免疫疗法
T细胞受体
癌症免疫疗法
抗原
单克隆抗体
嵌合抗原受体
癌症研究
免疫系统
T细胞
免疫学
生物
抗体
作者
Qijie Zhao,Yu Jiang,Shixin Xiang,Parham Jabbarzadeh Kaboli,Jing Shen,Yueshui Zhao,Xu Wu,Fukuan Du,Mingxing Li,Chi Hin Cho,Jing Li,Qinglian Wen,Tao Liu,Tao Yi,Zhangang Xiao
标识
DOI:10.3389/fimmu.2021.658753
摘要
This review provides insight into the role of engineered T-cell receptors (TCRs) in immunotherapy. Novel approaches have been developed to boost anticancer immune system, including targeting new antigens, manufacturing new engineered or modified TCRs, and creating a safety switch for endo-suicide genes. In order to re-activate T cells against tumors, immune-mobilizing monoclonal TCRs against cancer (ImmTAC) have been developed as a novel class of manufactured molecules which are bispecific and recognize both cancer and T cells. The TCRs target special antigens such as NY-ESO-1, AHNAK S2580F or ERBB2 H473Y to boost the efficacy of anticancer immunotherapy. The safety of genetically modified T cells is very important. Therefore, this review discusses pros and cons of different approaches, such as ImmTAC, Herpes simplex virus thymidine kinase (HSV-TK), and inducible caspase-9 in cancer immunotherapy. Clinical trials related to TCR-T cell therapy and monoclonal antibodies designed for overcoming immunosuppression, and recent advances made in understanding how TCRs are additionally examined. New approaches that can better detect antigens and drive an effective T cell response are discussed as well.
科研通智能强力驱动
Strongly Powered by AbleSci AI