TCR engineered T cells for solid tumor immunotherapy

被引:37
|
作者
Zhang, Yikai [1 ,2 ,3 ,4 ]
Liu, Zhipeng [1 ,2 ]
Wei, Wei [1 ,2 ]
Li, Yangqiu [3 ,4 ]
机构
[1] Guangzhou Municipal Tianhe Nuoya Bioengn Co Ltd, Guangzhou 510663, Peoples R China
[2] Guangdong Cord Blood Bank, Guangzhou 510663, Peoples R China
[3] Jinan Univ, Affiliated Hosp 1, Dept Hematol, Guangzhou 510632, Peoples R China
[4] Jinan Univ, Sch Med, Inst Hematol, Key Lab Regenerat Med,Minist Educ, 601 Huang Pu Dao Xi, Guangzhou 510632, Peoples R China
基金
中国博士后科学基金;
关键词
T cell receptor; TCR-T cells; Cellular immunotherapy; Solid tumors; RECEPTOR GENE-THERAPY; CANCER REGRESSION; ADOPTIVE TRANSFER; LYMPHOCYTES; MELANOMA; TRIAL; MICROENVIRONMENT; IDENTIFICATION; SPECIFICITY; RECOGNITION;
D O I
10.1186/s40164-022-00291-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
T cell immunotherapy remains an attractive approach for cancer immunotherapy. T cell immunotherapy mainly employs chimeric antigen receptor (CAR)- and T cell receptor (TCR)-engineered T cells. CAR-T cell therapy has been an essential breakthrough in treating hematological malignancies. TCR-T cells can recognize antigens expressed both on cell surfaces and in intracellular compartments. Although TCR-T cells have not been approved for clinical application, a number of clinical trials have been performed, particularly for solid tumors. In this article, we summarized current TCR-T cell advances and their potential advantages for solid tumor immunotherapy.
引用
收藏
页数:11
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