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嵌合抗原受体修饰 T 细胞治疗实体瘤的前景。

Prospects for chimeric antigen receptor-modified T cell therapy for solid tumors.

机构信息

The Engineering Research Center of Peptide Drug Discovery and Development, China Pharmaceutical University, Nanjing, Jiangsu, 210009, People's Republic of China.

State Key Laboratory of Natural Medicines, Ministry of Education, China Pharmaceutical University, Nanjing, Jiangsu, 210009, People's Republic of China.

出版信息

Mol Cancer. 2018 Jan 12;17(1):7. doi: 10.1186/s12943-018-0759-3.

Abstract

The potential for adoptive cell immunotherapy as a treatment against cancers has been demonstrated by the remarkable response in some patients with hematological malignancies using autologous T cells endowed with chimeric antigen receptors (CARs) specific for CD19. Clinical efficacy of CAR-T cell therapy for the treatment of solid tumors, however, is rare due to physical and biochemical factors. This review focuses on different aspects of multiple mechanisms of immunosuppression in solid tumors. We characterize the current state of CAR-modified T cell therapy and summarize the various strategies to combat the immunosuppressive microenvironment of solid tumors, with the aim of promoting T cell cytotoxicity and enhancing tumor cell eradication.

摘要

过继细胞免疫疗法作为一种治疗癌症的方法的潜力已经通过一些血液恶性肿瘤患者使用嵌合抗原受体 (CAR) 赋予自体 T 细胞对 CD19 的显著反应得到证实。然而,由于物理和生化因素,CAR-T 细胞疗法治疗实体瘤的临床疗效很少见。本综述重点介绍了实体瘤中多种免疫抑制机制的不同方面。我们描述了 CAR 修饰的 T 细胞治疗的现状,并总结了各种策略来对抗实体瘤的免疫抑制微环境,旨在促进 T 细胞的细胞毒性并增强肿瘤细胞的清除。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3509/5767005/3cbdf15fee3c/12943_2018_759_Fig1_HTML.jpg

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