材料科学
细胞毒性T细胞
免疫系统
肿瘤微环境
细胞内
细菌
体内
颗粒酶
免疫疗法
透明质酸
噬菌体疗法
癌症研究
生物
免疫学
体外
CD8型
细胞生物学
噬菌体
生物化学
生物技术
大肠杆菌
穿孔素
基因
遗传学
作者
Shiyu Zhang,Han Zhu,Xiaohui Peng,Yang Zhou,Riming Huang,Yifan Wang,Shu‐Lin Liu,Zhigang Wang
标识
DOI:10.1002/adma.202503087
摘要
Abstract Tumor‐colonizing bacteria can impede the efficacy of cancer treatments and elevate the risk of metastatic spread. While cytotoxic T lymphocytes (CTLs) are essential for destroying tumor cells, they lack the ability to eliminate bacteria. Here, the artificial T cells (ATC) are presented for tumors, particularly those colonized with intracellular bacteria. The ATC is composed of a hydrogel framework made of disulfide‐linked chitosan and hyaluronic acid, encapsulating T cell‐derived granzyme B and phage‐derived holin. This design leverages the tumor microenvironment for the targeted release of these antitumor and antibacterial agents to precisely kill tumor cells and intracellular bacteria. In vivo studies demonstrate the debris from ATC‐mediated destruction acts as an immune stimulator, promoting immune cell infiltration and inhibiting tumor migration. This work highlights the potential of ATC therapy in achieving targeted treatment and robust anti‐tumor immunity, advancing the field of artificial cell technologies for precision medicine.
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