嵌合抗原受体
抗原
免疫系统
免疫疗法
趋化因子
癌症研究
T细胞
生物
益生菌
免疫学
细菌
遗传学
作者
Rosa L. Vincent,Candice R. Gurbatri,Fangda Li,Ana Vardoshvili,Courtney Coker,Jongwon Im,Edward R. Ballister,Mathieu Rouanne,Thomas Savage,Kenia de los Santos-Alexis,Andrew Redenti,Leonie Brockmann,Meghna Komaranchath,Nicholas Arpaia,Tal Danino
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2023-10-12
卷期号:382 (6667): 211-218
被引量:270
标识
DOI:10.1126/science.add7034
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.
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