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2
Current progress in chimeric antigen receptor T cell therapy for glioblastoma multiforme.嵌合抗原受体 T 细胞疗法治疗多形性胶质母细胞瘤的研究进展。
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本文引用的文献

1
Emerging Approaches for Regulation and Control of CAR T Cells: A Mini Review.新兴的 CAR T 细胞调控方法:综述
Front Immunol. 2020 Feb 26;11:326. doi: 10.3389/fimmu.2020.00326. eCollection 2020.
2
CAR-T cells secreting BiTEs circumvent antigen escape without detectable toxicity.分泌双特异性 T 细胞衔接子(BiTEs)的 CAR-T 细胞可规避抗原逃逸而无明显毒性。
Nat Biotechnol. 2019 Sep;37(9):1049-1058. doi: 10.1038/s41587-019-0192-1. Epub 2019 Jul 22.
3
An Integrative Model of Cellular States, Plasticity, and Genetics for Glioblastoma.胶质母细胞瘤的细胞状态、可塑性和遗传学综合模型
Cell. 2019 Aug 8;178(4):835-849.e21. doi: 10.1016/j.cell.2019.06.024. Epub 2019 Jul 18.
4
Multilayered Heterogeneity of Glioblastoma Stem Cells: Biological and Clinical Significance.胶质母细胞瘤干细胞的多层次异质性:生物学和临床意义。
Adv Exp Med Biol. 2019;1139:1-21. doi: 10.1007/978-3-030-14366-4_1.
5
Pilot Trial of Adoptive Transfer of Chimeric Antigen Receptor-transduced T Cells Targeting EGFRvIII in Patients With Glioblastoma.嵌合抗原受体修饰的 T 细胞过继转移治疗胶质母细胞瘤患者中针对 EGFRvIII 的初步临床试验
J Immunother. 2019 May;42(4):126-135. doi: 10.1097/CJI.0000000000000260.
6
Immunotherapy for Glioblastoma: Adoptive T-cell Strategies.胶质母细胞瘤的免疫治疗:过继性 T 细胞策略。
Clin Cancer Res. 2019 Apr 1;25(7):2042-2048. doi: 10.1158/1078-0432.CCR-18-1625. Epub 2018 Nov 16.
7
Clinical and Biological Correlates of Neurotoxicity Associated with CAR T-cell Therapy in Patients with B-cell Acute Lymphoblastic Leukemia.与 B 细胞急性淋巴细胞白血病患者的 CAR T 细胞治疗相关的神经毒性的临床和生物学相关性。
Cancer Discov. 2018 Aug;8(8):958-971. doi: 10.1158/2159-8290.CD-17-1319. Epub 2018 Jun 7.
8
Insights into cytokine release syndrome and neurotoxicity after CD19-specific CAR-T cell therapy.细胞因子释放综合征和神经毒性的新见解:CD19 特异性嵌合抗原受体 T 细胞治疗后。
Curr Res Transl Med. 2018 May;66(2):50-52. doi: 10.1016/j.retram.2018.03.003. Epub 2018 Apr 3.
9
Immune evasion mediated by PD-L1 on glioblastoma-derived extracellular vesicles.由胶质母细胞瘤衍生的细胞外囊泡上的 PD-L1 介导的免疫逃逸。
Sci Adv. 2018 Mar 7;4(3):eaar2766. doi: 10.1126/sciadv.aar2766. eCollection 2018 Mar.
10
CAR T-cell therapy for glioblastoma: recent clinical advances and future challenges.嵌合抗原受体 T 细胞疗法治疗胶质母细胞瘤:最新临床进展与未来挑战。
Neuro Oncol. 2018 Oct 9;20(11):1429-1438. doi: 10.1093/neuonc/noy032.

嵌合抗原受体 T 细胞疗法:胶质母细胞瘤治疗的新进展。

Chimeric Antigen Receptor T-Cell Therapy: Updates in Glioblastoma Treatment.

机构信息

Division of Neurosurgery, City of Hope National Medical Center, Duarte, California.

Department of Cancer Immunotherapy & Tumor Immunology, City of Hope National Medical Center, Duarte, California.

出版信息

Neurosurgery. 2021 May 13;88(6):1056-1064. doi: 10.1093/neuros/nyaa584.

DOI:10.1093/neuros/nyaa584
PMID:33575786
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8324243/
Abstract

Glioblastoma multiforme (GBM) are the most common and among the deadliest brain tumors in adults. Current mainstay treatments are insufficient to treat this tumor, and therefore, more effective therapies are desperately needed. Immunotherapy, which takes advantage of the body's natural defense mechanism, is an exciting emerging field in neuro-oncology. Adoptive cell therapy with chimeric antigen receptor (CAR) T cells provides a treatment strategy based on using patients' own selected and genetically engineered cells that target tumor-associated antigens. These cells are harvested from patients, modified to target specific proteins expressed by the tumor, and re-introduced into the patient with the goal of destroying tumor cells. Here, we review the history of CAR T-cell therapy, and describe the characteristics of various generations of CAR T therapies, and the challenges inherent to treatment of GBM. Finally, we describe recent and current CAR T clinical trials designed to combat GBM.

摘要

胶质母细胞瘤(GBM)是成人中最常见且最致命的脑肿瘤之一。目前的主要治疗方法不足以治疗这种肿瘤,因此迫切需要更有效的治疗方法。免疫疗法利用了人体的自然防御机制,是神经肿瘤学中一个令人兴奋的新兴领域。嵌合抗原受体(CAR)T 细胞的过继细胞疗法提供了一种基于利用患者自身选择和基因工程细胞的治疗策略,这些细胞靶向肿瘤相关抗原。这些细胞从患者中采集,经过修饰以靶向肿瘤表达的特定蛋白质,然后重新引入患者体内,以破坏肿瘤细胞。在这里,我们回顾了 CAR T 细胞疗法的历史,描述了各种代 CAR T 疗法的特点,以及治疗 GBM 所固有的挑战。最后,我们描述了最近和目前旨在对抗 GBM 的 CAR T 临床试验。