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我们如何应对实体瘤嵌合抗原受体 T 细胞疗法的挑战?

How Do We Meet the Challenge of Chimeric Antigen Receptor T-Cell Therapy for Solid Tumors?

机构信息

From the Cellular Therapy Center, Department of Medicine, Memorial Sloan Kettering Cancer Center, and Department of Medicine, Weill Cornell Medical College, New York, NY.

出版信息

Cancer J. 2021;27(2):134-142. doi: 10.1097/PPO.0000000000000516.

Abstract

Immune checkpoint inhibition has vastly improved the treatment of solid tumors, but most patients do not experience durable clinical benefit, so novel immunotherapeutic approaches are needed. Autologous T cells genetically engineered to express chimeric antigen receptors (CARs) have led to unprecedented clinical success in hematologic malignancies, and increasing efforts are actively being pursued to translate these benefits to the solid tumor arena. However, solid tumors present unique challenges for CAR T-cell development. In this review, we examine the potential barriers to progress and present emerging approaches to overcome these challenges with CAR therapy in solid tumors.

摘要

免疫检查点抑制极大地改善了实体瘤的治疗效果,但大多数患者并未获得持久的临床获益,因此需要新的免疫治疗方法。经过基因工程改造表达嵌合抗原受体 (CAR) 的自体 T 细胞在血液恶性肿瘤的治疗中取得了前所未有的临床成功,并且正在积极努力将这些益处转化到实体肿瘤领域。然而,实体瘤的 CAR T 细胞发展存在独特的挑战。在这篇综述中,我们研究了进展的潜在障碍,并提出了使用 CAR 疗法克服实体瘤中这些挑战的新方法。

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