Zhang Chenyun, Liu Haizhou
School of Medicine, University of Tsinghua, Beijing, China.
Division of Hematology-Oncology, Department of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
J Immunol Res. 2025 Jan 15;2025:5845167. doi: 10.1155/jimr/5845167. eCollection 2025.
In recent years, chimeric antigen receptor T-cell (CAR-T) therapy has made groundbreaking progress in the treatment of various cancer types, particularly hematological malignancies. In the meantime, various preclinical and clinical studies have extensively explored dual-target CAR-T therapies which can be designed to recognize two antigens simultaneously based on the immunophenotype of tumor cells. Compared with single-target CAR-T approach, dual-target CAR-T therapies demonstrate varying degrees of superior antitumor CAR effects, prevent antigen escape and relapse, reduce on-target off-tumor effects, and ensure durable responses in different types of cancer. These advantages highlight the potential future prospects in this field, showing varying degrees of advancement in preclinical and clinical studies. Herein, we aimed to review different dual-target CAR-T studies conducted on a wide range of tumor models, summarizing the selection of target combinations, the efficacy and safety demonstrated in preclinical and clinical settings, the existing limitations, and the potential future directions of this promising therapeutic strategy.
近年来,嵌合抗原受体T细胞(CAR-T)疗法在各种癌症类型的治疗中取得了突破性进展,尤其是血液系统恶性肿瘤。与此同时,各种临床前和临床研究广泛探索了双靶点CAR-T疗法,这种疗法可根据肿瘤细胞的免疫表型设计为同时识别两种抗原。与单靶点CAR-T方法相比,双靶点CAR-T疗法显示出不同程度的更优抗肿瘤CAR效应,可防止抗原逃逸和复发,减少脱靶效应,并确保在不同类型癌症中产生持久反应。这些优势凸显了该领域未来的潜在前景,在临床前和临床研究中均展现出不同程度的进展。在此,我们旨在综述针对广泛肿瘤模型开展的不同双靶点CAR-T研究,总结靶点组合的选择、临床前和临床环境中显示的疗效和安全性、存在的局限性以及这种有前景的治疗策略未来的潜在方向。