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

机译:我们如何满足嵌合抗原受体T细胞治疗实体瘤的挑战?

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摘要

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.
机译:免疫检查点抑制极大地改善了实体瘤的治疗,但大多数患者没有获得持久的临床益处,因此需要新的免疫治疗方法。通过基因工程表达嵌合抗原受体(CARs)的自体T细胞在血液系统恶性肿瘤方面取得了前所未有的临床成功,目前正在积极努力将这些益处转化为实体瘤领域。然而,实体瘤对CAR T细胞的发育提出了独特的挑战。在这篇综述中,我们检查了进展的潜在障碍,并介绍了在实体瘤中使用CAR疗法克服这些挑战的新方法。

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