Scientists hail the prospect of a universal vaccine for flu
Researchers have developed an antibody that could treat all strains of influenza A
Jeremy Laurance is Health Editor of The Independent and the i and has covered the specialism for more than 20 years. He thinks the harm medicine does is under-appreciated, the harm it prevents over-rated, and that cycling works better than most drugs. He was named Specialist Journalist of the Year in the 2011 British Press Awards.
Friday 29 July 2011
Scientists have developed a "super antibody" against flu that could be used as a universal treatment and pave the way for the development of a universal vaccine against the disease that affects billions of people every year.
If successful, the treatment could save lives, reduce pressure on intensive-care units during flu epidemics and save millions of pounds of NHS money. It is the first time a single antibody has been found effective against all strains of influenza A, the most common type which is responsible for global pandemics.
Scientists at the UK's Medical Research Council (MRC) working with colleagues in Switzerland found the antibody, FI6, was effective at preventing and treating flu in mice and ferrets. Antonio Lanzavecchia, who led the study published in Science Express, said: "I would expect it to work very well in humans."
Other approaches to developing a universal vaccine that did not rely on antibodies were unlikely to work. "Antibodies are the key," he said.
Sir John Skehe,l of the MRC, said the antibody could also be used as a treatment in conjunction with Tamiflu, the drug that reduces the severity of flu. The treatment would be reserved for hospitalised patients but it might have the potential to save lives and reduce demand for intensive care.
He said: "The problem with Tamiflu is that you can get resistance. If you use them together [with the antibody] you could reduce resistance. Even though the 2009 flu pandemic was mild, intensive care units (ITU) across the UK were full. Caring for patients in ITU is hugely expensive – if you could reduce the pressure on intensive care that would be a real plus."
Sir John added that a single antibody provided a "clear advantage" in terms of developing a universal vaccine against influenza A because it was possible to identify the site on the virus where the antibody bonded.
Researchers at Oxford University announced earlier this year that they had tested a universal flu vaccine on human volunteers but that employed a different mechanism which involved increasing the body's T-cells to boost the immune response.
Last year, a privately owned drug discovery group, Seek, announced it was testing a universal flu vaccine also based on the T-cell response.
Steve Gamblin, from the National Institute for Medical Research, said of the latest study: "Historically, it has been impossible to predict precisely what kind of flu could develop into an epidemic and, as such, it has been necessary to develop new vaccines each year to tackle the different viruses. Our discovery may eventually help to develop a universal vaccine."
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