CD19嵌合抗原受体T细胞治疗后白血病复发的遗传机制

Cancer biotherapy & radiopharmaceuticals Pub Date : 2022-06-01 Epub Date: 2021-03-18 DOI:10.1089/cbr.2020.4630
Songlin Qiu, Ye Pan, Shenyan Shi, Fapohunda Funmilayo Omotoyosi, Keping Chen, Zhigang Guo, Peng Lü
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引用次数: 1

摘要

嵌合抗原受体T细胞疗法(CART)在过去10年中治疗白血病取得了优异的效果。抗cd19 CART治疗B细胞急性淋巴细胞白血病可达到90%的完全缓解率。虽然CART极大地改善了白血病和淋巴瘤患者的治疗,但多达三分之一的患者在CART后会出现疾病复发。肿瘤表面标志物CD19在大多数复发患者中呈阴性,这些患者在治疗前CD19呈高表达。本文就目前CD19 CART治疗白血病后CD19阴性复发的原因及靶逃逸的机制作一综述。并讨论了治疗复发的方法和策略,为白血病复发的治疗提供参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genetic Mechanism of Leukemia Relapse Following CD19 Chimeric Antigen Receptor T Cell Therapy.

Chimeric antigen receptor T cell therapy (CART) has achieved excellent results in the past 10 years for treating of leukemia. Treatment of B cell acute lymphoblastic leukemia by anti-CD19 CART can reach a complete remission rate of 90%. Although CART has greatly improved the treatment of patients with leukemia and lymphoma, as many as one-third of the patients can suffer disease relapse after CART. The tumor surface marker CD19 is negative in most the patients who relapse, and these patients display high expression of CD19 before treatment. In this review, the current causes of CD19-negative relapses after CD19 CART against leukemia, and the mechanisms of target escape are briefly summarized. Also, methods and strategies for treating relapse to provide references for the treatment of leukemia relapse are also discussed.

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