材料科学
细胞毒性T细胞
免疫系统
肿瘤微环境
癌症治疗
细胞内
颗粒酶B
体内
颗粒酶
免疫疗法
透明质酸
T细胞
细胞毒性
渗透(HVAC)
细胞疗法
细胞
癌细胞
癌症免疫疗法
肿瘤细胞
癌症研究
癌症
医学
癌症治疗
靶向治疗
免疫学
体外
CD8型
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI