A Bimetallic Nanomodulator to Reverse Immunosuppression via Sonodynamic-Ferroptosis and Lactate Metabolism Modulation

被引:13
作者
Deng, Xi [1 ,2 ]
Zhu, Yutong [1 ,2 ]
Dai, Zideng [1 ,2 ,3 ]
Liu, Qing [1 ,2 ]
Song, Ze [1 ,2 ]
Liu, Tianzhi [1 ,2 ]
Huang, Yuefeng [1 ,2 ,3 ]
Chen, Hangrong [1 ,2 ,3 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Ceram, State Key Lab High Performance Ceram & Superfine M, Shanghai 200050, Peoples R China
[2] Univ Chinese Acad Sci, Ctr Mat Sci & Optoelect Engn, Beijing 100049, Peoples R China
[3] Univ Chinese Acad Sci, Hangzhou Inst Adv Study, Sch Chem & Mat Sci, Hangzhou 310024, Peoples R China
基金
中国国家自然科学基金;
关键词
ferroptosis; immune checkpoint blockade; immunotherapy; lactate; sonodynamic therapy; CANCER-IMMUNOTHERAPY; LACTIC-ACID; TUMOR; STRATEGIES;
D O I
10.1002/smll.202404580
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Triple-negative breast cancer (TNBC) responds poorly to immunotherapy due to insufficient immunogenicity and highly immunosuppressive tumor microenvironment (TME). Herein, an intelligent calcium/cobalt-based nanomodulator (Ca,Co)CO3-LND-TCPP@F127-TA (abbreviated as CCLT@FT) is developed to act as a sonodynamic-ferroptosis inducer and metabolic immunoadjuvant to enhance anti-tumor immunotherapy. More details, simultaneous reactive oxygen species (ROS) generation and glutathione (GSH) depletion can be achieved due to the existence of Co2+/Co3+ redox couple in CCLT@FT. Meanwhile, mitochondrial Ca2+ overload and tetrakis(4-carboxyphenyl) porphyrin (TCPP)-mediated sonodynamic therapy (SDT) further amplify the oxidative stress and promote ferroptosis in tumor cells. More impressively, CCLT@FT can modulate lactate metabolism by doping with cobalt and loading with lonidamine (LND, an inhibitor of MCT4), thereby reversing the high-lactate immunosuppressive TME. Furthermore, the combination with immune checkpoint blockade (ICB) therapy is found to achieve superior anti-tumor immunity, which in turn promotes ferroptosis of tumor cells by downregulating SLC7A11 protein, ultimately creating a "cycle" therapy. Overall, this work demonstrates a novel strategy for enhancing anti-tumor immunotherapy based on a closed-loop enhancement therapeutic route between CCLT@FT inducing ferroptosis/lactate metabolism modulation and ICB therapy, providing an alternative and important reference for effective immunotherapy of TNBC. A novel bimetallic nanomodulator (CCLT@FT) is constructed, which can serve as a SDT-enhanced ferroptosis inducer and metabolic immunoadjuvant for TNBC concurrently to achieve regulation of the immunosuppressive TME and highly efficient anti-tumor immunotherapy. More importantly, a closed-loop enhancement therapeutic route between CCLT@FT inducing ferroptosis/lactate metabolism modulation and PD-L1 immune checkpoint is achieved, exhibiting great promise. image
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页数:15
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