胶质母细胞瘤的嵌合抗原受体T细胞:未来之旅

Glioma Pub Date : 2019-03-01 DOI:10.4103/glioma.glioma_6_19
S. Joseph, N. Ahmed, M. Hegde
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引用次数: 0

摘要

嵌合抗原受体(CARs)是一种基因工程化的跨膜细胞受体,由与激活的细胞内T细胞信号链融合的抗原结合外结构域组成。将CAR分子移植到T细胞上可以靶向杀伤肿瘤。用CARs修饰自体患者免疫细胞的基因治疗方法现在已经从研究台转移到难治性、复发性和无复发性胶质母细胞瘤患者的早期临床试验。这是对CAR T细胞治疗胶质母细胞瘤领域的科学现状的回顾,也是临床试验注册处(www.clinicaltrials.gov)已完成和正在进行的临床试验的最新情况。在这里,我们还讨论了从CAR T淋巴细胞治疗胶质母母细胞瘤的临床试验中获得的见解,以及提高其疗效的创新方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Chimeric antigen receptor T-cells for glioblastoma: The journey ahead
Chimeric antigen receptors (CARs) are genetically engineered transmembrane cell receptors consisting of an antigen-binding ectodomain fused to an activating intracellular T-cell signaling chain. Grafting CAR molecules on T-cells enables targeted killing of tumors. The gene therapy approach of modifying autologous patient immune cells with CARs has now moved from the research bench to early-phase clinical trials in patients with refractory, recurrent, and nonresectable glioblastoma. This is a review of the state of the science in the field of CAR T-cells for glioblastoma and an update on the completed and ongoing clinical trials available at the Clinical Trials Registry (www.clinicaltrials.gov). Here, we also discuss insights gained from the clinical trials of CAR T-cells against glioblastoma and innovative approaches to improve their efficacy.
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