光动力疗法
免疫系统
癌症研究
转移
免疫疗法
癌细胞
肿瘤微环境
癌症免疫疗法
材料科学
医学
化学
癌症
免疫学
内科学
有机化学
作者
Rong Chen,Tingting Hu,Lu Yu,Shuqing Yang,Min Zhang,Chaoliang Tan,Ruizheng Liang,Yuji Wang
出处
期刊:Small
[Wiley]
日期:2024-10-02
被引量:4
标识
DOI:10.1002/smll.202404211
摘要
Abstract Photodynamic therapy (PDT) is demonstrated to be effective in inducing antitumor immune responses for tumor metastasis treatment. However, tumor hypoxia, inferior tissue penetration of light, and low singlet oxygen ( 1 O 2 ) quantum yield significantly hamper the efficacy of PDT, thus weakening its immune function. Moreover, PDT‐mediated neutrophil extracellular traps (NETs) formation can further reduce the therapeutic effectiveness. Herein, the use of defect‐rich CoMo‐layered double hydroxide (DR‐CoMo‐LDH) nanosheets as a carrier to load a typical peptidyl arginine deiminase 4 inhibitor, i.e., YW4‐03, to construct a multifunctional nanoagent (403@DR‐LDH) for PDT/immunotherapy, is reported. Specifically, 403@DR‐LDH inherits excellent 1 O 2 generation activity under 1550 nm laser irradiation and improves the half‐life of YW4‐03. Meanwhile, 403@DR‐LDH plus 1550 nm laser irradiation can stimulate immunogenic cell death to promote the maturation of dendric cells and activation/infiltration of T cells and significantly downregulate H3cit protein expression to inhibit NETs formation, synergistically promoting the antitumor metastasis effect. Taken together, 403@DR‐LDH can kill cancer cells and inhibit tumor growth/metastasis under 1550 nm laser irradiation. Single‐cell analysis indicates that 403@DR‐LDH can regulate the ratio of immune cells and immune‐related proteins to improve the tumor immune microenvironment, showing strong efficacy to inhibit the tumor growth, metastasis, and recurrence.
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