In mice immunized with rAd-SHA2(Opt)FCD40L, highly significant levels of nasal IgA and circulatory IgG1 and IgG2a Abs with titers greater than fourfold compared with rAd-SHA2(wt) were also generated.
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Targeting the HA2 subunit of influenza A virus hemagglutinin via CD40L provides universal protection against diverse subtypes.
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