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基于嵌合抗原受体T细胞的癌症免疫疗法

Chimeric Antigen Receptor T Cell Based Immunotherapy for Cancer.

作者信息

Li Feng, Zhang Tengfei, Cao Ling, Zhang Yi

机构信息

Biotherapy Center, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.

Department of Hematology and Oncology, Harvard Medical School, Boston, MA, United States.

出版信息

Curr Stem Cell Res Ther. 2018;13(5):327-335. doi: 10.2174/1574888X13666180420110239.

Abstract

Cancer immunotherapy, a new weapon against cancers by harnessing the patient's own immune system, potentiates an extended remission and possibly a cure for cancer. T cells genetically engineered with chimeric antigen receptor (CAR) vectors can specifically target the surface antigen of cancer cells and kill them in an MHC-independent manner. CD19 is extensively expressed on cancerous cells in B cell malignancies. To target this antigen, CAR T cells have gained great success in treating patients with B cell leukemia and lymphoma. Currently, the data from clinical trials on CAR T cells in solid tumors are limited; thus, CAR T cells targeting GD2, HER2, EGFRvIII, CSPG4, DNAX, mesothelin, and other molecules are under active investigation for solid tumors. In this review, we summarize the clinical results for CAR T cells in the case of hematologic and solid tumors, along with the current developments in CAR T cell immunotherapy.

摘要

癌症免疫疗法是通过利用患者自身免疫系统对抗癌症的一种新武器,可延长缓解期并有可能治愈癌症。用嵌合抗原受体(CAR)载体进行基因工程改造的T细胞能够特异性靶向癌细胞表面抗原,并以不依赖主要组织相容性复合体(MHC)的方式将其杀死。CD19在B细胞恶性肿瘤的癌细胞上广泛表达。为了靶向这种抗原,CAR-T细胞在治疗B细胞白血病和淋巴瘤患者方面取得了巨大成功。目前,针对实体瘤的CAR-T细胞临床试验数据有限;因此,靶向GD2、HER2、表皮生长因子受体III型变异体(EGFRvIII)、硫酸软骨素蛋白聚糖4(CSPG4)、DNAX、间皮素和其他分子的CAR-T细胞正在针对实体瘤进行积极研究。在这篇综述中,我们总结了CAR-T细胞在血液系统肿瘤和实体瘤病例中的临床结果,以及CAR-T细胞免疫疗法的当前进展。

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