Du Shi, Yan Jingyue, Xue Yonger, Zhong Yichen, Dong Yizhou
Division of Pharmaceutics and Pharmacology College of Pharmacy Ohio State University Columbus USA.
Icahn Genomics Institute Precision Immunology Institute Department of Oncological Sciences Tisch Cancer Institute Friedman Brain Institute Icahn School of Medicine at Mount Sinai New York USA.
Exploration (Beijing). 2023 Jul 2;3(4):20210058. doi: 10.1002/EXP.20210058. eCollection 2023 Aug.
Adoptive cell therapy (ACT) is a rapidly growing anti-cancer strategy that has shown promise in treating various cancer types. The concept of ACT involves activating patients' own immune cells ex vivo and then transferring them back to the patients to recognize and eliminate cancer cells. Currently, the commonly used ACT includes tumor-infiltrating lymphocytes (TILs), genetically engineered immune cells, and dendritic cells (DCs) vaccines. With the advancement of cell culture and genetic engineering techniques, ACT has been used in clinics to treat malignant hematological diseases and many new ACT-based regimens are in different stages of clinical trials. Here, representative ACT approaches are introduced and the opportunities and challenges for clinical translation of ACT are discussed.
过继性细胞疗法(ACT)是一种迅速发展的抗癌策略,已在治疗多种癌症类型方面显示出前景。ACT的概念包括在体外激活患者自身的免疫细胞,然后将其回输到患者体内以识别和消除癌细胞。目前,常用的ACT包括肿瘤浸润淋巴细胞(TILs)、基因工程免疫细胞和树突状细胞(DCs)疫苗。随着细胞培养和基因工程技术的进步,ACT已在临床上用于治疗恶性血液疾病,并且许多基于ACT的新方案正处于临床试验的不同阶段。在此,介绍了代表性的ACT方法,并讨论了ACT临床转化的机遇和挑战。