CTLA-4 co-receptor impacts on the function of Treg and CD8+ T-cell subsets.

作者信息

Rudd Christopher E

机构信息

Department of Pathology, Cell Signalling Section, University of Cambridge, Cambridge, UK.

出版信息

Eur J Immunol. 2009 Mar;39(3):687-90. doi: 10.1002/eji.200939261.

Abstract

CTLA-4 has potent regulatory effects on the threshold of T-cell signalling and, in the process, guards against the development of hyper-proliferation and autoimmunity. Despite this, the role of CTLA-4 on specific T-cell subsets has been unclear. Such studies could shed light on both the function of CTLA-4, and on the contribution of the subsets to the disease phenotype of the Ctla4(-/-) mouse. Recently, a role for this co-receptor in the function of Treg has been outlined and, in this issue of the European Journal of Immunology, the selective targeting of the T-box transcription factor Eomes by CTLA-4 in the regulation of CD8(+) cytolytic T-cell (CTL) effector function is shown. Together, these papers shed light on the role of CTLA-4 in different T-cell subsets.

摘要

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