rFSAV promotes Staphylococcus aureus-infected bone defect healing via IL-13- mediated M2 macrophage polarization

Copyright © 2023. Published by Elsevier Inc.

Bibliographische Detailangaben
Veröffentlicht in:Clinical immunology (Orlando, Fla.). - 1999. - 255(2023) vom: 15. Okt., Seite 109747
1. Verfasser: Zhang, Yanhao (VerfasserIn)
Weitere Verfasser: Yang, Feng, Sun, Dong, Xu, Limin, Shi, Yaojia, Qin, Leilei, Zhao, Liqun, Wang, Liting, Sun, Wei, Wu, Hongri, Lu, Dongshui, Zhang, Weijun, Luo, Ping, Cheng, Ping, Zou, Quanming, Zeng, Hao
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2023
Zugriff auf das übergeordnete Werk:Clinical immunology (Orlando, Fla.)
Schlagworte:Journal Article Bone infection Interleukin-13 Macrophage polarization Staphylococcus aureus Vaccine
Beschreibung
Zusammenfassung:Copyright © 2023. Published by Elsevier Inc.
Staphylococcus aureus (S. aureus) contamination commonly occurs in orthopedic internal fixation operations, leading to a delayed healing of the defected bone tissue. However, antibiotic treatments are ineffective in dealing with S. aureus bone infections due to the rise in multiple antimicrobial resistances. Here, we reported the protective effects of a recombinant five-antigen S. aureus vaccine (rFSAV) in an S. aureus infected bone defect model. In this study, we found the number of M2 macrophages markedly increased in the defect site and played a critical role in the healing of defected bone mediated by rFSAV. Mechanistically, rFSAV mediated increased level of IL-13 in bone defect site predominant M2 macrophage polarization. In summary, our study reveals a key role of M2 macrophage polarization in the bone regeneration process in S. aureus infection induced bone defect, which provide a promising application of rFSAV for the treatment of bone infection for orthopedic applications
Beschreibung:Date Revised 28.09.2023
published: Print-Electronic
Citation Status Publisher
ISSN:1521-7035
DOI:10.1016/j.clim.2023.109747