A molecular perspective of CTLA-4 function

被引:423
作者
Teft, Wendy A. [1 ]
Kirchhof, Mark G.
Madrenas, Joaquin
机构
[1] Univ Western Ontario, Robarts Res Inst, FOCIS Ctr Clin Immunol & Immunotherapeut, London, ON N6A 5K8, Canada
[2] Univ Western Ontario, Dept Microbiol & Immunol, London, ON N6A 5K8, Canada
[3] Univ Western Ontario, Dept Med, London, ON N6A 5K8, Canada
关键词
costimulation; T cell activation; immunological synapse; PP2A; B7; signal plasticity;
D O I
10.1146/annurev.immunol.24.021605.090535
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Within the paradigm of the two-signal model of lymphocyte activation, the interest in costimulation has witnessed a remarkable emergence in the past few years with the discovery of a large array of molecules that can serve this role, including some with an inhibitory function. Interest has been further enhanced by the realization of these molecules' potential as targets to modulate clinical immune responses. Although the therapeutic translation of mechanistic knowledge in costimulatory molecules has been relatively straightforward, the capacity to target their inhibitory counterparts has remained limited. This limited capacity is particularly apparent in the case of the cytotoxic T lymphocyte-associated antigen-4 (CTLA-4), a major negative regulator of T cell responses. Because there have been several previous comprehensive reviews on the function of this molecule, we focus here on the physiological implications of its structural features. Such an exercise may ultimately help us to design immunotherapeutic agents that target CTLA-4.
引用
收藏
页码:65 / 97
页数:33
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