基础医学与临床 ›› 2025, Vol. 45 ›› Issue (5): 675-680.doi: 10.16352/j.issn.1001-6325.2025.05.0675

• 短篇综述 • 上一篇    下一篇

多靶点CAR-T细胞疗法在急性B淋巴细胞白血病中的应用

曹金金1, 杜娟1, 瞿姗娜1, 朱明宇1, 汪洋1, 胡翰1, 刘滨磊1,2*   

  1. 1.湖北工业大学 生命科学与健康工程学院,湖北 武汉 430068;
    2.武汉滨会生物科技股份有限公司,湖北 武汉 436030
  • 收稿日期:2024-12-13 修回日期:2025-03-18 出版日期:2025-05-05 发布日期:2025-04-23
  • 通讯作者: * liubl@hbut.edu.cn
  • 基金资助:
    国家自然科学基金青年科学基金(82001758)

Application of multi-targeted CAR-T cell therapy in B-cell acute lymphoblastic leukemia

CAO Jinjin1, DU Juan1, QU Shanna1, ZHU Mingyu1, WANG Yang1, HU Han1, LIU Binlei1,2*   

  1. 1. School of Life and Health Sciences, Hubei University of Technology, Wuhan 430068;
    2. Wuhan Binhui Biopharmaceutical Co. , Ltd. , Wuhan 436030, China
  • Received:2024-12-13 Revised:2025-03-18 Online:2025-05-05 Published:2025-04-23
  • Contact: * liubl@hbut.edu.cn

摘要: 嵌合抗原受体T(CAR-T)细胞疗法作为一种新型细胞免疫疗法,在治疗恶性血液瘤尤其是急性B淋巴细胞白血病的临床上已经展现出较好的疗效。然而,单一靶点选择存在抗原丧失和免疫逃逸等问题,因此多靶点治疗策略逐渐受到关注。多靶点CAR-T是通过同时靶向多个肿瘤相关抗原,既能有效避免单一靶点导致的抗原逃逸问题,降低了复发风险,又有望提高治疗效果。本文主要介绍了多靶点CAR-T细胞疗法的结构类型以及治疗急性B淋巴细胞白血病的临床试验应用,期望在未来为治疗急性B淋巴细胞白血病提供参考。

关键词: 多靶点, CAR-T细胞疗法, 急性B淋巴细胞白血病, 脱靶效应, 肿瘤相关抗原

Abstract: Chimeric antigen receptor-modified T (CAR-T) cell therapy, as a new type of cellular immunotherapy, has shown good clinical efficacy in the treatment of malignant hematological tumors, especially B-cell acute lymphoblastic leukemia. However, there are problems such as antigen loss and immune evasion in single-target selection, so multi-target therapy strategies are gradually gaining attention. Multi-target CAR-T can effectively avoid antigen escape caused by a single target by targeting multiple tumor-associated antigens at the same time, reduce the risk of recurrence, and is expected to improve the therapeutic effect. This paper primarily discusses the structural types of multi-target CAR-T cell therapy and its clinical trial applications in the treatment of B-cell acute lymphoblastic leukemia (B-ALL), aiming to provide future references for the treatment of B-ALL.

Key words: multi-target, CAR-T cell therapy, B-cell acute lymphoblastic leukemia, off-target effect, tumor-associated antigen

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