Empirical and Rational Design of T Cell Receptor-Based Immunotherapies

被引:21
作者
Jones, Heather F. [1 ,2 ]
Molvi, Zaki [2 ,3 ]
Klatt, Martin G. [1 ]
Dao, Tao [1 ]
Scheinberg, David A. [1 ,2 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Mol Pharmacol Program, 1275 York Ave, New York, NY 10021 USA
[2] Weill Cornell Med, New York, NY 10065 USA
[3] Mem Sloan Kettering Canc Ctr, Immunol Program, 1275 York Ave, New York, NY 10021 USA
来源
FRONTIERS IN IMMUNOLOGY | 2021年 / 11卷
关键词
T cell receptor; bispecific T cell engager; cross-reactivity; tumor infiltrating lymphocytes; immune mobilizing monoclonal T cell receptors against cancer; peptide; major histocompatibility complexes; T cell receptor mimic monoclonal antibody; T cell receptor-T cell;
D O I
10.3389/fimmu.2020.585385
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The use of T cells reactive with intracellular tumor-associated or tumor-specific antigens has been a promising strategy for cancer immunotherapies in the past three decades, but the approach has been constrained by a limited understanding of the T cell receptor's (TCR) complex functions and specificities. Newer TCR and T cell-based approaches are in development, including engineered adoptive T cells with enhanced TCR affinities, TCR mimic antibodies, and T cell-redirecting bispecific agents. These new therapeutic modalities are exciting opportunities by which TCR recognition can be further exploited for therapeutic benefit. In this review we summarize the development of TCR-based therapeutic strategies and focus on balancing efficacy and potency versus specificity, and hence, possible toxicity, of these powerful therapeutic modalities.
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页数:21
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