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"Swine Flu Shot May Rely on Emergency Use of Additives (Update1)


Last Edited: July 29, 2009, 2:13 pm

"Swine Flu Shot May Rely on Emergency Use of Additives (Update1)

By Tom Randall and Gary Matsumoto

"July 29 (Bloomberg) -- Swine flu vaccine makers may rely on a U.S. emergency declaration to use experimental additives made by GlaxoSmithKline Plc and Novartis AG to boost a limited supply of shots that will be available to fight the pandemic.

The ingredients, known as adjuvants, may be added for the first time to flu shots in the U.S. Health officials today are meeting to discuss the additives at the U.S. Centers for Disease Control and Prevention in Atlanta, and to recommend who should receive the limited amount of vaccines drugmakers say they will begin delivering in September or October.

The U.S. Health and Human Services Department declared a public health emergency over swine flu in April, and the Food and Drug Administration has the power to allow the use of unapproved medical products during such a crisis. The U.S. has been slow to approve the use of adjuvants because of safety concerns, and for fear of giving Americans an excuse to avoid getting the shots, said John Treanor, a University of Rochester researcher.

“The question is, do you really feel comfortable throwing this new thing into the mix and do you really need to?” said Treanor, a professor of medicine, microbiology and immunology at the school in Rochester, New York. “I myself, if I had to do it, would really wrestle with that decision.”

The CDC agreed to pay London-based Glaxo and Novartis, based in Basel, Switzerland, more than $415 million for adjuvants that could be added to the swine flu vaccines, according to a July 13 statement.

Early Production

Adjuvants may not be necessary if enough shots can be produced without them, according to Health and Human Services. That possibility got a boost today from authorities at the CDC, who said 40 million shots of unadjuvanted vaccine may be available in September, earlier than previously reported, with 80 million more doses ready in October.

A safety concern was raised in 2004 when researchers at the University of Florida in Gainesville reported that mice injected with oils used in the adjuvants developed conditions of the type that occur when the body’s immune system produces an excessive protective reaction. Similar reactions haven’t been seen in humans.

MF59, made by Novartis and sold in Europe, has been given to more than 40 million people, mostly adults, to prevent seasonal flu, according to the company. Glaxo’s adjuvant has proven safe and effective in clinical trials with 39,000 people, said Lisa Behrens, a spokeswoman for the company, in an e-mail. Glaxo will conduct more studies and continue to monitor safety after the vaccines are in use, she said.

Emergency Authorization

Under the U.S. health emergency, the FDA may authorize the use of unlicensed vaccines, according to Peper Long, an agency spokeswoman. The FDA convened an advisory committee July 23 to consider what trials are necessary for the vaccines’ approval. Advisory committees consist of medical experts who provide guidance to the agency.

Swine flu’s full force may reach the U.S. earlier than the typical flu season, according to the CDC. Vaccine makers are racing to make shots by mid-October, when cases are expected to rise in the northern hemisphere, fueled by cooler temperatures and the return of pupils to close quarters of classrooms.

The World Health Organization, based in Geneva, has said the H1N1 influenza, as the pandemic flu is known, is moving with “unprecedented speed.” The flu spread farther globally in less than six weeks than previous pandemics have in more than six months, the Geneva-based agency said on its Web site on July 17. Global health authorities have stopped counting the number of cases and the CDC says more than 1 million people Americans have been sickened by the virus.

Egg Yields

The vaccine makers have found it difficult to cultivate the quantities of virus needed for vaccine, as the strain yields 50 percent to 75 percent less antigen, the substance that induces immunity, compared with a typical seasonal flu strain, according to the WHO. The virus didn’t initially grow well in eggs, the principal medium used by the industry, vaccine makers said.

In the last week, scientists have been able to improve yields in eggs for the first time, which should ease pressure on manufacturers, Robin Robinson, chief of the Biomedical Advanced Research Development Authority, the U.S. agency in charge of buying the vaccine, said today. A decision on adjuvant use hasn’t been made, he said.

