Universal protection against influenza infection by a multidomain antibody to influenza hemagglutinin.
Nick Stub LaursenRobert H E FriesenXueyong ZhuMandy JongeneelenSven BloklandJan VermondAlida van EijgenChan TangHarry A van DiepenGalina ObmolovaMarijn van der Neut KolfschotenDavid ZuijdgeestRoel StraetemansRyan M B HoffmanTravis NieusmaJesper PallesenHannah L TurnerSteffen M BernardAndrew B WardJinquan LuoLeo L M PoonAnna P TretiakovaJames M WilsonMaria P LimberisRonald VogelsBoerries BrandenburgJoost A KolkmanIan A WilsonPublished in: Science (New York, N.Y.) (2018)
Broadly neutralizing antibodies against highly variable pathogens have stimulated the design of vaccines and therapeutics. We report the use of diverse camelid single-domain antibodies to influenza virus hemagglutinin to generate multidomain antibodies with impressive breadth and potency. Multidomain antibody MD3606 protects mice against influenza A and B infection when administered intravenously or expressed locally from a recombinant adeno-associated virus vector. Crystal and single-particle electron microscopy structures of these antibodies with hemagglutinins from influenza A and B viruses reveal binding to highly conserved epitopes. Collectively, our findings demonstrate that multidomain antibodies targeting multiple epitopes exhibit enhanced virus cross-reactivity and potency. In combination with adeno-associated virus-mediated gene delivery, they may provide an effective strategy to prevent infection with influenza virus and other highly variable pathogens.