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The influenza A (H5N1) vaccine (clade 2) is an inactivated, split-virion vaccine developed by Sanofi Pasteur for active immunization against H5N1 avian influenza. Specifically designed to target clade 2 H5N1 strains, including variants from Indonesia (clade 2.1) and China (clades 2.2 and 2.3), the vaccine induces neutralizing antibodies against the viral hemagglutinin (HA) protein. This mechanism blocks the virus from entering human cells, providing protection against infection. Developed between 2006 and 2008 as part of the U.S. government's pandemic preparedness strategy, the vaccine was manufactured at Sanofi's Swiftwater facility and supplied to the Strategic National Stockpile. It is administered via intramuscular injection and was not intended for commercial retail sale.
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