Department of Immunology and Microbiology, University of Colorado School of Medicine, Aurora, Colorado.
Mol Carcinog. 2020 Jul;59(7):862-870. doi: 10.1002/mc.23212. Epub 2020 May 9.
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.
T 细胞受体 (TCRs) 与其配体——肽/主要组织相容性复合体复合物 (pMHCs) 之间的相互作用强度是当今免疫肿瘤学中讨论和研究最多的 T 细胞特征之一。尽管 T 细胞表面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这种相互作用发生的环境是决定 T 细胞如何反应的关键。与肿瘤相关抗原相互作用的 T 细胞的 TCR 库虽然通常亲和力较低,但却非常广泛。在这里,我们重点关注 CD8+ T 细胞的 TCR 与免疫肿瘤学中使用的不同模型之间的低亲和力相互作用。