| Literature DB >> 28463043 |
Gillian Dekkers1, Arthur E H Bentlage1, Tamara C Stegmann1, Heather L Howie2, Suzanne Lissenberg-Thunnissen1, James Zimring2, Theo Rispens3, Gestur Vidarsson1.
Abstract
Human IgG is the main antibody class used in antibody therapies because of its efficacy and longer half-life, which are completely or partly due to FcγR-mediated functions of the molecules. Preclinical testing in mouse models are frequently performed using human IgG, but no detailed information on binding of human IgG to mouse FcγRs is available. The orthologous mouse and human FcγRs share roughly 60-70% identity, suggesting some incompatibility. Here, we report binding affinities of all mouse and human IgG subclasses to mouse FcγR. Human IgGs bound to mouse FcγR with remarkably similar binding strengths as we know from binding to human ortholog receptors, with relative affinities IgG3>IgG1>IgG4>IgG2 and FcγRI>>FcγRIV>FcγRIII>FcγRIIb. This suggests human IgG subclasses to have similar relative FcγR-mediated biological activities in mice.Entities:
Keywords: Fc-receptors; FcγR; IgG subclasses; mouse models; surface plasmon resonance
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Year: 2017 PMID: 28463043 PMCID: PMC5524164 DOI: 10.1080/19420862.2017.1323159
Source DB: PubMed Journal: MAbs ISSN: 1942-0862 Impact factor: 5.857