Wang Jia-huai, Reinherz Ellis L
Laboratory of Immunobiology, Dana-Farber Cancer Institute, 44 Binney Street, Boston, MA 02115, USA.
Mol Immunol. 2002 May;38(14):1039-49. doi: 10.1016/s0161-5890(02)00033-0.
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 pMHCII 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 cytolytic T cell recognition and alloreactivity are discussed.
辅助性T淋巴细胞在识别与II类主要组织相容性复合体(MHC)结合的肽配体(pMHCII)后,在免疫系统激活过程中发挥关键作用。这些CD4 T细胞刺激B细胞产生抗体以及细胞毒性T细胞的生成。直到最近,T细胞受体(TCR)和CD4共受体与特定pMHCII协同相互作用的结构基础仍不清楚。在此,我们综述了目前关于T细胞特异性识别pMHCII的结构数据,并比较了TCR和共受体与pMHCI及pMHCII配体对接的情况。还讨论了这些发现对胸腺选择、辅助性T细胞与细胞毒性T细胞识别以及同种异体反应性的影响。