Probiotic-guided CAR-T cells for solid tumor targeting

被引:42
|
作者
Vincent, Rosa L. [1 ]
Gurbatri, Candice R. [1 ]
Li, Fangda [2 ]
Vardoshvili, Ana [1 ]
Coker, Courtney [1 ]
Im, Jongwon [1 ]
Ballister, Edward R. [1 ,2 ]
Rouanne, Mathieu [2 ,3 ]
Savage, Thomas [2 ]
de los Santos-Alexis, Kenia [2 ]
Redenti, Andrew [2 ]
Brockmann, Leonie [2 ]
Komaranchath, Meghna [1 ]
Arpaia, Nicholas [2 ,3 ]
Danino, Tal [1 ,3 ,4 ]
机构
[1] Columbia Univ, Dept Biomed Engn, New York, NY 10027 USA
[2] Columbia Univ, Dept Microbiol & Immunol, Vagelos Coll Phys & Surg, New York, NY 10032 USA
[3] Columbia Univ, Herbert Irving Comprehens Canc Ctr, New York, NY 10032 USA
[4] Columbia Univ, Data Sci Inst, New York, NY 10027 USA
关键词
CHIMERIC ANTIGEN RECEPTORS; PHASE-I; AFFINITY; TLR5;
D O I
10.1126/science.add7034
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
A major challenge facing tumor-antigen targeting therapies such as chimeric antigen receptor (CAR)-T cells is the identification of suitable targets that are specifically and uniformly expressed on heterogeneous solid tumors. By contrast, certain species of bacteria selectively colonize immune-privileged tumor cores and can be engineered as antigen-independent platforms for therapeutic delivery. To bridge these approaches, we developed a platform of probiotic-guided CAR-T cells (ProCARs), in which tumor-colonizing probiotics release synthetic targets that label tumor tissue for CAR-mediated lysis in situ. This system demonstrated CAR-T cell activation and antigen-agnostic cell lysis that was safe and effective in multiple xenograft and syngeneic models of human and mouse cancers. We further engineered multifunctional probiotics that co-release chemokines to enhance CAR-T cell recruitment and therapeutic response.
引用
收藏
页码:211 / 218
页数:8
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