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Hemagglutinin glycoprotein (HA) enables influenza virus entry by mediating both attachment to sialylated receptors on host cells via its globular head domain and subsequent pH-triggered membrane fusion through its stem region. Its high variability drives antigenic evolution while conserved domains offer targets for broad-spectrum vaccines. As such, it remains central to influenza pathogenesis, immunity, diagnostics, surveillance efforts—and ongoing therapeutic innovation.
Neutralizing antibodies block receptor binding or inhibit conformational changes required for fusion.
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