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The hemagglutinin protein from Influenza A virus subtype H3N2 is an essential trimeric surface glycoprotein responsible for both attaching the virus to sialic acid-containing receptors on host cells and mediating subsequent membrane fusion required for infection. Its structure includes highly variable regions that allow immune evasion through antigenic drift—a process central to ongoing challenges with vaccine efficacy against this rapidly evolving pathogen. As such, it remains a principal focus for surveillance efforts and immunization strategies worldwide.
Neutralization of viral attachment and entry, inhibition of membrane fusion
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