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Alveolar macrophages are critical for broadly-reactive antibody-mediated protection against influenza A virus in mice

Author

Listed:
  • Wenqian He

    (Icahn School of Medicine at Mount Sinai
    Graduate School of Biomedical Sciences, Icahn School of Medicine at Mount Sinai)

  • Chi-Jene Chen

    (Icahn School of Medicine at Mount Sinai)

  • Caitlin E. Mullarkey

    (Icahn School of Medicine at Mount Sinai)

  • Jennifer R. Hamilton

    (Icahn School of Medicine at Mount Sinai
    Graduate School of Biomedical Sciences, Icahn School of Medicine at Mount Sinai)

  • Christine K. Wong

    (Icahn School of Medicine at Mount Sinai)

  • Paul E. Leon

    (Icahn School of Medicine at Mount Sinai
    Graduate School of Biomedical Sciences, Icahn School of Medicine at Mount Sinai)

  • Melissa B. Uccellini

    (Icahn School of Medicine at Mount Sinai)

  • Veronika Chromikova

    (Icahn School of Medicine at Mount Sinai)

  • Carole Henry

    (The University of Chicago)

  • Kevin W. Hoffman

    (Icahn School of Medicine at Mount Sinai)

  • Jean K. Lim

    (Icahn School of Medicine at Mount Sinai)

  • Patrick C. Wilson

    (The University of Chicago)

  • Matthew S. Miller

    (McMaster University)

  • Florian Krammer

    (Icahn School of Medicine at Mount Sinai)

  • Peter Palese

    (Icahn School of Medicine at Mount Sinai)

  • Gene S. Tan

    (Icahn School of Medicine at Mount Sinai
    J. Craig Venter Institute)

Abstract

The aim of candidate universal influenza vaccines is to provide broad protection against influenza A and B viruses. Studies have demonstrated that broadly reactive antibodies require Fc–Fc gamma receptor interactions for optimal protection; however, the innate effector cells responsible for mediating this protection remain largely unknown. Here, we examine the roles of alveolar macrophages, natural killer cells, and neutrophils in antibody-mediated protection. We demonstrate that alveolar macrophages play a dominant role in conferring protection provided by both broadly neutralizing and non-neutralizing antibodies in mice. Our data also reveal the potential mechanisms by which alveolar macrophages mediate protection in vivo, namely antibody-induced inflammation and antibody-dependent cellular phagocytosis. This study highlights the importance of innate effector cells in establishing a broad-spectrum antiviral state, as well as providing a better understanding of how multiple arms of the immune system cooperate to achieve an optimal antiviral response following influenza virus infection or immunization.

Suggested Citation

  • Wenqian He & Chi-Jene Chen & Caitlin E. Mullarkey & Jennifer R. Hamilton & Christine K. Wong & Paul E. Leon & Melissa B. Uccellini & Veronika Chromikova & Carole Henry & Kevin W. Hoffman & Jean K. Lim, 2017. "Alveolar macrophages are critical for broadly-reactive antibody-mediated protection against influenza A virus in mice," Nature Communications, Nature, vol. 8(1), pages 1-14, December.
  • Handle: RePEc:nat:natcom:v:8:y:2017:i:1:d:10.1038_s41467-017-00928-3
    DOI: 10.1038/s41467-017-00928-3
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