Barbra Johnson Sasu, Elvin James Lauron, Thomas Schulz, Hsin-Yuan Cheng, Cesar Sommer
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引用次数: 0
摘要
自体嵌合抗原受体(CAR)T细胞疗法是由患者自身的T细胞产生的,它改变了血液系统恶性肿瘤的治疗格局,但也存在一些弊端,阻碍了大规模临床应用,包括供应方面的物流复杂性、患者T细胞的健康状况、治疗延迟以及生产名额有限。异体 CAR T 细胞疗法或现成的 CAR T 细胞疗法有可能克服自体疗法的许多局限性,为所有符合治疗条件的患者带来益处。这篇综述重点介绍了癌症异体细胞疗法的进展和挑战,以及为提高异体CAR T细胞的持久性和抗肿瘤疗效而在临床前和临床试验中评估的各种方法,包括避免免疫排斥的新策略。《癌症生物学年度综述》第8卷的最终在线出版日期预计为2024年4月。修订后的预计日期请参见 http://www.annualreviews.org/page/journal/pubdates。
Autologous chimeric antigen receptor (CAR) T cell therapy, produced from the patient's own T cells, has changed the treatment landscape for hematologic malignancies but has some drawbacks that prevent large-scale clinical application, including logistical complexities in supply, patient T cell health, treatment delays, and limited manufacturing slots. Allogeneic, or off-the-shelf, CAR T cell therapies have the potential to overcome many of the limitations of autologous therapies, with the aim of bringing benefit to all patients eligible for treatment. This review highlights the progress and challenges of allogeneic cell therapies for cancer and the various approaches that are being evaluated preclinically and in clinical trials to enhance the persistence and antitumor efficacy of allogeneic CAR T cells, including new strategies to avoid immune rejection.Expected final online publication date for the Annual Review of Cancer Biology, Volume 8 is April 2024. Please see http://www.annualreviews.org/page/journal/pubdates for revised estimates.