A Mitochondria-Targeted NIR-II AIEgen Induced Pyroptosis for Enhanced Tumor Immunotherapy

被引:11
|
作者
Yu, Kaiwu [1 ]
Ye, Binglin [2 ]
Yang, Huang [3 ]
Xu, Xinxin [1 ]
Mao, Zhengwei [2 ,3 ]
Zhang, Qinghua [1 ]
Tian, Mei [4 ,5 ]
Zhang, Haoke [3 ]
Zhang, Hong [4 ,5 ]
He, Qinggang [1 ]
机构
[1] Zhejiang Univ, Coll Chem & Biol Engn, Hangzhou 310058, Peoples R China
[2] Zhejiang Univ, Sch Med, Affiliated Hosp 2, Dept Hepatobiliary & Pancreat Surg, Hangzhou 310009, Peoples R China
[3] Zhejiang Univ, Dept Polymer Sci & Engn, MOE Key Lab Macromol Synth & Functionalizat, Hangzhou 310027, Peoples R China
[4] Zhejiang Univ, Sch Med, Hosp 2, Dept Nucl Med, Hangzhou 310009, Peoples R China
[5] Zhejiang Univ, Hosp 2, Sch Med, PET Ctr, Hangzhou 310009, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
aggregation-induced emission; immune checkpoint therapy; immunogenic cell death; NIR-II imaging; pyroptosis; CELL-DEATH; CANCER; FLUOROPHORES; ACTIVATION; CASPASES; ROLES;
D O I
10.1002/adhm.202301693
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Cancer immunotherapy is a favorable strategy for facilitating anti-tumor immunity, but it shows limited benefits in clinical practice owing to the immunosuppressive tumor microenvironment. Pyroptosis shows great immunostimulatory effect on tumor, whereas the lack of pyroptotic inducer with imaging property has restricted its progress in tumor theranostics. Herein, a mitochondria-targeted aggregation-induced emission (AIE) luminogen (TPA-2TIN) with NIR-II emission is designed for highly efficient induction of tumor cell pyroptosis. The fabricated TPA-2TIN nanoparticles can be efficiently taken up by tumor cells and selectively accumulated in tumor for a long term observed by NIR-II fluorescence imaging. More importantly, the TPA-2TIN nanoparticles can effectively stimulate immune responses both in vitro and in vivo mediated by the mitochondrial dysfunctions and the subsequent activation of the pyroptotic pathway. Ultimately, the reversal of the immunosuppressive tumor microenvironment significantly enhances the immune checkpoint therapy. This study paves a new avenue for adjuvant immunotherapy of cancer.
引用
收藏
页数:9
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