Development and Characterization of Monoclonal Antibodies Specific for Mouse and Human Fcγ Receptors

J Immunol. 2015 Dec 1;195(11):5503-16. doi: 10.4049/jimmunol.1402988. Epub 2015 Oct 28.

Abstract

FcγRs are key regulators of the immune response, capable of binding to the Fc portion of IgG Abs and manipulating the behavior of numerous cell types. Through a variety of receptors, isoforms, and cellular expression patterns, they are able to fine-tune and direct appropriate responses. Furthermore, they are key determinants of mAb immunotherapy, with mAb isotype and FcγR interaction governing therapeutic efficacy. Critical to understanding the biology of this complex family of receptors are reagents that are robust and highly specific for each receptor. In this study, we describe the development and characterization of mAb panels specific for both mouse and human FcγR for use in flow cytometry, immunofluorescence, and immunocytochemistry. We highlight key differences in expression between the two species and also patterns of expression that will likely impact on immunotherapeutic efficacy and translation of therapeutic agents from mouse to clinic.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibodies, Monoclonal / immunology*
  • Bone Marrow / immunology
  • CHO Cells
  • Cell Line
  • Cricetinae
  • Cricetulus
  • Flow Cytometry
  • HEK293 Cells
  • Humans
  • Immunoglobulin G / immunology*
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Palatine Tonsil / immunology
  • Protein Isoforms / genetics
  • Protein Isoforms / immunology
  • Rats
  • Rats, Wistar
  • Receptors, IgG / biosynthesis*
  • Receptors, IgG / immunology*
  • Spleen / immunology

Substances

  • Antibodies, Monoclonal
  • Immunoglobulin G
  • Protein Isoforms
  • Receptors, IgG