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T-cell receptor affinity in the age of cancer immunotherapy.
Molecular Carcinogenesis ( IF 4.6 ) Pub Date : 2020-05-09 , DOI: 10.1002/mc.23212
Michele M Hoffmann 1 , Jill E Slansky 1
Affiliation  

The strength of the interaction between T‐cell receptors (TCRs) and their ligands, peptide/major histocompatibility complex complexes (pMHCs), is one of the most frequently discussed and investigated features of T cells in immuno‐oncology today. Although there are many molecules on the surface of T cells that interact with ligands on other cells, the TCR/pMHC is the only receptor‐ligand pair that offers antigen specificity and dictates the functional response of the T cell. The strength of the TCR/pMHC interaction, along with the environment in which this interaction takes place, is key to how the T cell will respond. The TCR repertoire of T cells that interact with tumor‐associated antigens is vast, although typically of low affinity. Here, we focus on the low‐affinity interactions between TCRs from CD8+ T cells and different models used in immuno‐oncology.

中文翻译:

癌症免疫治疗时代的T细胞受体亲和力。

T细胞受体(TCR)与它们的配体,肽/主要组织相容性复合物(pMHCs)之间的相互作用强度是当今免疫肿瘤学中最经常讨论和研究的T细胞特征之一。尽管T细胞表面上有许多与其他细胞上的配体相互作用的分子,但TCR / pMHC是唯一提供抗原特异性并决定T细胞功能反应的受体-配体对。TCR / pMHC相互作用的强度以及发生这种相互作用的环境,是T细胞反应方式的关键。与肿瘤相关抗原相互作用的T细胞的TCR库很大,尽管亲和力通常很低。这里,
更新日期:2020-05-09
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