T细胞受体
效应器
T细胞
细胞生物学
主要组织相容性复合体
生物
功能(生物学)
表型
计算生物学
生物物理学
抗原
免疫学
遗传学
免疫系统
基因
作者
Michael A Faust,Viva Jeanne Rase,Tracey J. Lamb,Brian D. Evavold
出处
期刊:Journal of Immunology
[The American Association of Immunologists]
日期:2023-08-01
卷期号:211 (3): 333-342
被引量:5
标识
DOI:10.4049/jimmunol.2300141
摘要
Abstract One of the main goals in T cell biology has been to investigate how TCR recognition of peptide:MHC (pMHC) determines T cell phenotype and fate. Ag recognition is required to facilitate survival, expansion, and effector function of T cells. Historically, TCR affinity for pMHC has been used as a predictor for T cell fate and responsiveness, but there have now been several examples of nonfunctional high-affinity clones and low-affinity highly functional clones. Recently, more attention has been paid to the TCR being a mechanoreceptor where the key biophysical determinant is TCR bond lifetime under force. As outlined in this review, the fundamental parameters between the TCR and pMHC that control Ag recognition and T cell triggering are affinity, bond lifetime, and the amount of force at which the peak lifetime occurs.
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