TCR-engineered T cell therapy in solid tumors: State of the art and perspectives

被引:212
作者
Baulu, Estelle [1 ,2 ]
Gardet, Celia [1 ]
Chuvin, Nicolas [2 ]
Depil, Stephane [1 ,2 ,3 ,4 ]
机构
[1] Ctr Rech Cancerol Lyon, Lyon, France
[2] ErVaccine Technol, Lyon, France
[3] Ctr Leon Berard, Lyon, France
[4] Univ Claude Bernard Lyon 1, Lyon, France
关键词
ENHANCED ANTITUMOR-ACTIVITY; CANCER REGRESSION; CROSS-REACTIVITY; ADOPTIVE TRANSFER; GENE-THERAPY; RECEPTOR; LYMPHOCYTES; AFFINITY; IMMUNOTHERAPY; ANTIGENS;
D O I
10.1126/sciadv.adf3700
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
T cell engineering has changed the landscape of cancer immunotherapy. Chimeric antigen receptor T cells have demonstrated a remarkable efficacy in the treatment of B cell malignancies in hematology. However, their clinical impact on solid tumors has been modest so far. T cells expressing an engineered T cell receptor (TCR-T cells) represent a promising therapeutic alternative. The target repertoire is not limited to membrane proteins, and intrinsic features of TCRs such as high antigen sensitivity and near-to-physiological signaling may improve tumor cell detection and killing while improving T cell persistence. In this review, we present the clinical results obtained with TCR-T cells targeting different tumor antigen families. We detail the different methods that have been developed to identify and optimize a TCR candidate. We also discuss the challenges of TCR-T cell therapies, including toxicity assessment and resistance mechanisms. Last, we share some perspectives and highlight future directions in the field.
引用
收藏
页数:16
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