A Copper-Manganese Based Nanocomposite Induces Cuproptosis and Potentiates Anti-Tumor Immune Responses

被引:0
作者
Xie, Luoyingzi [1 ,2 ,3 ]
Gong, Jie [1 ,2 ,4 ,5 ]
He, Zhiqiang [6 ]
Zhang, Weinan [7 ]
Wang, Haoyu [1 ,2 ]
Wu, Shitao [1 ,2 ,8 ]
Wang, Xianxing [1 ,2 ]
Sun, Pijiang [1 ,2 ]
Cai, Lei [1 ,2 ]
Wu, Zhongjun [3 ]
Wang, Huaizhi [1 ,2 ]
机构
[1] Chongqing Univ, Chongqing Gen Hosp, Inst Hepatopancreatobiliary Surg, Chongqing 401147, Peoples R China
[2] Chongqing Key Lab Intelligent Med Engn Hepatopancr, Chongqing 401147, Peoples R China
[3] Chongqing Med Univ, Affiliated Hosp 1, Dept Hepatobiliary Surg, Chongqing 400010, Peoples R China
[4] Chongqing Med Univ, Sch Clin Med, Chongqing 400016, Peoples R China
[5] Leshan Peoples Hosp, Dept Hepatobiliary Surg, Leshan 614000, Peoples R China
[6] 958th Hosp Chinese Peoples Liberat Army, Southwest Hosp, Dept Dermatol, Jiangbei Area, Chongqing 400020, Peoples R China
[7] Chongqing Med Univ, Affiliated Hosp 2, Dept Urinary Nephropathy Ctr, Chongqing 400000, Peoples R China
[8] Chongqing Med Univ, Grad Sch, Chongqing 400016, Peoples R China
基金
中国国家自然科学基金;
关键词
CD8(+) T cells; cuproptosis; dendritic cells; manganese; tumor-associated macrophages; CD8(+) T-CELLS; CANCER; EPIDEMIOLOGY; EXHAUSTION;
D O I
10.1002/smll.202412174
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Cancer is one of the most important challenges worldwide with an increasing incidence. However, most of patients with malignant cancer receiving traditional therapies have tumor recurrence and short-term 5-year survival. Herein, a novel Cu2O-MnO@PEG (CMP) nanomaterial is developed to treat tumors. CMP directly mediates cuproptosis in tumor cells. Meanwhile, CMP potentiates anti-tumor immune responses in the tumor microenvironment (TME) to induce tumor regression. CMP improves the tumor antigen processing and presentation of dendritic cells and tumor-associated macrophages, and further promotes CD8(+) T cell responses, especially for cytotoxic CD8(+) T cells and transitory exhausted CD8(+) T cells. Additionally, CMP downregulates the proportion of Treg cells and CTLA-4 expression on Treg cells. Notably, CMP induces systemic immune responses against distant tumors and long-term immune memory. Furthermore, CMP synergized with PD-L1 mAb promotes tumor inhibition and sustains the anti-tumor efficacy post PD-L1 mAb treatment. Collectively, this strategy has the clinically therapeutic potential for tumors by facilitating cuproptosis in tumor cells and anti-tumor immune responses.
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页数:16
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