Probiotic-guided CAR-T cells for solid tumor targeting

Author:

Vincent Rosa L.1ORCID,Gurbatri Candice R.1ORCID,Li Fangda2,Vardoshvili Ana1,Coker Courtney1ORCID,Im Jongwon1ORCID,Ballister Edward R.12ORCID,Rouanne Mathieu23ORCID,Savage Thomas2ORCID,de los Santos-Alexis Kenia2ORCID,Redenti Andrew12,Brockmann Leonie2,Komaranchath Meghna1,Arpaia Nicholas23ORCID,Danino Tal134ORCID

Affiliation:

1. Department of Biomedical Engineering, Columbia University, New York, NY 10027, USA.

2. Department of Microbiology and Immunology, Vagelos College of Physicians and Surgeons of Columbia University, New York, NY 10032, USA.

3. Herbert Irving Comprehensive Cancer Center, Columbia University, New York, NY 10032, USA.

4. Data Science Institute, Columbia University, New York, NY 10027, USA.

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.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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