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CAR-T 细胞治疗急性髓系白血病的最新进展

英文原题:Recent advances in CAR-T cell therapy for acute myeloid leukaemia.

查看英文原题

Recent advances in CAR-T cell therapy for acute myeloid leukaemia.

PubMed 2024/05/01(内容时间) J Cell Mol Med Q2 · IF 4.7(JCR 2025)

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中文摘要

急性髓系白血病(AML)是一种致命且难治的血液癌症,主要影响成人,并干扰骨髓细胞增殖。尽管已有化疗、异基因造血干细胞移植(allo-HSCT)和受体拮抗剂等治疗,患者 5 年生存率仍低于 30%。Allo-HSCT 是 AML 治疗的主要方法,但存在移植物抗宿主病(GVHD)等严重副作用。近年来,嵌合抗原受体(CAR)T 细胞疗法在癌症治疗中取得显著进展。这些工程化 T 细胞可在体内定位并识别肿瘤细胞,通过免疫作用释放大量效应分子,有效杀伤肿瘤细胞,因此成为最有效的癌症治疗方法之一。多项临床研究显示 CAR-T 治疗 AML 取得积极疗效。本综述重点介绍 AML 免疫治疗新靶点的近期进展,以及 CAR-T 治疗 AML 的局限和难题。

展开英文摘要原文

Acute myeloid leukaemia (AML) is a fatal and refractory haematologic cancer that primarily affects adults. It interferes with bone marrow cell proliferation. Patients have a 5 years survival rate of less than 30% despite the availability of several treatments, including chemotherapy, allogeneic haematopoietic stem cell transplantation (Allo-HSCT), and receptor antagonist drugs. Allo-HSCT is the mainstay of acute myeloid leukaemia treatment. Although it does work, there are severe side effects, such as graft-versus-host disease (GVHD). In recent years, chimeric antigen receptor (CAR)-T cell therapies have made significant progress in the treatment of cancer.

These engineered T cells can locate and recognize tumour cells in vivo and release a large number of effectors through immune action to effectively kill tumour cells. CAR-T cells are among the most effective cancer treatments because of this property. CAR-T cells have demonstrated positive therapeutic results in the treatment of acute myeloid leukaemia, according to numerous clinical investigations. This review highlights recent progress in new targets for AML immunotherapy, and the limitations, and difficulties of CAR-T therapy for AML.

论文信息

作者
Gao C、Li X、Xu Y、Zhang T、Zhu H、Yao D
单位
College of Life Science and Health, Wuhan University of Science and Technology, Wuhan, China.China
文献类型
综述 · 非美国政府资助研究
期刊
Journal of cellular and molecular medicine2024 May
原文标识
PubMed 38712978 · DOI 10.1111/jcmm.18369