坏死性下垂
材料科学
癌细胞
癌症免疫疗法
免疫原性细胞死亡
免疫系统
裂谷1
免疫疗法
癌症
细胞生物学
程序性细胞死亡
细胞凋亡
癌症研究
化学
免疫学
生物
生物化学
遗传学
作者
Wooram Um,Hyewon Ko,Dong Gil You,Seungho Lim,Gijung Kwak,Man Kyu Shim,Suah Yang,Jeongjin Lee,Yeari Song,Kwangmeyung Kim,Jae Hyung Park
标识
DOI:10.1002/adma.201907953
摘要
Abstract Necroptosis, caspase‐independent programmed necrosis, has emerged as a therapeutic target to make dying cancer cells stimulants for antitumor immune responses. The clinical translations exploiting necroptosis, however, have been limited since most cancer cells downregulate receptor‐interacting protein kinase 3 (RIPK3) as a key enzyme for necroptosis. Herein, nanobubbles (NBs) that can trigger RIPK3‐independent necroptosis, facilitating cell‐membrane rupture via the acoustic cavitation effect are reported. The NBs, imbibing perfluoropentane as the gas precursor, are prepared using an amphiphilic polymer conjugate, composed of PEGylated carboxymethyl dextran as the hydrophilic backbone and chlorin e6 as the hydrophobic sonosensitizer. When exposed to ultrasound, the NBs efficiently promote the release of biologically active damage‐associated molecular patterns by inducing burst‐mediated cell‐membrane disintegration. Consequently, the necroptosis‐inducible NBs significantly improve antitumor immunity by maturation of dendritic cells and activation of CD8 + cytotoxic T cells both in vitro and in vivo. In addition, the combination of NBs and immune checkpoint blockade leads to complete regression of the primary tumor and beneficial therapeutic activity against metastatic tumors in an RIPK3‐deficient CT26 tumor‐bearing mouse model. Overall, the innovative NB that causes immunogenic cell death of cancer via RIPK3‐independent necroptosis is a promising enhancer for cancer immunotherapy.
科研通智能强力驱动
Strongly Powered by AbleSci AI