T细胞受体
抗原
T细胞
肿瘤微环境
免疫学
癌症研究
肿瘤抗原
免疫疗法
医学
生物
免疫系统
作者
Dandan Yang,Zhihui Duan,Ping Yuan,Chengming Ding,Jianjun Zou,Guodong Chen,Daichao Wu
标识
DOI:10.1016/j.bbrc.2023.149209
摘要
TCR-engineered T cells have achieved great progress in solid tumor therapy, some of which have been applicated in clinical trials. Deep knowledge about the current progress of TCR-T in tumor therapy would be beneficial to understand the direction. Here, we classify tumor antigens into tumor-associated antigens, tumor-specific antigens, tumor antigens expressed by oncogenic viruses, and tumor antigens caused by abnormal protein modification; Then we detail the TCR-T cell therapy effects targeting those tumor antigens in clinical or preclinical trials, and propose that neoantigen specific TCR-T cell therapy is expected to be a promising approach for solid tumors; Furthermore, we summarize the optimization strategies, such as tumor microenvironment, TCR pairing and affinity, to improve the therapeutic effect of TCR-T. Overall, this review provides inspiration for the antigen selection and therapy strategies of TCR-T in the future.
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