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Low-affinity Fcγ receptors, autoimmunity and infection

Published online by Cambridge University Press:  13 August 2009

Lisa C. Willcocks
Affiliation:
Cambridge Institute for Medical Research and Department of Medicine, University of Cambridge School of Clinical Medicine, Addenbrooke's Hospital, Cambridge, CB2 0XY, UK.
Kenneth G.C. Smith
Affiliation:
Cambridge Institute for Medical Research and Department of Medicine, University of Cambridge School of Clinical Medicine, Addenbrooke's Hospital, Cambridge, CB2 0XY, UK.
Menna R. Clatworthy*
Affiliation:
Cambridge Institute for Medical Research and Department of Medicine, University of Cambridge School of Clinical Medicine, Addenbrooke's Hospital, Cambridge, CB2 0XY, UK.
*
*Corresponding author: Menna R. Clatworthy, Cambridge Institute for Medical Research and Department of Medicine, University of Cambridge School of Clinical Medicine, Addenbrooke's Hospital, Hills Road, Cambridge, CB2 0XY, UK. Tel: +44 1223 762639; Fax: +44 1223 762645; E-mail: [email protected]

Abstract

Low-affinity Fcγ receptors (FcγRs) mediate the effects of immunoglobulin G (IgG) antibodies on leukocytes, including recruitment to inflammatory lesions, phagocytosis, antibody-dependent cellular cytotoxicity, release of inflammatory mediators and regulation of B cell activation. These functions are an important part of the mammalian response to infection, but if deployed inappropriately can cause autoimmune disease. Although most FcγRs are activatory, there is also an inhibitory FcγR that, when bound to IgG immune complexes, is able to downregulate the effects of both the activatory FcγRs and the B cell receptor. This review discusses the role of the low-affinity FcγRs in a balanced immune response and how perturbations in FcγR function result in susceptibility to infection or autoimmunity.

Type
Review Article
Copyright
Copyright © Cambridge University Press 2009

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References

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Further reading, resources and contacts

This homepage for immunologists in Cambridge, UK, gives details of research groups in Cambridge and future immunology meetings:

Nakamura, A., Akiyama, K. and Takai, T. (2005) Fc receptor targeting in the treatment of allergy, autoimmune diseases and cancer. Expert Opinion on Therapeutic Targets 9, 169-190CrossRefGoogle ScholarPubMed
Nimmerjahn, F. and Ravetch, J.V. (2007) Antibodies, Fc receptors and cancer. Current Opinion in Immunology 19, 239-245CrossRefGoogle ScholarPubMed
Elkon, K. and Casali, P. (2008) Nature and functions of autoantibodies. Nature Clinical Practice Rheumatology 4, 491-498CrossRefGoogle ScholarPubMed
Nimmerjahn, F. and Ravetch, J.V. (2008) Anti-inflammatory actions of intravenous immunoglobulin. Annual Review of Immunology 26, 513-533CrossRefGoogle ScholarPubMed
Nakamura, A., Akiyama, K. and Takai, T. (2005) Fc receptor targeting in the treatment of allergy, autoimmune diseases and cancer. Expert Opinion on Therapeutic Targets 9, 169-190CrossRefGoogle ScholarPubMed
Nimmerjahn, F. and Ravetch, J.V. (2007) Antibodies, Fc receptors and cancer. Current Opinion in Immunology 19, 239-245CrossRefGoogle ScholarPubMed
Elkon, K. and Casali, P. (2008) Nature and functions of autoantibodies. Nature Clinical Practice Rheumatology 4, 491-498CrossRefGoogle ScholarPubMed
Nimmerjahn, F. and Ravetch, J.V. (2008) Anti-inflammatory actions of intravenous immunoglobulin. Annual Review of Immunology 26, 513-533CrossRefGoogle ScholarPubMed