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.

Keywords:
Chimeric antigen receptor Antigen Immune system Immunotherapy Chemokine Cancer research T cell Biology Probiotic Immunology Bacteria

Metrics

194
Cited By
46.09
FWCI (Field Weighted Citation Impact)
65
Refs
1.00
Citation Normalized Percentile
Is in top 1%
Is in top 10%

Citation History

Topics

CAR-T cell therapy research
Health Sciences →  Medicine →  Oncology
Cancer Research and Treatments
Life Sciences →  Biochemistry, Genetics and Molecular Biology →  Biotechnology
Virus-based gene therapy research
Life Sciences →  Biochemistry, Genetics and Molecular Biology →  Genetics
© 2026 ScienceGate Book Chapters — All rights reserved.