not been previously recognized, and researchers have not yet completely characterized them. But they did show that the Gr1 cells secrete interleukin-4 and that both the Gr1 cells and the interleukin-4 are necessary for the priming of the B cells. When they inactivated the Gr1 cells, mice responded to a vaccine containing the adjuvant with fewer B cells and fewer antibodies.
"Our research shows that alum injection triggers the accumulation of Gr1 cells in the spleen, which prime B cells and facilitate their response to vaccines," said senior author John Cambier, Ph.D., Chairman of the Integrated Department of Immunology at National Jewish and the University of Colorado Health Sciences Center. "We suspect that alum may influence the immune system in other ways as well. Our findings, however, have begun to unravel the mystery of adjuvants and will lead us in the future to better understand how they have helped prevent disease in millions of people. By understanding how they work we may be able to design new and more effective adjuvants".
Contact: William Allstetter
(303) 398-1002
allstetterw@njc.org
http://www.nationaljewish.org/news/alum.html
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26 May. 2012. <http://www.medicalnewstoday.com/releases/9615.php>
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Visitor Opinions (latest shown first)
Live vaccine preparation
posted by A. El-kholy on 21 Jul 2010 at 11:48 amI'm wondering if you can give me a good reason of not using adjuvants in preparation of live viral vaccines.I have prepared a gene deleted virus vaccine for cattle and I included an oil adjuvant in the vaccine formula. The seroconversion was really good and neutralizing antibody titers were protective as early as 2 weeks post-vaccination. Did I do wrong on scintific basis, taking into consideration that my constructed virus was a bit less cytotoxic in cell cultures than the putative virus strain.
I'll really appreciated it if you respond promptly.
Thanks
Dr Alaa
OIL And Water Won't Mix - ADJUVANT
posted by Christopher-Peter on 17 Sep 2009 at 1:00 pmOIL and Water Won't Mix - ADJUVANT
The Greatest Story Never Told - Chapter Three
For the past 17 years, the U.S. Army has been working on a new anthrax vaccine that contains no anthrax, and is made with an ingredient that it does not want to name. That ingredient is called squalene. Squalene is an oil. Without it, the new vaccine will not work any better that the old one. In fact, for all intents and purposes, without squalene the new vaccine is the old one. What makes squalene so important is it's proven ability to stimulate a strong response from the immune system.
Immunologist have a special name for substances used to boost feeble vaccines. They are called ADJUVANTS. Adjuvants are arguably the most extensively researched pharmaceutical product in the last quarter century that you NEVER HEARD OF.
I have used the word adjuvant three times in this paragraph so far and that is probably three times more than you have ever seen it in print. This is partly because the most effective adjuvants, those formulated with oils, ARE TOO DANGEROUS FOR HUMAN USE. That is squalene's other proven ability, causing incurable disease, which is why it is such a touchy subject with the Department of Defense.
Today, only one adjuvant - an aluminum salt called aluma - is licensed for human use. All the oil adjuvants are so noxious that their use are restricted to experiments with animals, and even then, governments have written strict regulations to govern how they are used.
The classic oil adjuvant, called Freund's Complete Adjuvant can cause permanent organ damage and incurable disease. As early as the 1930s, these oil additives were notorious for inducing illness. By the 1950s, scientist knew these illnesses were specifically AUTOIMMUNE. Today that is their chief use in research - inducing disease instead of preventing it. Scientist studying autoimmune disease cannot wait around for it's spontaneous appearance in a lab animal.
Autoimmune diseases are chronic and progressively debilitating ailments; some, like Multiple Sclerosis and Lupus, can be fatal. They occur when the immune system looses its ability to distinguish what is 'self'ť from what is foreign. Under normal circumstances, your immune system ignores the constituents of your own body; immunologist call this 'tolerance.'ť But, IF TOLERANCE IS BROKEN, the immune system turns relentlessly self-destructive, attacking the body it is suppose to defend.
Here is what they were not telling anyone. By 1964, the year when everyone in the military was supposed to get immunized with an OIL-BOOSTED INFLUENZA VACCINE, the Army already knew the risks this vaccine presented for a very specific type of illness. AFEB's Colonel Abram S. Benenson had drawn up a list of diseases that investigators should watch out for in veterans injected with the oily flu vaccine at Fort Dix. Benenson's list read like the contents of a chapter on autoimmune disease in an immunology text book. It included Multiple Sclerosis, Myelitis, Guillain-Barre syndrome (GBS), Uveitis, Neuro-Dermatitis Circumscripta and Disseminata, Amyloidosis, Lupus- Erythematousus, Dematomyositis, Scleroderma, Chronic Pericarditis, Raynaud's disease, Rheumatoid Arthritis, Rheumatoid Myositis and acute Glomerulonephritis - all of them AUTOIMMUNE DISEASES.
Epidemiologists, mainly working for the National Research Council And the American Cancer Society, reported a 'significant excess of deaths' in soldiers (TROOPS) given the OIL-BOOSTED VACCINE, which the investigators related to 'ill-defined vascular lesions of the central nervous system.'ť They attributed this fact to the greater number of autopsies performed on the soldiers given the oil-boosted vaccine.
ADJUVANTS can break TOLERANCE - read more from: Vaccine A: the covert government experiment that's killing our soldiers and Why GI's Are Only the First Victims - By Gary Matsumoto
A free preview of the complete, Chapter Three, is available on line - you must read this
http://books.google.com/books?id=Irw82Iv5nyoC&printsec=frontcover&source=gbs_navlinks_s#v=onepage&q=&f=false
CTV.ca News - September 1, 2009
H1N1 plan fails at-risk groups, journal warns.
The federal government is ill prepared to protect vulnerable populations in Canada, warns the Canadian Medical Association Journal (CMAJ).
The journal's editor, Dr. Paul Hebert says; the PUBLIC HEALTH AGENCY of CANADA (PHAC) plans to immunize the entire Canadian population.
But Herbert, and vaccine expert Dr. Noni MacDonald, write that the federal government needs to fast-track the vaccine for pregnant women, children and people with chronic diseases.
PHAC has opted to order a version of the vaccine containing ADJUVANT, a chemical additive that ramps up the response the immune system generates to the vaccine.
"An adjuvant allows you to take a full dose of the vaccine and divide it in four... and vaccinate four people," Hebert explained.
But that type of vaccine also takes longer to approve than vaccines without adjuvant because it needs to be reviewed more thoroughly.
http://www.ctv.ca/servlet/ArticleNews/story/CTV.../20090831?hub=Health
Information compiled and provided by Christopher-Peter: Maingot; without prejudice, malice aforethought, ill will, vexation, or frivolity.
ADJUVANT - VACCINE Booster Or "nano-bomb"???
posted by Christopher-Peter on 15 Sep 2009 at 4:43 pmThey were intent on creating something Mother Nature had not. 'Designer disease,' they would later call it.
Dr. Sergei Popov was one of the Soviet Union’s best germ warriors, and running highly classified field research projects at The State Research Center of Applied Microbiology at Obolensk, and another laboratory in Siberia, specializing in viruses called VECTOR. While at Obolensk, Popov supervised a program codenamed 'FACTOR' as in 'pathogenic factors' or 'virulence factors' where he helped engineer designer germs resistant to antibiotics. That is when he got interested in U.S. research with myelin basic protein.
American molecular biologist had mapped out the entire amino acid sequence for myelin - one of the chief components of the insulation surrounding nerve endings. Now they were hard at work trying to identify the epitopes on viruses that would cross-react with a special site on the myelin molecule to which an antibody might react and, cause experimental allergic encephalomyelitis - the animal version of multiple sclerosis. As the California-based scientists Robert Fujinami and Michael Oldstone explained in a landmark paper in Science: 'during the cross-reacting immune response, virus may be cleared, but the components of the immune attack continues to assault self elements. The autoimmune response leads to tissue injury that, in turn, releases more self antigen, and the cycle continues.'ť Fujinami and Oldstone called the initial infection a 'hit and run event.'ť By this they meant the virus attacked, and though it didn't stick around, it left behind lasting damage. That is because the immune system continues to attack the molecule in the body that resembles the one in the germ, long after the immune system has gotten rid of the germ. Once this self-destructive process begins, it never stops; our bodies continue making the molecule the immune system is now trained to attack. If this new target for the immune system happened to be myelin, for example, the body would continue making this protein in order to replenish and repair the sheath around it's nerve endings. But 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 of your own body is now the enemy, and the immune system is now programmed to obliterate it in an endless loop of self-destruction [italics mine]. Dr. Sergei Popov saw real potential here.
He would not bother looking for a naturally occurring molecule that could trigger this process. He would make one. Popov spliced a fragment of myelin basic protein into legionella - the bacterium that causes Legionnaire's Disease - creating a 'chimera,' named for the mythical creature with a lion's head, goat's body and serpent's tail. Inside Popov's new constructed chimera was what amounted to a living 'nano-bomb' molecular contraband that could theoretically cause MS. When Popov infected guinea pigs with his chimera, the immune system cleared the legionella, and, just as he predicted, the myelin molecule smuggled into the guinea pigs inside of his microbial Trojan horse germ initiated a second wave of disease. This stealth germ caused experimental allergic encephalomyelitis, the animal version of MS. Popov felt as proud as a new parent. He could not wait to show 'the client.'
'The client'ť is what VECTOR scientists called the Soviet Army officers who commissioned their biological warfare research projects. 'Their initial response was rather discouraging,' says Popov, 'because they did not see the fast onset of symptoms.'ť What the generals were accustomed to seeing was a germ with an immediate and catastrophic effect, but when they came back a few weeks later and saw the guinea pigs crippled MS, they recognized Popov's creation for what it was - a biological time bomb. Soviet scientists then constructed another one of these time bombs with a virus. They chose vaccinia, the non-lethal cousin of smallpox. Popov, who is now living in America, believes the 'final construct' for this viral time bomb was not vaccinia, but smallpox itself. In any case, it worked. 'The client'ť had seen enough. The generals were sold on the idea. 'The Russian Ministry of Defense wanted us to construct these designer germs, using myelin basic protein from monkeys and humans,' says Popov. 'That would create a human version of the disease.'
