Probiotic-guided CAR-T cells for solid tumor targeting

Rosa L. Vincent(Columbia University), Candice R. Gurbatri(Columbia University), Fangda Li(Columbia University), Ana Vardoshvili(Columbia University), Courtney Coker(Columbia University), Jongwon Im(Columbia University), Edward R. Ballister(Columbia University), Mathieu Rouanne(Columbia University Irving Medical Center), Thomas Savage(Columbia University), Kenia de los Santos-Alexis(Columbia University), Andrew Redenti(Columbia University), Leonie Brockmann(Columbia University), Meghna Komaranchath(Columbia University), Nicholas Arpaia(Columbia University Irving Medical Center), Tal Danino(Columbia University Irving Medical Center)
Science
October 12, 2023
Cited by 233Open Access
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Abstract

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.


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