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      Both Neutralizing and Non-neutralizing Human H7N9 Influenza Vaccine-induced Monoclonal Antibodies Confer Protection

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          SUMMARY

          Pathogenic H7N9 avian influenza viruses continue to represent a public health concern and several candidate vaccines are currently being developed. It is vital to assess if protective antibodies are induced following vaccination, and to characterize the diversity of epitopes targeted. Here we characterized the binding and functional properties of twelve H7-reactive human antibodies induced by a candidate A/Anhui/1/2013 (H7N9) vaccine. Both neutralizing and non-neutralizing antibodies protected mice in vivo during passive transfer challenge experiments. Mapping the H7 hemagglutinin antigenic sites by generating escape mutant variants against the neutralizing antibodies identified unique epitopes on the head and stalk domains. Further, the broadly cross-reactive non-neutralizing antibodies generated in this study were protective through Fc-mediated effector cell recruitment. These findings reveal important properties of vaccine-induced antibodies and provide a better understanding of the human monoclonal antibody response to influenza in the context of vaccines.

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          Author and article information

          Journal
          101302316
          33345
          Cell Host Microbe
          Cell Host Microbe
          Cell host & microbe
          1931-3128
          1934-6069
          27 May 2016
          8 June 2016
          08 June 2017
          : 19
          : 6
          : 800-813
          Affiliations
          [1 ]The Department of Medicine, Section of Rheumatology, The Knapp Center for Lupus and Immunology Research, The University of Chicago, Chicago, IL 60637, USA
          [2 ]Department of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA
          [3 ]Graduate School of Biomedical Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA
          [4 ]Department of Pathology, University of Massachusetts Medical School, Worcester, MA 01655, USA
          [5 ]Division of Infectious Diseases and Immunology, Department of Medicine, University of Massachusetts Medical School, Worcester, MA 01655, USA
          [6 ]Division of Infectious Disease, Department of Medicine, University of Rochester School of Medicine and Dentistry, Rochester, NY 14642, USA
          [7 ]Center for Vaccine Biology & Immunology, Department of Microbiology & Immunology, University of Rochester School of Medicine and Dentistry, Rochester, NY 14642, USA
          [8 ]Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Disease, National Institutes of Health, Bethesda, MD 20852, USA
          [9 ]Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA
          Author notes
          [* ]Co-corresponding authors: (P.C.W.) wilsonp@ 123456uchicago.edu (F.K.) florian.krammer@ 123456mssm.edu
          [†]

          Carole J. Henry Dunand and Paul E. Leon contributed equally to the manuscript.

          Article
          PMC4901526 PMC4901526 4901526 nihpa789757
          10.1016/j.chom.2016.05.014
          4901526
          27281570
          29afefd6-13c9-49b6-925a-dc59d76e8ad2
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