Novel roles for complement receptors in T cell regulation and beyond

Claudia Kemper*, Jörg Köhl

*Corresponding author for this work
65 Citations (Scopus)

Abstract

Complement receptors are expressed on cells of the innate and the adaptive immune system. They play important roles in pathogen and danger sensing as they translate the information gathered by complement fluid phase sensors into cellular responses. Further, they control complement activation on viable and apoptotic host cells, clearance of immune complexes and mediate opsonophagocytosis. More recently, evidence has accumulated that complement receptors form a complex network with other innate receptors systems such as the Toll-like receptors, the Notch signaling system, IgG Fc receptors and C-type lectin receptors contributing to the benefit and burden of innate and adaptive immune responses in autoimmune and allergic diseases as well as in cancer and transplantation. Here, we will discuss recent developments and emerging concepts of complement receptor activation and regulation with a particular focus on the differentiation, maintenance and contraction of effector and regulatory T cells.

Original languageEnglish
JournalMolecular Immunology
Volume56
Issue number3
Pages (from-to)181-190
Number of pages10
ISSN0161-5890
DOIs
Publication statusPublished - 05.12.2013

Funding

We thank Drs. Gaelle Le Friec and Martin Kolev for their critical comments on the manuscript and Dr. Christian M. Karsten for his help with illustrations. Research in the Kemper laboratory is supported by an MRC grant ( G1002165 ) and by the National Institute for Health Research (NIHR) Biomedical Research Centre based at Guy's and St Thomas’ NHS Foundation Trust and King's College London . The views expressed are those of the author(s) and not necessarily those of the NHS, the NIHR or the Department of Health. C.K. acknowledges the support of the MRC Centre for Transplantation. Research in the Köhl laboratory is supported by Deutsche Forschungsgemeinschaft (DFG) grants EXC306 , SFB/TR22 , SFB654 , IRTG 1911 , GRK1727 and KO 1245-3/1 to J.K. The authors declare no competing financial interests.

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