Department of Biomedical Engineering, Columbia University, New York, NY 10027, USA.
Department of Microbiology and Immunology, Vagelos College of Physicians and Surgeons of Columbia University, New York, NY 10032, USA.
Science. 2023 Oct 13;382(6667):211-218. doi: 10.1126/science.add7034. Epub 2023 Oct 12.
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.
肿瘤抗原靶向治疗(如嵌合抗原受体(CAR)-T 细胞)面临的一个主要挑战是鉴定合适的靶点,这些靶点在异质性实体瘤上特异性和均匀表达。相比之下,某些种类的细菌选择性地定植于免疫特权的肿瘤核心,并且可以被工程化为用于治疗性递送的抗原非依赖性平台。为了弥合这些方法之间的差距,我们开发了一种益生菌引导的 CAR-T 细胞(ProCAR)平台,其中肿瘤定植的益生菌释放合成靶标,对肿瘤组织进行标记,以便 CAR 介导的原位裂解。该系统在多种人源和鼠源癌症的异种移植和同基因模型中证明了 CAR-T 细胞的激活和抗原非依赖性细胞裂解,既安全又有效。我们进一步设计了多功能益生菌,共同释放趋化因子以增强 CAR-T 细胞的募集和治疗反应。