Flu blueprints in public database

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    Flu blueprints in public database

    Feb 2007 - The genetic 
    blueprints of more than 2,000 human and avian influenza 
    viruses taken from samples around the world now are available 
    in a public database to scientists everywhere for use in 
    developing new vaccines and therapies. 
    The Influenza Genome Sequencing Project, began in 2004, is 
    funded by the National Institute of Allergy and Infectious 
    Diseases, NIAID, one of the National Institutes of Health. 
    "This information will help scientists understand how 
    influenza viruses evolve and spread," NIH Director Dr. Elias 
    Zerhouni said Wednesday, "and it will aid in the development 
    of new flu vaccines, therapies and diagnostics." 
    Dr. Elias Zerhouni is director of the National Institutes of 
    Health. 
    The project has been carried out at the Microbial Sequencing 
    Center, managed by The Institute for Genomic Research, TIGR, 
    of Rockville, Maryland. 
    The Center will sequence more flu strains and samples and make 
    all sequence data freely available to the scientific community 
    and the public through GenBank. 
    The Internet accessible database of genetic sequences is 
    maintained by the National Center for Biotechnology 
    Information at NIH's National Library of Medicine, another 
    major contributor to the project. 
    Collaborators on the project include the U.S. Centers for 
    Disease Control and Prevention; the World Organization for 
    Animal Health/Food and Agriculture Organization Reference 
    Laboratory for Newcastle Disease and Avian Influenza in 
    Padova, Italy; and Canterbury Health Laboratories in 
    Christchurch, New Zealand. 
    “Scientists around the world can use the sequence data to 
    compare different strains of the virus, identify the genetic 
    factors that determine their virulence, and look for new 
    therapeutic, vaccine and diagnostic targets,” says NIAID 
    Director Anthony Fauci, M.D. 
    The project is directed by David Spiro, Ph.D., and Claire 
    Fraser, Ph.D., at TIGR and Elodie Ghedin, Ph.D., at the 
    University of Pittsburgh School of Medicine. 
    Dr. Elodie Ghedin sits in front of the image of an influenza 
    genome. 
    While deciphering genetic code was once a lengthy and 
    laborious process, automated technology now allows for rapid, 
    large-scale genomic sequencing. 
    Recently, growing sequencing capacity has enabled the 
    production rate to increase to more than 200 viral genomes per 
    month. 
    Seasonal influenza is a major public health concern in the 
    United States, accounting for approximately 36,000 deaths and 
    200,000 hospitalizations each year. 
    Globally, influenza results in an estimated 250,000 to half a 
    million deaths annually. 
    Seasonal flu shots are updated every year to target the latest 
    strains in circulation. Developing such vaccines is 
    challenging, however, because the influenza virus is prone to 
    high mutation rates when it replicates, and these mutations 
    can alter the virus enough that vaccines against one strain 
    may not protect against another strain. 
    An even greater concern is the potential for an influenza 
    pandemic caused by the emergence of a new, highly lethal virus 
    strain that is easily transmitted from person to person. 
    Health experts worry that the H5N1 viral strain of avian 
    influenza that has caused ... human deaths in ... countries as 
    well as the deaths of hundreds of millions of poultry might 
    mutate into a virus that easily spreads from human to human. 
    At the same time, progress is being made in developing a 
    vaccine against the H5N1 virus. 
    Last week, the World Health Organization, WHO, said 16 
    manufacturers from 10 countries are developing prototype 
    pandemic influenza vaccines to immunize humans against H5N1 
    avian influenza virus. Five of them are also involved in the 
    development of vaccines against other avian viruses (H9N2, 
    H5N2, and H5N3). 
    At present, more then 40 clinical trials have been completed 
    or are ongoing. Most of them have focused on healthy adults. 
    Some companies, after completing safety analyses in adults, 
    have initiated clinical trials in the elderly and in children. 
    All vaccines were safe and well tolerated in all age groups 
    tested. 
    For the first time, results presented at a meeting February 16 
    at the WHO headquarters in Geneva have convincingly 
    demonstrated that vaccination with newly developed avian 
    influenza vaccines can bring about a potentially protective 
    immune response against strains of H5N1 virus found in a 
    variety of locations. 
    Some of the vaccines work with low doses of antigen, which 
    means that significantly more vaccine doses can be available 
    in case of a pandemic. 
    In spite of the encouraging progress, WHO stresses that the 
    world still lacks the manufacturing capacity to meet potential 
    global pandemic influenza vaccine demand. Current capacity is 
    estimated at less than 400 million doses per year of trivalent 
    seasonal influenza vaccine. 
    In response to this challenge, WHO launched in 2006 the Global 
    pandemic influenza action plan to increase vaccine supply, a 
    US$10 billion effort over 10 years. 
    One of its aims is to enable developing countries to establish 
    their own influenza vaccine production facilities through 
    transfer of technology, providing them with the most 
    sustainable and reliable response to the threat of pandemic 
    influenza. 
    WHO is currently working with several vaccine producers, 
    mainly in developing countries affected by H5N1, to facilitate 
    establishment of in-country influenza vaccine production. 
    
    
    
    
    
    
    
    







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