Cancer Therapy With TCR-Engineered T Cells: Current Strategies, Challenges, and Prospects

被引:88
|
作者
Shafer, Paul [1 ,2 ,3 ,4 ]
Kelly, Lauren M. [1 ,2 ,3 ,5 ]
Hoyos, Valentina [1 ,2 ,3 ]
机构
[1] Baylor Coll Med, Texas Childrens Hosp, Ctr Cell & Gene Therapy, Houston, TX 77030 USA
[2] Houston Methodist Hosp, Houston, TX 77030 USA
[3] Baylor Coll Med, Dan L Duncan Canc Ctr, Houston, TX 77030 USA
[4] Baylor Coll Med, Program Immunol, Houston, TX 77030 USA
[5] Baylor Coll Med, Program Canc & Cell Biol, Houston, TX 77030 USA
来源
FRONTIERS IN IMMUNOLOGY | 2022年 / 13卷
基金
美国国家卫生研究院;
关键词
T cell receptor; TCR; chimeric antigen receptor; CAR; TCR-engineered T cells; TCR T; adoptive cell therapy; TUMOR-INFILTRATING LYMPHOCYTES; CHIMERIC ANTIGEN RECEPTOR; EPSTEIN-BARR-VIRUS; GENE-TRANSDUCED LYMPHOCYTES; ENHANCED ANTITUMOR-ACTIVITY; GREEN FLUORESCENT PROTEIN; IN-VITRO STIMULATION; VERSUS-HOST-DISEASE; SINGLE-CHAIN; METASTATIC MELANOMA;
D O I
10.3389/fimmu.2022.835762
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
To redirect T cells against tumor cells, T cells can be engineered ex vivo to express cancer-antigen specific T cell receptors (TCRs), generating products known as TCR-engineered T cells (TCR T). Unlike chimeric antigen receptors (CARs), TCRs recognize HLA-presented peptides derived from proteins of all cellular compartments. The use of TCR T cells for adoptive cellular therapies (ACT) has gained increased attention, especially as efforts to treat solid cancers with ACTs have intensified. In this review, we describe the differing mechanisms of T cell antigen recognition and signal transduction mediated through CARs and TCRs. We describe the classes of cancer antigens recognized by current TCR T therapies and discuss both classical and emerging pre-clinical strategies for antigen-specific TCR discovery, enhancement, and validation. Finally, we review the current landscape of clinical trials for TCR T therapy and discuss what these current results indicate for the development of future engineered TCR approaches.
引用
收藏
页数:24
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