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[嵌合抗原受体T细胞疗法治疗血液系统恶性肿瘤]

[Chimeric antigen receptor T-cell therapy for hematological malignancies].

作者信息

Nakazawa Yozo

机构信息

Department of Pediatrics, Shinshu University School of Medicine.

出版信息

Rinsho Ketsueki. 2019;60(9):1351-1357. doi: 10.11406/rinketsu.60.1351.

Abstract

The adoptive transfer of chimeric antigen receptor (CAR)-modified autologous T cells targeted at the B-cell antigen CD19 is highly effective in patients with relapsed or refractory B-cell malignancies. In Japan, tisagenlecleucel has been approved in March 2019, whereas axicabtagene ciloleucel, lisocabtagene maraleucel, and TBI-1501 have been tested in clinical trials. In addition, allogeneic CD19 CAR T cells from family or third-party donors have been developed for treating B-cell malignancies. Moreover, CAR T-cell therapies for acute myeloid leukemia (AML), T-cell leukemia, and multiple myeloma are still under development. Our group is currently preparing a phase I study on granulocyte macrophage colony-stimulating factor receptor-targeted CAR T cells in pediatric and adult patients with AML.

摘要

靶向B细胞抗原CD19的嵌合抗原受体(CAR)修饰的自体T细胞过继性转移,对于复发或难治性B细胞恶性肿瘤患者具有很高的疗效。在日本,tisagenlecleucel于2019年3月获得批准,而axi-cabtagene ciloleucel、lisocabtagene maraleucel和TBI-1501已在临床试验中进行了测试。此外,已开发出来自家族或第三方供体的同种异体CD19 CAR T细胞用于治疗B细胞恶性肿瘤。而且,针对急性髓系白血病(AML)、T细胞白血病和多发性骨髓瘤的CAR T细胞疗法仍在研发中。我们团队目前正在准备一项针对AML儿童和成年患者的、靶向粒细胞巨噬细胞集落刺激因子受体的CAR T细胞的I期研究。

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