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用于脑胶质瘤嵌合抗原受体 T 细胞治疗的临床前模型。

Pre-Clinical Models for CAR T-Cell Therapy for Glioma.

机构信息

Brain Tumor Immunotherapy Lab, Department of Neurosurgery, Massachusetts General Hospital, Harvard Medical School, Boston, MA 02114, USA.

Faculty of Medicine, KU Leuven, 3000 Leuven, Belgium.

出版信息

Cells. 2024 Sep 4;13(17):1480. doi: 10.3390/cells13171480.

DOI:10.3390/cells13171480
PMID:39273050
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11394304/
Abstract

Immunotherapy represents a transformative shift in cancer treatment. Among myriad immune-based approaches, chimeric antigen receptor (CAR) T-cell therapy has shown promising results in treating hematological malignancies. Despite aggressive treatment options, the prognosis for patients with malignant brain tumors remains poor. Research leveraging CAR T-cell therapy for brain tumors has surged in recent years. Pre-clinical models are crucial in evaluating the safety and efficacy of these therapies before they advance to clinical trials. However, current models recapitulate the human tumor environment to varying degrees. Novel in vitro and in vivo techniques offer the opportunity to validate CAR T-cell therapies but also have limitations. By evaluating the strengths and weaknesses of various pre-clinical glioma models, this review aims to provide a roadmap for the development and pre-clinical testing of CAR T-cell therapies for brain tumors.

摘要

免疫疗法代表了癌症治疗的重大转变。在众多基于免疫的方法中,嵌合抗原受体 (CAR) T 细胞疗法在治疗血液系统恶性肿瘤方面显示出了有前景的结果。尽管有积极的治疗选择,患有恶性脑肿瘤的患者的预后仍然很差。近年来,利用 CAR T 细胞疗法治疗脑肿瘤的研究激增。临床前模型在这些疗法进入临床试验之前,对于评估其安全性和有效性至关重要。然而,目前的模型在不同程度上再现了人类肿瘤环境。新型的体外和体内技术为验证 CAR T 细胞疗法提供了机会,但也存在局限性。通过评估各种临床前神经胶质瘤模型的优缺点,本综述旨在为脑肿瘤的 CAR T 细胞疗法的开发和临床前测试提供一个路线图。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/969b/11394304/c4704a272518/cells-13-01480-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/969b/11394304/f01c5109b530/cells-13-01480-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/969b/11394304/c4704a272518/cells-13-01480-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/969b/11394304/f01c5109b530/cells-13-01480-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/969b/11394304/c4704a272518/cells-13-01480-g002.jpg

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2
CAR T cells offer hope in glioblastoma.嵌合抗原受体T细胞为胶质母细胞瘤带来了希望。
Nat Rev Neurol. 2024 Jun;20(6):315. doi: 10.1038/s41582-024-00972-w.
3
Lifileucel: First Approval.利利昔单抗:首次批准。
Mol Diagn Ther. 2024 May;28(3):339-344. doi: 10.1007/s40291-024-00708-y. Epub 2024 Apr 16.
4
CD19 CAR-expressing iPSC-derived NK cells effectively enhance migration and cytotoxicity into glioblastoma by targeting to the pericytes in tumor microenvironment.CD19 CAR 表达的 iPSC 衍生 NK 细胞通过靶向肿瘤微环境中的周细胞,有效增强了对神经胶质瘤的迁移和细胞毒性。
Biomed Pharmacother. 2024 May;174:116436. doi: 10.1016/j.biopha.2024.116436. Epub 2024 Mar 19.
5
Intraventricular CARv3-TEAM-E T Cells in Recurrent Glioblastoma.脑室 CARv3-TEAM-E 细胞治疗复发性脑胶质瘤。
N Engl J Med. 2024 Apr 11;390(14):1290-1298. doi: 10.1056/NEJMoa2314390. Epub 2024 Mar 13.
6
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7
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8
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9
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Cancer Res Commun. 2023 Dec 1;3(12):2430-2446. doi: 10.1158/2767-9764.CRC-23-0424.