The T cell surface protein, CD28

被引:9
作者
Edmead, CE
Lamb, JR
Hoyne, GF
机构
[1] Infection and Immunity Section, Department of Biology, Imp. Coll. Sci., Technol. and Med., London SW7 2BB, Prince Consort Road
关键词
CD28; costimulation; anergy; T cell activation;
D O I
10.1016/S1357-2725(97)00012-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
The cluster of differentiation (CD) antigen CD28 is a 44-kDa, disulphide-bonded, homodimeric glycoprotein, which is constitutively expressed on the surface of all murine T cells and the majority of human T cells. Ligation of CD28 by its counter receptor, B7, expressed on the surface of antigen presenting cells, has been shown to induce signals that, in synergy with those derived from engagement of the T cell receptor by an antigen bound to a major histocompatibility complex, enhance proliferation and cytokine production. Manipulation of this interaction can have dramatic effects on the outcome of T cell activation. Blocking CD28/B7 interactions may be useful in preventing unwanted activation in allergy and autoimmune diseases, whereas enhancing this interaction can promote tumour rejection. Thus, CD28 and its signalling pathways may prove to be useful targets in the development of new therapeutic treatments. (C) 1997 Elsevier Science Ltd.
引用
收藏
页码:1053 / 1057
页数:5
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