Chimeric Antigen Receptors Modified T-Cells for Cancer Therapy

被引:252
作者
Dai, Hanren [1 ,3 ]
Wang, Yao [1 ,3 ]
Lu, Xuechun [4 ]
Han, Weidong [1 ,2 ,3 ]
机构
[1] Chinese Peoples Liberat Army Gen Hosp, Sch Life Sci, Inst Basic Med, Dept Immunol, Beijing 100853, Peoples R China
[2] Chinese Peoples Liberat Army Gen Hosp, Sch Life Sci, Inst Basic Med, Dept Mol Biol, Beijing 100853, Peoples R China
[3] Chinese Peoples Liberat Army Gen Hosp, Dept Biotherapeut, Beijing 100853, Peoples R China
[4] Chinese Peoples Liberat Army Gen Hosp, Dept Hematol, Beijing 100853, Peoples R China
来源
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE | 2016年 / 108卷 / 07期
基金
中国国家自然科学基金;
关键词
IN-VIVO PERSISTENCE; ADOPTIVE IMMUNOTHERAPY; ANTITUMOR-ACTIVITY; GENETIC-MODIFICATION; SUICIDE-GENE; DONOR LYMPHOCYTES; TUMOR-CELLS; PHASE-I; CYTOKINE RELEASE; CLINICAL-TRIAL;
D O I
10.1093/jnci/djv439
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
The genetic modification and characterization of T-cells with chimeric antigen receptors (CARs) allow functionally distinct T-cell subsets to recognize specific tumor cells. The incorporation of costimulatory molecules or cytokines can enable engineered T-cells to eliminate tumor cells. CARs are generated by fusing the antigen-binding region of a monoclonal antibody (mAb) or other ligand to membrane-spanning and intracellular-signaling domains. They have recently shown clinical benefit in patients treated with CD19-directed autologous T-cells. Recent successes suggest that the modification of T-cells with CARs could be a powerful approach for developing safe and effective cancer therapeutics. Here, we briefly review early studies, consider strategies to improve the therapeutic potential and safety, and discuss the challenges and future prospects for CAR T-cells in cancer therapy.
引用
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页数:14
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