To affinity and beyond: Harnessing the T Cell receptor for cancer immunotherapy

被引:24
作者
Thaxton, Jessica E. [1 ]
Li, Zihai [1 ]
机构
[1] Med Univ S Carolina, Dept Microbiol & Immunol, Hollings Canc Ctr, Charleston, SC 29425 USA
关键词
affinity; adoptive cell therapy; cancer; co-receptor; T cell receptor; tumor; TCR; CDR; complementarity determining region; MHC; major histocompatibility complex; SLEC; short-lived effector cell; mTEC; medullary thymic epithelial cell; TSA; tissue-specific self-antigen; AIRE; autoimmune regulator; TIL; tumor infiltrating lymphocyte; TAA; tumor-associated antigen; CTA; cancer testis antigen; TUMOR-INFILTRATING LYMPHOCYTES; THYMOCYTE POSITIVE SELECTION; METASTATIC MELANOMA; DENDRITIC CELLS; GENE-THERAPY; NEGATIVE SELECTION; ANTIGEN RECEPTOR; IMMUNE-RESPONSES; EPITHELIAL-CELLS; CUTTING EDGE;
D O I
10.4161/21645515.2014.973314
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
T cell adoptive therapies for immune-mediated regression of cancers have attracted a great deal of recent attention. Clinical results are glamorous, yet much remains to be uncovered behind the basic science that allows us to engineer T cells and T cell receptors (TCRs) for clinical use. We discuss the development of TCRs for therapeutic use in the context of thymic selection toward central tolerance and we review therapies based on tumor infiltrating lymphocytes (TILs), endogenous antigen specific TCRs, and engineered TCRs. Further we discuss the development of low and high affinity TCRs and the extent to which each challenges central tolerance. Current results suggest that adaptation of TCR engineering of moderate affinity TCRs coupled with co-regulatory and stimulatory molecules may be the safest and most efficacious road for TCR development aimed at tumor abolition.
引用
收藏
页码:3313 / 3321
页数:9
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