CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Correlative studies reveal factors contributing to successful CAR-T cell therapies in cancer.
Correlative studies reveal factors contributing to successful CAR-T cell therapies in cancer.
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过去数十年,细胞免疫疗法和靶向免疫疗法改变了癌症治疗。成功的细胞疗法既需要免疫细胞发挥有效且持久的细胞毒作用,也要求靶癌细胞能够被接触并易于应答。临床试验的相关性研究及FDA获批疗法的真实世界数据,揭示了影响细胞疗法缓解率和复发的免疫细胞及癌细胞因素,为研究带来宝贵见解。本综述聚焦具有代表性的工程化CAR-T 细胞(CAR-T 细胞)疗法。在CAR-T 细胞方面,我们讨论与T细胞表型、转录组、表观遗传学、细胞因子信号和代谢相关的发现,这些发现有助于优化细胞制备流程,生产效力和持久性更强的CAR-T 细胞。在癌细胞方面,我们讨论由突变、选择性剪接、转录后修饰及细胞重编程导致的耐药和复发机制。为进一步优化多种恶性肿瘤的细胞疗法,仍需持续开展相关性和机制研究。
Cellular and targeted immunotherapies have revolutionized cancer treatments in the last several decades. Successful cellular therapies require both effective and durable cytotoxic activity from the immune cells as well as an accessible and susceptible response from targeted cancer cells. Correlative studies from clinical trials as well as real-world data from FDA-approved therapies have revealed invaluable insights about immune cell factors and cancer cell factors that impact rates of response and relapse to cellular therapies. This review focuses on the flagship cellular therapy of engineered chimeric antigen receptor T-cells (CAR-T cells).
Within the CAR-T cell compartment, we discuss discoveries about T-cell phenotype, transcriptome, epigenetics, cytokine signaling, and metabolism that inform the cell manufacturing process to produce the most effective and durable CAR-T cells.
Within the cancer cell compartment, we discuss mechanisms of resistance and relapse caused by mutations, alternative splicing, post-transcriptional modifications, and cellular reprogramming. Continued correlative and mechanistic studies are required to help us further optimize cellular therapies in a variety of malignancies.
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