Mixing Oil, Water

The adjuvants are mixes of oil and water that -- by stimulating the immune system -- offer a way to boost the body’s response to antigen. Adjuvants, whose effectiveness vary by flu strain, may boost the strength of the antigen as much as 10- fold, as was the case with a bird flu vaccine approved in Europe, said Treanor, of the University of Rochester. By adding an adjuvant the same amount of antigen can be used to treat more people, he said.

“Until GlaxoSmithKline and Novartis can show me it won’t harm a rat or guinea pig, I think it’s a bad idea to give it to humans,” Vicky Debold, a registered nurse with a Ph.D. in public health, who is a member of the FDA’s advisory committee for reviewing vaccines, said July 27 in an interview.

The U.S. never had to consider the risks of an adjuvant because regular flu vaccines were deemed to have “worked so tremendously well,” said Lone Simonsen, research director in the department of global health at George Washington University in Washington.

“We have had a safe experience with the MF59-adjuvanted vaccine in Italy and Spain for many years now,” Simonsen said. “That experience we can lean on. That’s going to be the best data we have in time for using adjuvanted vaccines.”

U.S. Contracts

CSL Ltd., which has a $180 million order to supply bulk H1N1 antigen to the U.S. government, decided against boosting its vaccine with an adjuvant, preferring to use a formulation more closely resembling the seasonal flu shot, said Mary Sontrop general manager of the Melbourne-based company’s biotherapies unit.

The U.S. has contracts with five companies to provide flu shots. Novartis, based in Basel, Switzerland, is responsible for 45 percent of the supply, while Sanofi will provide 26 percent and CSL will make 19 percent, said Anthony Fauci, director of the National Institute of Allergy and Infectious Diseases in Bethesda, Maryland, in an interview last week.

The remaining doses will be made by Glaxo and London-based drugmaker AstraZeneca Plc."

Last Updated: July 29, 2009 13:25 EDT


Entry #1,284


time*treatComment by time*treat - July 29, 2009, 6:00 pm
The shots are so *safe*, they have given blanket "Immunity from Tort Liability" protection to everyone from the vaccine makers to the nurse who puts the needle into the victim's ... er ... patient's arm.
Rick GComment by Rick G - July 29, 2009, 6:39 pm
The liability immunity raises red flags a mile high. Why was that law passed in the first place? Because they knew back then that this man-engineered bio-weapon was going to be unleashed on us and they were going to create a "cure".   The criminality is appalling.

With today's sophistication in nanotechnology and genetic engineering, one would be foolish to allow them to put something into your body. They have demonstrated very clearly they are not to be trusted in any matter.
konaneComment by konane - July 29, 2009, 8:01 pm
Thanks Time*treat!! Yes and today on the news they're saying baby boomers show greater immunity due to flu going around in 1957 and Hong Kong flu in 1969. Some things about aging are good, this being one of them. OR maybe they're counting on baby boomers croaking from secondary infections thereby lessening future expenditures for that age group. A friend of mine jokingly says "perfect paranoia is perfect awareness ... or are they joking?
konaneComment by konane - July 29, 2009, 8:19 pm
Thanks Rick!!! This puzzles me ..... "The virus didn’t initially grow well in eggs, the principal medium used by the industry, vaccine makers said."              Wonder why??????????

I've used squaline both animal and plant origin for dry skin, but have never read of it being advised to take orally.

Now why are they adding it to an injectable that hasn't gone through extensive clinical testing as other vaccines have before being released for use on the general public?

All this coincides with railroading through health care mandates 80% of US citizens oppose out of common sense.
emilygComment by emilyg - July 29, 2009, 11:06 pm
konane - i've used it for dry winter skin, too. never thought of taking it internally.
konaneComment by konane - July 30, 2009, 12:17 am
Thanks Em!! Fractionated coconut oil is also excellent for winter skin. They use it in cosmetics, so you know it's thin and penetrating, also doesn't leave you feeling gooey or greasy.

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