材料科学
氢氧化物
肿瘤微环境
透明质酸
锰
内吞作用
免疫疗法
癌症研究
肿瘤细胞
生物
生物化学
免疫系统
化学
免疫学
冶金
无机化学
细胞
遗传学
作者
Chengyao Huang,Ke Zhang,Ren Yu,Xihong Liu,Yan Li,B Yang,Peiran Chen,Mingyue Zhang,Xiaotong Lu,Yuhong Zhuo,Chao Qi,Kaiyong Cai
标识
DOI:10.1016/j.actbio.2024.08.045
摘要
Tumor immunotherapy has gained more and more attention in tumor treatment. However, the accumulation of lactic acid in tumor tissue inhibits the response of immune cells to form an immunosuppressive microenvironment (ISME). To reverse the ISME, an acid-responsive nanoplatform (termed as MLLN@HA) is reported for synergistically enhanced tumor immunotherapy. MLLN@HA is constructed by the co-loading of lactate oxidase (LOX) and DNA repair inhibitor (NU7441) in a manganese-doped layered double hydroxide (Mn-LDH), and then modified with hyaluronic acid (HA) for tumor-targeted delivery. After endocytosis by tumor cells, MLLN@HA decomposes and releases LOX, NU7441 and Mn
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