Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz

Logo MUG-Forschungsportal

Gewählte Publikation:

SHR Neuro Krebs Kardio Lipid Stoffw Microb

Doerfler, P; Schoefmann, N; Cabral, G; Bauer, W; Berli, MC; Binder, B; Borst, C; Botter, S; French, LE; Goerge, T; Hafner, J; Hartmann, D; Høgh, A; Hoetzenecker, W; Holzer-Geissler, JCJ; Kamolz, LP; Kofler, K; Luger, T; Nischwitz, SP; Popovits, M; Rappersberger, K; Restivo, G; Schlager, JG; Schmuth, M; Stingl, G; Stockinger, T; Stroelin, A; Stuetz, A; Umlauft, J; Weninger, WP; Wolff-Winiski, B.
Development of a Cellular Assay as a Personalized Model for Testing Chronic Wound Therapeutics.
J Invest Dermatol. 2025; 145(3):631-644.e22 Doi: 10.1016/j.jid.2024.05.029
Web of Science PubMed FullText FullText_MUG

 

Co-Autor*innen der Med Uni Graz
Binder Barbara
Kamolz Lars-Peter
Nischwitz Sebastian
Altmetrics:

Dimensions Citations:

Plum Analytics:

Scite (citation analytics):

Abstract:
Exudates of nonhealing wounds contain drivers of pathogenicity. We utilized >800 exudates from nonhealing and healing wounds of diverse etiologies, collected by 3 different methods, to develop a wound-specific, cell-based functional biomarker assay. Human dermal fibroblast proliferation served as readout to (i) differentiate between healing and nonhealing wounds, (ii) follow the healing process of individual patients, and (iii) assess the effects of therapeutics for chronic wounds ex vivo. We observed a strong correlation between wound chronicity and inhibitory effects of individual exudates on fibroblast proliferation, with good diagnostic sensitivity (76-90%, depending on the sample collection method). Transition of a clinically nonhealing to a healing phenotype restored fibroblast proliferation and extracellular matrix formation while reducing inflammatory cytokine production. Transcriptional analysis of fibroblasts exposed to ex vivo nonhealing wound exudates revealed an induction of inflammatory cytokine and chemokine pathways and the unfolded protein response, indicating that these changes may contribute to the pathology of nonhealing wounds. Testing the wound therapeutics, PDGF and silver sulfadiazine, yielded responses in line with clinical experience and indicates the usefulness of the assay to search for and profile new therapeutics.
Find related publications in this database (using NLM MeSH Indexing)
Humans - administration & dosage
Wound Healing - administration & dosage
Fibroblasts - metabolism
Cell Proliferation - drug effects
Chronic Disease - administration & dosage
Precision Medicine - methods
Cells, Cultured - administration & dosage
Wounds and Injuries - therapy, pathology
Cytokines - metabolism
Biomarkers - metabolism
Skin - pathology, injuries, metabolism
Platelet-Derived Growth Factor - metabolism

Find related publications in this database (Keywords)
Biomarker
Functional assay
Transcriptomics
Wound exudate
Wound healing
© Med Uni Graz Impressum