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Spatial Isolation of Single Copper(I) Sites for Cascade Enzyme-Like Catalysis and Simultaneous Ferroptosis/Cuproptosis Boosted Immunotherapy
被引:0
|作者:
Zhang, Yuanyuan
[1
]
Ya, Shengnan
[2
]
Huang, Jingnan
[3
]
Ju, Yangyang
[1
]
Fang, Xueyang
[1
]
Ouyang, Xinteng
[1
]
Zeng, Qingdong
[1
]
Zhou, Xinyao
[4
]
Yan, Xiyun
[5
,6
]
Nie, Guohui
[1
]
Fan, Kelong
[5
,6
]
Zhang, Bin
[1
]
机构:
[1] Shenzhen Univ, Shenzhen Key Lab Nanozymes & Translat Canc Res, Shenzhen Peoples Hosp 2, Affiliated Hosp 1,Dept Otolaryngol,Shenzhen Inst T, Shenzhen, Peoples R China
[2] Wannan Med Coll, Sch Med Imageol, Wuhu, Peoples R China
[3] Southern Univ Sci & Technol, Affiliated Hosp 1, Shenzhen Peoples Hosp, Dept Gastroenterol, Shenzhen, Peoples R China
[4] Univ Maryland, Fischell Dept Bioengn, College Pk, MD USA
[5] Chinese Acad Sci, CAS Ctr Excellence Biomacromolecules, CAS Engn Lab Nanozyme, Key Lab Biomacromolecules CAS,Inst Biophys, Beijing, Peoples R China
[6] Henan Acad Innovat Med Sci, Nanozyme Lab Zhongyuan, Zhengzhou, Henan, Peoples R China
来源:
基金:
中国国家自然科学基金;
关键词:
cuproptosis;
ferroptosis;
immunogenic cell death;
photothermal-amplified ROS storms;
single-site nanozyme;
D O I:
10.1002/EXP.20240275
中图分类号:
TB3 [工程材料学];
学科分类号:
0805 ;
080502 ;
摘要:
Nanozyme-based immunogenic cell death (ICD) inducers that effectively induce a strong immune response via enzyme-like process have attracted great attention, but how to ensure controllable active sites and maximize site utilization remains a problem. Here, we report a structurally well-defined and highly functional single-site copper(I) nanomodulators termed CuNTD, constructed by precisely anchoring atomically dispersed self-assembly S-Cu(I)-S sites onto a two-dimensional Ti3C2 surface. Leveraging Cu+ with a higher catalytic efficiency than Cu2+, CuNTD generates reactive oxygen species (ROS) storms through photothermal-enhanced cascade catalysis, further inducing mitochondrial dysfunction, ferroptosis and cuproptosis. Multifunctional CuNTD triggers strong ICD through cascade-regulatory pathways of photothermal-amplified ROS storms, cuproptosis and ferroptosis, effectively promoting dendritic cell maturation while reducing monotherapies side effects and resistance. In vivo, CuNTD combined with FDA-approved immunoadjuvants significantly prolong the survival of mice. With its demonstrated biosafety and high efficiency as an ICD inducer, this study provides a promising framework for advancing augmented tumor immunotherapy with significant clinical potential.
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