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The hemagglutinin (HA) protein of the Influenza B virus, specifically from the Victoria lineage, is a surface glycoprotein critical for viral entry into host cells. It binds to sialic acid receptors on host cells and mediates membrane fusion. As a major antigenic protein, it is a primary target for neutralizing antibodies and vaccine design. Victoria and Yamagata lineages differ antigenically, necessitating inclusion of both in quadrivalent vaccines. Victoria-lineage viruses may show preference for MUC5AC-positive cells and induce stronger interferon signaling compared to Yamagata.
Vaccines: elicit neutralizing antibodies that block receptor binding or membrane fusion. Monoclonal antibodies: block receptor binding or membrane fusion.
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