George Andrew J T, Stark Jaroslav, Chan Cliburn
Department of Immunology, Division of Medicine, Faculty of Medicine, Imperial College London, Hammersmith Campus, Du Cane Road, London, UK W12 0NN.
Trends Immunol. 2005 Dec;26(12):653-9. doi: 10.1016/j.it.2005.09.011. Epub 2005 Oct 17.
The response of T cells to antigen shows an amazing degree of both sensitivity and specificity, with a cell responding to 1-10 peptide-MHC complexes and being sensitive to single amino acid substitutions. Kinetic proofreading or feedback pathways achieve specificity at the level of the receptor, whereas serial engagement of receptors by ligand molecules enhances sensitivity. Crosstalk between receptors, integration of signals and/or tuning of responses is important at the level of the cell. Induction of anergic or regulatory cells by suboptimal stimuli prevents cell activation by multiple encounters with weak ligands. Thus, for optimal sensitivity and specificity, it is necessary to have mechanisms that operate at the level of the receptor, the cell and finally, the population of responding cells.
T细胞对抗原的反应表现出惊人的敏感性和特异性,一个细胞能对1至10个肽 - 主要组织相容性复合体(peptide-MHC)作出反应,并且对单个氨基酸替换敏感。动力学校对或反馈途径在受体水平实现特异性,而配体分子与受体的连续结合则增强敏感性。受体之间的相互作用、信号整合和/或反应调节在细胞水平很重要。次优刺激诱导无反应性或调节性细胞可防止细胞因多次接触弱配体而被激活。因此,为了实现最佳的敏感性和特异性,有必要具备在受体水平、细胞水平以及最终在反应性细胞群体水平起作用的机制。