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Soluble CD83 improves and accelerates wound healing by the induction of pro-resolving macrophages.

Authors :
Royzman D
Peckert-Maier K
Stich L
König C
Wild AB
Tauchi M
Ostalecki C
Kiesewetter F
Seyferth S
Lee G
Eming SA
Fuchs M
Kunz M
Stürmer EK
Peters EMJ
Berking C
Zinser E
Steinkasserer A
Source :
Frontiers in immunology [Front Immunol] 2022 Sep 30; Vol. 13, pp. 1012647. Date of Electronic Publication: 2022 Sep 30 (Print Publication: 2022).
Publication Year :
2022

Abstract

To facilitate the recovery process of chronic and hard-to-heal wounds novel pro-resolving treatment options are urgently needed. We investigated the pro-regenerative properties of soluble CD83 (sCD83) on cutaneous wound healing, where sCD83 accelerated wound healing not only after systemic but also after topical application, which is of high therapeutic interest. Cytokine profile analyses revealed an initial upregulation of inflammatory mediators such as TNFα and IL-1β, followed by a switch towards pro-resolving factors, including YM-1 and IL-10, both expressed by tissue repair macrophages. These cells are known to mediate resolution of inflammation and stimulate wound healing processes by secretion of growth factors such as epidermal growth factor (EGF) and vascular endothelial growth factor (VEGF), which promote vascularization as well as fibroblast and keratinocyte differentiation. In conclusion, we have found strong wound healing capacities of sCD83 beyond the previously described role in transplantation and autoimmunity. This makes sCD83 a promising candidate for the treatment of chronic- and hard-to-heal wounds.<br />Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.<br /> (Copyright © 2022 Royzman, Peckert-Maier, Stich, König, Wild, Tauchi, Ostalecki, Kiesewetter, Seyferth, Lee, Eming, Fuchs, Kunz, Stürmer, Peters, Berking, Zinser and Steinkasserer.)

Details

Language :
English
ISSN :
1664-3224
Volume :
13
Database :
MEDLINE
Journal :
Frontiers in immunology
Publication Type :
Academic Journal
Accession number :
36248909
Full Text :
https://doi.org/10.3389/fimmu.2022.1012647