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Fcγ Receptor Function and the Design of Vaccination Strategies

Journal

IMMUNITY
Volume 47, Issue 2, Pages 224-233

Publisher

CELL PRESS
DOI: 10.1016/j.immuni.2017.07.009

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Funding

  1. Rockefeller University
  2. National Institute of Allergy and Infectious Diseases of the National Institutes of Health [P01AI100148, U19AI111825, U19AI109946]
  3. National Cancer Institute [R35CA196620, P01CA190174]
  4. Bill & Melinda Gates Foundation [OPP1124068]

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Through specific interactions with distinct types of Fc gamma receptors (Fc gamma Rs), the Fc domain of immunoglobulin G (IgG) mediates a wide spectrum of immunological functions that influence both innate and adaptive responses. Recent studies indicate that IgG Fc-Fc gamma R interactions are dynamically regulated during an immune response through the control of the Fc-associated glycan structure and Ig subclass composition on the one hand and selective Fc gamma R expression on immune cells on the other, which together determine the capacity of IgG to interact in a cell-type-specific manner with specific members of the Fc gamma R family. Here, we present a framework that synthesizes the current understanding of the contribution of Fc gamma R pathways to the induction and regulation of antibody and T cell responses. Within this context, we discuss vaccination strategies to elicit broad and potent immune responses based on the immunomodulatory properties of Fc-Fc gamma R interactions.

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