Zhang Bohan, Wu Jiawen, Jiang Hua, Zhou Min
State Key Laboratory of Systems Medicine for Cancer, Shanghai Cancer Institute, Renji Hospital, Shanghai Jiaotong University School of Medicine, Shanghai 200032, China.
CARsgen Therapeutics, Shanghai 200231, China.
Cells. 2025 Feb 20;14(5):320. doi: 10.3390/cells14050320.
Chimeric antigen receptor (CAR) gene-modified T-cell therapy has achieved significant success in the treatment of hematological malignancies. However, this therapy has not yet made breakthroughs in the treatment of solid tumors and still faces issues of resistance and relapse in hematological cancers. A major reason for these problems is the antigenic heterogeneity of tumor tissues. This review outlines the antigenic heterogeneity encountered in CAR-T cell therapy and the corresponding strategies to address it. These strategies include using combination therapy to increase the abundance of target antigens, optimizing the structure of CARs to enhance sensitivity to low-density antigens, developing multi-targeted CAR-T cells, and reprogramming the TME to activate endogenous immunity. These approaches offer new directions for overcoming tumor antigenic heterogeneity in CAR-T cell therapy.
嵌合抗原受体(CAR)基因修饰的T细胞疗法在血液系统恶性肿瘤的治疗中取得了显著成功。然而,这种疗法在实体瘤治疗方面尚未取得突破,并且在血液系统癌症中仍面临耐药性和复发问题。这些问题的一个主要原因是肿瘤组织的抗原异质性。本综述概述了CAR-T细胞疗法中遇到的抗原异质性以及应对该问题的相应策略。这些策略包括使用联合疗法增加靶抗原的丰度、优化CAR结构以增强对低密度抗原的敏感性、开发多靶点CAR-T细胞以及重编程肿瘤微环境以激活内源性免疫。这些方法为克服CAR-T细胞疗法中的肿瘤抗原异质性提供了新方向。