T-cell receptor-engineered T cells for cancer treatment: current status and future directions

被引:109
|
作者
Ping, Yu [1 ]
Liu, Chaojun [1 ]
Zhang, Yi [1 ,2 ,3 ]
机构
[1] Zhengzhou Univ, Affiliated Hosp 1, Biotherapy Ctr, Zhengzhou 450052, Henan, Peoples R China
[2] Zhengzhou Univ, Affiliated Hosp 1, Canc Ctr, Zhengzhou 450052, Henan, Peoples R China
[3] Engn Key Lab Cell Therapy Henan Prov, Zhengzhou 450052, Henan, Peoples R China
基金
中国国家自然科学基金;
关键词
T-cell receptor; tumor antigen; TCR-engineered T cells; neoantigen; tumor microenvironment; TUMOR-INFILTRATING LYMPHOCYTES; CHIMERIC ANTIGEN RECEPTOR; EXOME ANALYSIS REVEALS; METASTATIC MELANOMA; ADOPTIVE TRANSFER; IN-VIVO; EPITHELIAL CANCER; CTLA-4; BLOCKADE; PD-1; GENE-THERAPY;
D O I
10.1007/s13238-016-0367-1
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
T-cell receptor (TCR)-engineered T cells are a novel option for adoptive cell therapy used for the treatment of several advanced forms of cancer. Work using TCR-engineered T cells began more than two decades ago, with numerous preclinical studies showing that such cells could mediate tumor lysis and eradication. The success of these trials provided the foundation for clinical trials, including recent clinical successes using TCR-engineered T cells to target New York esophageal squamous cell carcinoma (NY-ESO-1). These successes demonstrate the potential of this approach to treat cancer. In this review, we provide a perspective on the current and future applications of TCR-engineered T cells for the treatment of cancer. Our summary focuses on TCR activation and both pre-clinical and clinical applications of TCR-engineered T cells. We also discuss how to enhance the function of TCR-engineered T cells and prolong their longevity in the tumor microenvironment.
引用
收藏
页码:254 / 266
页数:13
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