Murray J S
Dept of Microbiology, University of Kansas, Lawrence 66045, USA.
Immunol Today. 1998 Apr;19(4):157-63. doi: 10.1016/s0167-5699(97)01237-1.
While the effects of cytokines on T helper 1 (Th1)/Th2 differentiation are well documented, it is less clear why a dichotomy of effector cytokine production would initiate from antigen-specific lymphocytes. Nevertheless, in defined experimental systems, the interaction between T-cell receptor (TCR), peptide and major histocompatibility complex (MHC) can determine Th1/Th2 dominance. Here, Joseph Murray discusses how TCR affinity and ligand density might interface with innate forces in the selection of CD4+ T-cell functions.
虽然细胞因子对辅助性T细胞1(Th1)/Th2分化的影响已有充分记载,但尚不清楚为什么效应细胞因子的产生会从抗原特异性淋巴细胞开始出现二分法。然而,在特定的实验系统中,T细胞受体(TCR)、肽和主要组织相容性复合体(MHC)之间的相互作用可以决定Th1/Th2的主导地位。在此,约瑟夫·默里讨论了TCR亲和力和配体密度在选择CD4+T细胞功能时如何与固有因素相互作用。