Co-signal Molecules in T-Cell Activation

被引:44
|
作者
Azuma, Miyuki [1 ]
机构
[1] Tokyo Med & Dent Univ, Grad Sch Med & Dent Sci, Dept Mol Immunol, Tokyo, Japan
关键词
Co-signals; Co-stimulation; Co-inhibition; T-cell activation; Two-signal model; Tolerance; B7; FAMILY-MEMBER; CTLA-4; COUNTER-RECEPTOR; IN-VIVO; INHIBITORY RECEPTOR; TNF RECEPTOR; COSTIMULATORY MOLECULES; LYMPHOCYTE ATTENUATOR; ANTIGEN PRESENTATION; CHECKPOINT BLOCKADE; PROGRAMMED DEATH-1;
D O I
10.1007/978-981-32-9717-3_1
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The two-signal model of T-cell activation, proposed approximately four decades ago, has undergone various refinements while maintaining its principal doctrine. Since the discovery of CD28, a variety of co-signal molecules, including co-stimulatory and co-inhibitory receptors and ligands, have been identified. These molecules fine-tune various immune responses both in the primary or secondary lymphoid tissues and in the peripheral tissues. Most co-signal receptors are expressed and induced on T cells during distinct stages (naive/resting, activating, memory, and exhausting). These co-signaling pathways play critical and diverse roles in maintaining T-cell tolerance and eliciting T-cell immune responses in health and disease. This introductory chapter provides a historical overview of the key findings that have led to our current view of T-cell co-stimulation.
引用
收藏
页码:3 / 23
页数:21
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