Manganese-Based Biofunctional 2D Nanosheets Enabled In Situ Macrophage Engineering for Precise Eradication of Osteomyelitis
Language English Country Germany Media print-electronic
Document type Journal Article
Grant support
20240484527
Beijing Nova Program of Science and Technology
52302343
National Natural Science Foundation of China
RCPT-20220029
Beijing Institute of Technology Teli Young Fellow Program
LL2101
ERC-CZ program
CZ.02.1.01/0.0/0.0/15_003/0000444
Advanced Functional Nanorobots
9220061
City University of Hong Kong Donation Research Grants
DON-RMG 9229021
City University of Hong Kong Donation Research Grants
- Keywords
- biofunctional nanosheets, macrophage engineering, metalloimmunotherapy, osteomyelitis, phagolysosomal killing,
- MeSH
- Anti-Bacterial Agents pharmacology chemistry MeSH
- Phagocytosis drug effects MeSH
- Humans MeSH
- Macrophages * metabolism drug effects MeSH
- Manganese * chemistry pharmacology MeSH
- Disease Models, Animal MeSH
- Mice, Inbred C57BL MeSH
- Mice MeSH
- Nanostructures * chemistry MeSH
- Neutrophils metabolism MeSH
- Osteomyelitis * drug therapy microbiology pathology therapy MeSH
- RAW 264.7 Cells MeSH
- Staphylococcal Infections * drug therapy MeSH
- Staphylococcus aureus drug effects MeSH
- Animals MeSH
- Check Tag
- Humans MeSH
- Mice MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Anti-Bacterial Agents MeSH
- Manganese * MeSH
Efficient treatment of osteomyelitis caused by Staphylococcus aureus is a great clinical challenge due to bacterial resistance and immune evasion issues. Macrophages play a crucial role in the fight against S. aureus but suffer from deficiencies in function in the infectious milieu leading to persistent infection. Here, a strategy of exploiting aged neutrophil membrane (aNM) is developed to camouflage 2D MnPSe3 nanosheets (MPS NSs), denoted as aNM@MPS, to mediate in situ macrophage engineering, thereby potentiating macrophages to eradicate refractory osteomyelitis. When administered systematically, the biofunctional aNM@MPS ensures selectivity for osteomyelitis lesions, enhanced bone marrow retention, and subsequent phagocytosis by macrophages. In the mouse model of osteomyelitis, the aNM@MPS enables dysfunctional macrophages to digest intracellular bacteria by generating highly toxic hydroxyl radicals and sequentially reprogramming bactericidal immunity through manganese ion-mediated immune activation, which synergistically terminates persistent infection-initiated pathological cascades and subsequently reestablish host-directed bactericidal potency, thereby conferring a satisfactory osteoprotective effect. These findings demonstrate that macrophages in the skeletal infectious milieu can be precisely remodeled via the lesion-macrophage dual-targeting metalloimmunotherapy strategy, which holds potential for osteomyelitis treatment.
Department of Neurology Beijing Tiantan Hospital Capital Medical University Beijing 100070 China
School of Interdisciplinary Science Beijing Institute of Technology Beijing 100081 China
School of Medical Technology Beijing Institute of Technology Beijing 100081 China
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