The Emergence of T-Bodies/CAR T Cells

被引:50
作者
Eshhar, Zelig [1 ,2 ]
Waks, Tova [1 ,2 ]
Gross, Gideon [3 ,4 ]
机构
[1] Weizmann Inst Sci, Dept Immunol, IL-76100 Rehovot, Israel
[2] Tel Aviv Univ, Tel Aviv Sourasky Med Ctr, Immunol Res Ctr, IL-69978 Tel Aviv, Israel
[3] Galilee Res Inst, MIGAL, Kiryat Shmona, Israel
[4] Tel Hai Coll, Upper Galilee, Israel
关键词
Chimeric receptors; CAR; T-bodies; cancer immunotherapy; cell and gene engineering; CHIMERIC-ANTIGEN-RECEPTOR; SINGLE-CHAIN; ANTITUMOR-ACTIVITY; ADOPTIVE IMMUNOTHERAPY; FUNCTIONAL RECEPTORS; SIGNALING DOMAINS; OPTIMAL-DESIGN; STEM-CELLS; ZETA-CHAIN; CANCER;
D O I
10.1097/PPO.0000000000000027
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The nickname "T-body" is used to denote a T cell expressing an antigen-specific or antibody-based chimeric receptor that combines antibody specificity with T-cell effector or regulatory function. Initially, we designed and constructed chimeric antibody-based receptors and expressed them in T cells to study the role of major histocompatibility complex in triggering T-cell activation. To this end, we replaced both variable domains (V alpha and V beta of the native T-cell receptor chains) with antibody-derived V-H and V-L sequences. After transfection into T cells, the 2 chimeric chains paired, associated with the CD3 complex, and endowed transfectants with non-major histocompatibility complex-restricted antibody type specificity. In subsequent studies, we developed next generation of chimeric antibody-based receptors by fusing an antibody single-chain variable fragment to T-cell activation motifs. This modular configuration simplified gene transfer, avoided mixed pairing with endogenous T-cell receptor chains, and enabled simultaneous insertion of various domains as costimulatory moieties to generate T-bodies with efficient antitumor reactivity.
引用
收藏
页码:123 / 126
页数:4
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