Precision Tumor Recognition by T Cells With Combinatorial Antigen-Sensing Circuits

被引:753
作者
Roybal, Kole T. [1 ,2 ,3 ]
Rupp, Levi J. [1 ,2 ,3 ]
Morsut, Leonardo [1 ,2 ,3 ]
Walker, Whitney J. [1 ,2 ,3 ]
McNally, Krista A. [1 ,2 ,3 ]
Park, Jason S. [1 ,2 ,3 ]
Lim, Wendell A. [1 ,2 ,3 ]
机构
[1] Univ Calif San Francisco, Dept Cellular & Mol Pharmacol, San Francisco, CA 94158 USA
[2] Univ Calif San Francisco, Ctr Syst & Synthet Biol, San Francisco, CA 94158 USA
[3] Howard Hughes Med Inst, San Francisco, CA 94158 USA
关键词
CANCER; THERAPIES; TOOLS; ERBB2;
D O I
10.1016/j.cell.2016.01.011
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
T cells can be re-directed to kill cancer cells using chimeric antigen receptors (CARs) or T cell receptors (TCRs). This approach, however, is constrained by the rarity of tumor-specific single antigens. Targeting antigens also found on bystander tissues can cause life-threatening adverse effects. A powerful way to enhance ON-target activity of therapeutic T cells is to engineer them to require combinatorial antigens. Here, we engineer a combinatorially activated T cell circuit in which a synthetic Notch receptor for one antigen induces the expression of a CAR for a second antigen. These dual-receptor AND-gate T cells are only armed and activated in the presence of dual antigen tumor cells. These T cells show precise therapeutic discrimination in vivo-sparing single antigen "bystander'' tumors while efficiently clearing combinatorial antigen "disease'' tumors. This type of precision dual-receptor circuit opens the door to immune recognition of a wider range of tumors.
引用
收藏
页码:770 / 779
页数:10
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