Abstract
Introduction: Natural products have been shown to an important source of therapeutics for human disease. In this study, we aimed to identify natural compounds as potential therapeutics for epidermolysis bullosa acquisita (EBA), an autoimmune disease caused by autoantibodies to type VII collagen (COL7). Methods: Utilizing an in vitro experimental system, we screened a natural product library composed of 800 pure compounds for their inhibitory effect on COL7-anti-COL7 IgG immune complex (IC)-mediated neutrophil activation and on neutrophil-mediated tissue damage. Results: Three natural compounds, namely luteolin peracetate, gossypol, and gossypolone were capable in inhibiting the IC-induced neutrophil adhesion and oxygen burst in vitro. Furthermore, luteolin peracetate and gossypolone were able to inhibit the anti-COL7 IgG induced dermal-epidermal separation in an ex vivo model for EBA. Discussion: In summary, this study demonstrates that luteolin peracetate and gossypolone are potential therapeutics for experimental EBA, which deserves further investigation.
| Originalsprache | Englisch |
|---|---|
| Aufsatznummer | 1196116 |
| Zeitschrift | Frontiers in Immunology |
| Jahrgang | 14 |
| Seiten (von - bis) | 1196116 |
| ISSN | 1664-3224 |
| DOIs | |
| Publikationsstatus | Veröffentlicht - 2023 |
Fördermittel
This work was supported by funding from the German Research Foundation (DFG: RTG 1727, RTG 2633, YU 142/1-3 (No. 272606465), Excellence Cluster “Precision Medicine in Inflammation”, TI4), the German Ministry of Education and Research (BMBF) via German Center for Lung Research (DZL). Acknowledgments
UN SDGs
Dieser Output leistet einen Beitrag zu folgendem(n) Ziel(en) für nachhaltige Entwicklung
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SDG 3 – Gesundheit und Wohlergehen
Strategische Forschungsbereiche und Zentren
- Forschungsschwerpunkt: Infektion und Entzündung - Zentrum für Infektions- und Entzündungsforschung Lübeck (ZIEL)
- Zentren: Center for Research on Inflammation of the Skin (CRIS)
DFG-Fachsystematik
- 2.21-05 Immunologie
- 2.22-19 Dermatologie
- 2.22-22 Klinische Immunologie und Allergologie
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