Light-Triggered Bismuth-Based Nanosphere as a Dual-Inductive Nanomedicine for Antitumor Immunotherapy

被引:0
|
作者
Yang, Zhijin [1 ,2 ]
Du, Jun [3 ]
Chen, Mengya [1 ,2 ]
Liu, Pingsheng [1 ]
Wang, Qian [3 ]
Wu, Sijia [3 ]
Xue, Zhiwei [1 ]
Zhang, Yule [1 ]
Zhuang, Songlin [1 ,2 ]
Zhang, Dawei [1 ,2 ,4 ]
Zheng, Lulu [1 ,2 ]
Li, Yuhao [3 ]
机构
[1] Univ Shanghai Sci & Technol, Engn Res Ctr Opt Instrument & Syst, Shanghai Key Lab Modern Opt Syst, Minist Educ, Shanghai 200093, Peoples R China
[2] Univ Shanghai Sci & Technol, Shanghai Engn Res Ctr Environm Biosafety Instrumen, Shanghai 200093, Peoples R China
[3] Univ Shanghai Sci & Technol, Inst Bismuth, Shanghai Collaborat Innovat Ctr Energy Therapy Tum, Sch Mat & Chem, Shanghai 200093, Peoples R China
[4] Tongji Univ, Shanghai Inst Intelligent Sci & Technol, Shanghai 200092, Peoples R China
基金
中国国家自然科学基金;
关键词
phototherapy; dual-inductive nanomedicine; apoptosis; necroptosis; immunotherapy; NECROPTOSIS; CELLS; DRUGS;
D O I
10.1021/acsanm.4c05711
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The immunosuppressive microenvironment of the tumor is an important factor that seriously affects the effect of tumor immunotherapy. Programmed cell death, including apoptosis and necroptosis, has shed light on antitumor therapy and could synergistically activate the antitumor immunity. Herein, S-doped bismuth oxide lychee-like nanospheres (BiOSSs) are presented to realize apoptosis- and necroptosis-mediated tumor treatment strategies. Under laser irradiation, BiOSS demonstrated exceptional capabilities in reactive oxygen species generation and heat production. After BiOSS-triggered antitumor phototherapy, the characteristic markers of apoptosis and necroptosis were significantly changed and the cell membrane was damaged. Moreover, BiOSS-induced apoptosis/necroptosis could result in an immune response and obtain exciting treatment effects. The flow cytometry results revealed that costimulatory molecules CD86 and CD80 expressions in dendritic cells (DCs) were increased after BiOSS-triggered apoptosis/necroptosis, indicating DC maturation, further promoting the activation of CD8+ cytotoxic T lymphocytes, finally inhibiting tumor lung metastasis. Overall, BiOSS-triggered phototherapy shows a strategy for antitumor immunotherapy with exciting potential for clinical application.
引用
收藏
页码:1021 / 1032
页数:12
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