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嵌合抗原受体 T 细胞疗法治疗胶质母细胞瘤的现状和进展。

Present Status and Advances in Chimeric Antigen Receptor T Cell Therapy for Glioblastoma.

机构信息

Henan Key Laboratory of Brain Targeted Bio-Nanomedicine, School of Life Sciences & School of Pharmacy, Henan University, 475004 Kaifeng, Henan, China.

Henan-Macquarie University Joint Centre for Biomedical Innovation, School of Life Sciences, Henan University, 475004 Kaifeng, Henan, China.

出版信息

Front Biosci (Landmark Ed). 2023 Sep 15;28(9):206. doi: 10.31083/j.fbl2809206.


DOI:10.31083/j.fbl2809206
PMID:37796692
Abstract

Adoptive chimeric antigen receptor (CAR) T cells designed to recognize specific tumor antigens have shown promising results in cancer therapy. While CAR T cell therapy has demonstrated notable clinical effectiveness for hematologic disease, efforts to develop therapies for solid tumors, including glioblastoma (GBM), have been hampered by heterogeneity, an immunosuppressive tumor microenvironment, and difficulty in trafficking. Several specific tumor antigens, such as IL13Rα2, EGFRvIII, and HER2, have been attempted in clinical trials; however, limited efficacy has been observed. In this review, we discuss the current status of CAR T therapy for GBM in clinical trials and highlight the potential target antigens for CAR T cells. Additionally, we summarize the mechanisms used to enhance their efficacy and explore the challenges and future prospects of CAR T cell therapy for GBM.

摘要

嵌合抗原受体 (CAR) T 细胞是为识别特定肿瘤抗原而设计的,在癌症治疗中显示出了有前景的结果。虽然 CAR T 细胞疗法已在血液疾病的治疗中显示出显著的临床疗效,但针对实体瘤(包括胶质母细胞瘤 [GBM])的治疗方法的发展却受到了异质性、免疫抑制性肿瘤微环境以及运输困难的阻碍。在临床试验中尝试了几种特定的肿瘤抗原,如 IL13Rα2、EGFRvIII 和 HER2,但观察到疗效有限。在这篇综述中,我们讨论了 CAR T 疗法在 GBM 临床试验中的现状,并强调了 CAR T 细胞的潜在靶抗原。此外,我们总结了用于增强其疗效的机制,并探讨了 CAR T 细胞治疗 GBM 的挑战和未来前景。

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[3]
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[5]
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引用本文的文献

[1]
Cytokine Modification of Adoptive Chimeric Antigen Receptor Immunotherapy for Glioblastoma.

Cancers (Basel). 2023-12-15

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