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T细胞接合免疫疗法,重点介绍嵌合抗原受体(CAR)T细胞疗法。

T Cell Engaging Immunotherapies, Highlighting Chimeric Antigen Receptor (CAR) T Cell Therapy.

作者信息

De Bousser Elien, Callewaert Nico, Festjens Nele

机构信息

Vlaams Instituut voor Biotechnologie (VIB)-UGent Center for Medical Biotechnology, Technologiepark-Zwijnaarde 75, 9052 Ghent, Belgium.

Department of Biochemistry and Microbiology, Ghent University, Technologiepark-Zwijnaarde 75, 9052 Ghent, Belgium.

出版信息

Cancers (Basel). 2021 Dec 1;13(23):6067. doi: 10.3390/cancers13236067.

Abstract

In the past decade, chimeric antigen receptor (CAR) T cell technology has revolutionized cancer immunotherapy. This strategy uses synthetic CARs to redirect the patient's own immune cells to recognize specific antigens expressed on the surface of tumor cells. The unprecedented success of anti-CD19 CAR T cell therapy against B cell malignancies has resulted in its approval by the US Food and Drug Administration (FDA) in 2017. However, major scientific challenges still remain to be addressed for the broad use of CAR T cell therapy. These include severe toxicities, limited efficacy against solid tumors, and immune suppression in the hostile tumor microenvironment. Furthermore, CAR T cell therapy is a personalized medicine of which the production is time- and resource-intensive, which makes it very expensive. All these factors drive new innovations to engineer more powerful CAR T cells with improved antitumor activity, which are reviewed in this manuscript.

摘要

在过去十年中,嵌合抗原受体(CAR)T细胞技术彻底改变了癌症免疫疗法。该策略使用合成的CAR来重定向患者自身的免疫细胞,以识别肿瘤细胞表面表达的特定抗原。抗CD19 CAR T细胞疗法针对B细胞恶性肿瘤取得了前所未有的成功,导致其于2017年获得美国食品药品监督管理局(FDA)的批准。然而,CAR T细胞疗法的广泛应用仍面临重大科学挑战。这些挑战包括严重的毒性、对实体瘤的疗效有限以及在恶劣肿瘤微环境中的免疫抑制。此外,CAR T细胞疗法是一种个性化药物,其生产需要大量时间和资源,这使其成本非常高昂。所有这些因素推动了新的创新,以设计出具有更强抗肿瘤活性的更强大的CAR T细胞,本文将对此进行综述。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c13/8657024/6f33680bbe97/cancers-13-06067-g001.jpg

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