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 M. Savage,Kenia de los Santos,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:284
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI