Department of Microbiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Department of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania.
Am J Hematol. 2019 May;94(S1):S3-S9. doi: 10.1002/ajh.25418. Epub 2019 Feb 18.
Chimeric antigen receptor (CAR) T-cell therapy represents a major advancement in personalized cancer treatment. In this strategy, a patient's own T cells are genetically engineered to express a synthetic receptor that binds a tumor antigen. CAR T cells are then expanded for clinical use and infused back into the patient's body to attack and destroy chemotherapy-resistant cancer. Dramatic clinical responses and high rates of complete remission have been observed in the setting of CAR T-cell therapy of B-cell malignancies. This resulted in two recent FDA approvals of CAR T cells directed against the CD19 protein for treatment of acute lymphoblastic leukemia and diffuse large B-cell lymphoma. Thus, CAR T cells are arguably one of the first successful examples of synthetic biology and personalized cellular cancer therapy to become commercially available. In this review, we introduce the concept of using CAR T cells to break immunological tolerance to tumors, highlight several challenges in the field, discuss the utility of biomarkers in the context of predicting clinical responses, and offer prospects for developing next-generation CAR T cell-based approaches that will improve outcome.
嵌合抗原受体 (CAR) T 细胞疗法代表了个性化癌症治疗的重大进展。在该策略中,患者自身的 T 细胞经过基因工程改造,表达一种合成受体,该受体可与肿瘤抗原结合。然后对 CAR T 细胞进行扩增,用于临床,并回输到患者体内,以攻击和破坏化疗耐药的癌症。在 CAR T 细胞治疗 B 细胞恶性肿瘤的情况下,观察到了显著的临床反应和高完全缓解率。这导致最近 FDA 批准了两种针对 CD19 蛋白的 CAR T 细胞用于治疗急性淋巴细胞白血病和弥漫性大 B 细胞淋巴瘤。因此,可以说 CAR T 细胞是合成生物学和个性化细胞癌症治疗首次成功商业化的范例之一。在这篇综述中,我们介绍了使用 CAR T 细胞打破对肿瘤的免疫耐受的概念,强调了该领域的几个挑战,讨论了生物标志物在预测临床反应方面的应用,并对开发下一代基于 CAR T 细胞的方法提供了前景,这些方法将改善治疗结果。