Topical Diacerein Decreases Skin and Splenic CD11c + Dendritic Cells in Psoriasis

Psoriasis is an inflammatory skin disease characterized by increased neo-vascularization, keratinocyte hyperproliferation, a pro-inflammatory cytokine milieu and immune cell infiltration. Diacerein is an anti-inflammatory drug, modulating immune cell functions, including expression and production of...

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Published inInternational journal of molecular sciences Vol. 24; no. 5; p. 4324
Main Authors Brunner, Susanne M, Ramspacher, Andrea, Rieser, Caroline, Leitner, Julia, Heil, Hannah, Ablinger, Michael, Tevini, Julia, Wimmer, Monika, Koller, Andreas, Piñón Hofbauer, Josefina, Felder, Thomas K, Bauer, Johann W, Kofler, Barbara, Lang, Roland, Wally, Verena
Format Journal Article
LanguageEnglish
Published Switzerland MDPI AG 21.02.2023
MDPI
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Summary:Psoriasis is an inflammatory skin disease characterized by increased neo-vascularization, keratinocyte hyperproliferation, a pro-inflammatory cytokine milieu and immune cell infiltration. Diacerein is an anti-inflammatory drug, modulating immune cell functions, including expression and production of cytokines, in different inflammatory conditions. Therefore, we hypothesized that topical diacerein has beneficial effects on the course of psoriasis. The current study aimed to evaluate the effect of topical diacerein on imiquimod (IMQ)-induced psoriasis in C57BL/6 mice. Topical diacerein was observed to be safe without any adverse side effects in healthy or psoriatic animals. Our results demonstrated that diacerein significantly alleviated the psoriasiform-like skin inflammation over a 7-day period. Furthermore, diacerein significantly diminished the psoriasis-associated splenomegaly, indicating a systemic effect of the drug. Remarkably, we observed significantly reduced infiltration of CD11c dendritic cells (DCs) into the skin and spleen of psoriatic mice with diacerein treatment. As CD11c DCs play a pivotal role in psoriasis pathology, we consider diacerein to be a promising novel therapeutic candidate for psoriasis.
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These authors contributed equally to this work.
Current address: Research Program for Receptor Biochemistry and Tumor Metabolism, Department of Pediatrics, University Hospital of the Paracelsus Medical University, Muellner Hauptstr. 48, 5020 Salzburg, Austria.
Current address: Research Program for Experimental Ophthalmology and Glaucoma Research, Department of Ophthalmology and Optometry, University Hospital of the Paracelsus Medical University, 5020 Salzburg, Austria.
ISSN:1422-0067
1661-6596
1422-0067
DOI:10.3390/ijms24054324