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中枢神经系统肿瘤的嵌合抗原受体T细胞(CAR-T)疗法进展

Advances in CAR-T therapy for central nervous system tumors.

作者信息

Zhou Delian, Zhu Xiaojian, Xiao Yi

机构信息

Department of Hematology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, 430030, China.

出版信息

Biomark Res. 2024 Nov 6;12(1):132. doi: 10.1186/s40364-024-00679-6.

Abstract

The application of chimeric antigen receptor T-cell therapy in central nervous system tumors has significantly advanced; however, challenges pertaining to the blood-brain barrier, immunosuppressive microenvironment, and antigenic heterogeneity continue to be encountered, unlike its success in hematological malignancies such as acute lymphoblastic leukemia and diffuse large B-cell lymphomas. This review examined the research progress of chimeric antigen receptor T-cell therapy in gliomas, medulloblastomas, and lymphohematopoietic tumors of the central nervous system, focusing on chimeric antigen receptor T-cells targeting antigens such as EGFRvIII, HER2, B7H3, GD2, and CD19 in preclinical and clinical studies. It synthesized current research findings to offer valuable insights for future chimeric antigen receptor T-cell therapeutic strategies for central nervous system tumors and advance the development and application of this therapeutic modality in this domain.

摘要

嵌合抗原受体T细胞疗法在中枢神经系统肿瘤中的应用取得了显著进展;然而,与它在急性淋巴细胞白血病和弥漫性大B细胞淋巴瘤等血液系统恶性肿瘤中的成功不同,在血脑屏障、免疫抑制微环境和抗原异质性方面仍然面临挑战。本综述研究了嵌合抗原受体T细胞疗法在神经胶质瘤、髓母细胞瘤和中枢神经系统淋巴造血肿瘤中的研究进展,重点关注临床前和临床研究中针对表皮生长因子受体III型变异体(EGFRvIII)、人表皮生长因子受体2(HER2)、B7同源蛋白3(B7H3)、二唾液酸神经节苷脂(GD2)和CD19等抗原的嵌合抗原受体T细胞。它综合了当前的研究结果,为未来中枢神经系统肿瘤的嵌合抗原受体T细胞治疗策略提供有价值的见解,并推动这种治疗方式在该领域的开发和应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4188/11539471/e261ec3ddc85/40364_2024_679_Fig1_HTML.jpg

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