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    Adeno-associated virus-vectored influenza vaccine elicits neutralizing and Fcγ receptor-activating antibodies (2020)

    Art
    Zeitschriftenartikel / wissenschaftlicher Beitrag
    Autoren
    Demminger, Daniel E.
    Walz, Lisa
    Dietert, Kristina (WE 12)
    Hoffmann, Helen
    Planz, Oliver
    Gruber, Achim D. (WE 12)
    von Messling, Veronika
    Wolff, Thorsten
    Quelle
    EMBO molecular medicine
    Bandzählung: 12
    Heftzählung: 5
    Seiten: e10938
    ISSN: 1757-4676
    Sprache
    Englisch
    Verweise
    URL (Volltext): https://www.embopress.org/doi/epdf/10.15252/emmm.201910938
    DOI: 10.15252/emmm.201910938
    Pubmed: 32163240
    Kontakt
    Institut für Tierpathologie

    Robert-von-Ostertag-Str. 15
    14163 Berlin
    +49 30 838 62450
    pathologie@vetmed.fu-berlin.de

    Abstract / Zusammenfassung

    The current seasonal inactivated influenza vaccine protects only against a narrow range of virus strains as it triggers a dominant antibody response toward the hypervariable hemagglutinin (HA) head region. The discovery of rare broadly protective antibodies against conserved regions in influenza virus proteins has propelled research on distinct antigens and delivery methods to efficiently induce broad immunity toward drifted or shifted virus strains. Here, we report that adeno-associated virus (AAV) vectors expressing influenza virus HA or chimeric HA protected mice against homologous and heterologous virus challenges. Unexpectedly, immunization even with wild-type HA induced antibodies recognizing the HA-stalk and activating FcγR-dependent responses indicating that AAV-vectored expression balances HA head- and HA stalk-specific humoral responses. Immunization with AAV-HA partially protected also ferrets against a harsh virus challenge. Results from this study provide a rationale for further clinical development of AAV vectors as influenza vaccine platform, which could benefit from their approved use in human gene therapy.