Structural basis of T cell recognition of peptides bound to MHC molecules

被引:73
作者
Wang, JH
Reinherz, EL
机构
[1] Dana Farber Canc Inst, Immunobiol Lab, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Pediat, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Dept Biol Chem & Mol Pharmacol, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Dept Med, Boston, MA USA
关键词
T cell receptor; alloreactivity; MHC class II; structure; thymic selection;
D O I
10.1016/S0161-5890(02)00033-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Helper T lymphocytes play a critical role in immune system activation following recognition of MHC class II-bound peptide ligands (pMHCII). These CD4 T cells stimulate B cell antibody production and cytolytic T cell generation. Until recently. the structural basis of coordinate T cell receptor (TCR) and CD4 co-receptor interaction with a given was unknown. Here we review current structural data on specific pMHCII recognition by T cells and compare TCR and co-receptor docking to pMHCI versus pMHCII ligands. The implications of these findings for thymic selection. helper versus cytoltic T cell recognition and alloreactivity are discussed. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1039 / 1049
页数:11
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