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Chimeric Antigen Receptor T Cells for B-Cell Acute Lymphoblastic Leukemia

机译:B细胞急性淋巴细胞白血病的嵌合抗原受体T细胞

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摘要

Chimeric antigen receptor (CAR) T-cell therapy is transforming the landscape for treatment of B-lineage acute lymphoblastic leukemia (B-ALL). Chimeric antigen receptor T-cell therapy makes use of T cells that have been modified to target a cancer-specific cell surface antigen. There is currently 1 Food and Drug Administration-approved CD19-directed CAR T-cell therapy for relapsed/refractory B-ALL with numerous other CAR T-cell products under clinical investigation. This review covers the development of CAR T cells for B-ALL, citing the remarkable efficacy of inducing remissions in a very high-risk population of patients. However, following the first round of CAR T-cell trials targeting CD19 in B-ALL, it has been found that approximately 50% of patients who initially respond will ultimately recur. Current efforts in the field are focusing on the identification of targets beyond CD19 as well as advancing strategies to promote more durable remissions as work is ongoing to move this therapy upfront.
机译:嵌合抗原受体(汽车)T细胞疗法正在转化景观以治疗B族型急性淋巴细胞白血病(B-全部)。嵌合抗原受体T细胞疗法利用已被修饰的T细胞靶向靶癌细胞表面抗原。目前有1种食品和药物管理局批准的CD19针对CD19型汽车T细胞疗法,用于复发/难治性B-全部,其中临床调查下的其他其他汽车T细胞产品。本综述涵盖了B-全部的Car T细胞的开发,涉及在非常高风险患者中诱导戒除的显着疗效。然而,在靶向CD19的第一轮汽车T细胞试验之后,已经发现,大约50%的初始回应的患者最终会发生重搏。本领域目前的努力专注于识别CD19之外的目标,以及推进促进更耐用的除款的策略,因为工作正在进行前期移动此疗法。

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