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Development and Characterization of Monoclonal Antibodies Specific for Mouse and Human Fcγ Receptors
Author(s) -
Alison L. Tutt,
Sonya James,
Stéphanie A. Laversin,
Thomas Tipton,
Margaret AshtonKey,
Ruth R. French,
Khiyam Hussain,
Andrew Vaughan,
Lang Dou,
Alexander Earley,
Lekh N. Dahal,
Chen Lu,
Melanie Dunscombe,
H. T. Claude Chan,
Christine A. Penfold,
Jinny H Kim,
Elizabeth A. Potter,
C. Ian Mockridge,
Ali Roghanian,
Robert J. Oldham,
Kerry L. Cox,
Sean H. Lim,
Ingrid Teige,
Björn Frendéus,
Martin J. Glennie,
Stephen A. Beers,
Mark S. Cragg
Publication year - 2015
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.1402988
Subject(s) - monoclonal antibody , receptor , antibody , computational biology , biology , immunology , biochemistry
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.

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