Molecular mimicry, seen for its diabolical potential as a weapon by the Soviets as far back as the 1980s, also applies to SQUALENE [caps mine]. 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. So what American scientists conceived as a vaccine booster was another 'nano-bomb,'ť instigating chronic, unpredictable and debilitating disease. When the National Institutes of Health (NIH), 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 injected into human beings. When UCLA Medical School's Michael Whitehouse and Frances Beck injected squalene combined with other materials into rats and guinea pigs back in the 1970s, few oils were more effective at causing the animal versions of ARTHRITIS, and MULTIPLE SCLEROSIS [caps mine]. By the late 1990s, Sweden's Karolinska Institute proved that injecting squalene all by itself could cause arthritis. The Polish Academy of Sciences proved that squalene alone could severe neurological damage. Now Tulane University Medical School and its ardent intellectual adversary 'the Army's Col. Carl Alving' have both shown that the immune system makes antibodies to squalene, but only after it is injected.
For Squalene's proponents in the U.S. Army and the NIH, this has been a relentless march towards an unpalatable truth. By adding squalene to their new anthrax vaccine, they did not make a better vaccine; they made a biological weapon [italics mine]. The anti-squalene antibodies in sick U.S. and British military personnel are evidence that military experiments may have caused more casualties with its new anthrax vaccine than have been caused by anthrax weapons since they were first used by the Japanese Army in the 1940s.
The above is an excerpt from Gary Matsumoto's book (with modifications):
VACCINE.A
The Covert Government Experiment
That's Killing Our Soldiers
and Why GI's Are Only the First Victims
books.google.com/books?id=Irw82Iv5nyoC&a...e&q=&f=false
CANADA'S VACCINE MAKER says single dose of ADJUVANTED VACCINE protective.
September 14, 2009 - THE CANADIAN PRESS
[caps mine]
TORONTO - A shot of swine flu vaccine that is about a third of the size of a standard dose is protective when BOOSTED WITH an additive called an ADJUVANT, CANADA'S PANDEMIC VACCINE MANUFACTURER (GlaxoSmithKline) said Monday.
A single shot containing 5.25 micrograms of VACCINE and the company's AS03 ADJUVANT had a SPIKE in ANTIBODY LEVELS thought to signal protection
[caps mine].
MP has H1N1 concerns.
CBC News - September 14, 2009
An NDP MP from Winnipeg: Judy Wasylycia-Leis wants to know what measures Elections Canada has in place to safeguard voters from the spread of swine flu, considering an election poses significant health risks with large public events and many people coming into contact during canvassing...hmmm
(hmmm-mine).
$400M contract goes to GlaxoSmithKline factory in Quebec City.
August 6, 2009 - CBC News.
Canada to order 50.4 million H1N1 (SWINE FLU) vaccine doses - One dose should be enough, because: GlaxoSmithKline is using an additive (AS03 - SQUALENE based) known as ADJUVANT. Adjuvants are used to boost immune response from vaccines [italics, caps and info on AS03 mine].
THE WORLD HEALTH ORGANIZATION (WHO) recommends countries should use SWINE FLU vaccines with ADJUVANTS [caps mine] - to stretch the global supply of the vaccines.
August 4, 2009 - THE CANADIAN PRESS
Flu vaccines in Europe often contain adjuvants [italics and underline mine].
The European Medicines Agency has previously said swine flu vaccines based on a pre-approved bird flu vaccine could be licensed within five days, even without extensive testing in humans.
In the United States, there are no licensed flu vaccines with adjuvants - The U.S. has ordered $979 million worth of bulk vaccine and Novartis' adjuvant (MF59®).
Boosting compounds called adjuvants complicate licensing of pandemic vaccines.
July 28, 2009 - THE CANADIAN PRESS
Neither country, CANADA and the UNITED SATES, has licensed flu vaccines with adjuvants in them before, making the addition of the oil-and-water emulsions a potential hurdle to fast-track pandemic vaccines.
MF59; is a sub-micron oil-in-water emulsion of a squalene, polyoxyethylene sorbitan monooleate (TweenTM 80) and sorbitan trioleate. SQUALENE is a natural organic compound originally obtained from shark liver oil and a biochemical precursor to steroids. The “MF59” adjuvant was developed by Chiron Corp., a company acquired by Novartis. MF59 is approved in Europe and is found in several vaccines; such as an influenza vaccine manufactured by Novartis. It has also been licensed to other companies and is being actively tested in vaccine trials [caps mine].
http://www.whale.to/vaccines/mf59_h.html
Information compiled and provided by Christopher-Peter: Maingot; without prejudice, malice aforethought, ill will, vexation, or frivolity.
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