Chimeric antigen receptor T cells: a novel therapy for solid tumors

被引:207
|
作者
Yu, Shengnan [1 ]
Li, Anping [2 ]
Liu, Qian [1 ]
Li, Tengfei [2 ]
Yuan, Xun [1 ]
Han, Xinwei [2 ]
Wu, Kongming [1 ]
机构
[1] Zhengzhou Univ, Dept Intervent Radiol, Affiliated Hosp 1, Zhengzhou 450052, Peoples R China
[2] Huazhong Univ Sci & Technol, Tongji Hosp, Dept Oncol, Tongji Med Coll, Wuhan 430030, Peoples R China
来源
JOURNAL OF HEMATOLOGY & ONCOLOGY | 2017年 / 10卷
基金
国家高技术研究发展计划(863计划); 中国国家自然科学基金;
关键词
CAR-T cell; EGFR; HER2; Mesothelin; Solid tumors; GROWTH-FACTOR RECEPTOR; MALIGNANT PLEURAL MESOTHELIOMA; I CLINICAL-TRIAL; ANTITUMOR-ACTIVITY; CANCER-IMMUNOTHERAPY; STEM-CELLS; ADOPTIVE TRANSFER; SERUM MESOTHELIN; PROSTATE-CANCER; BREAST-CANCER;
D O I
10.1186/s13045-017-0444-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The chimeric antigen receptor T (CAR-T) cell therapy is a newly developed adoptive antitumor treatment. Theoretically, CAR-T cells can specifically localize and eliminate tumor cells by interacting with the tumor-associated antigens (TAAs) expressing on tumor cell surface. Current studies demonstrated that various TAAs could act as target antigens for CAR-T cells, for instance, the type III variant epidermal growth factor receptor (EGFRvIII) was considered as an ideal target for its aberrant expression on the cell surface of several tumor types. CAR-T cell therapy has achieved gratifying breakthrough in hematological malignancies and promising outcome in solid tumor as showed in various clinical trials. The third generation of CAR-T demonstrates increased antitumor cytotoxicity and persistence through modification of CAR structure. In this review, we summarized the preclinical and clinical progress of CAR-T cells targeting EGFR, human epidermal growth factor receptor 2 (HER2), and mesothelin (MSLN), as well as the challenges for CAR-T cell therapy.
引用
收藏
页数:13
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