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Comparison of topical tofacitinib and 0.1% hypochlorous acid in a murine atopic dermatitis model

BACKGROUND: Topical administration of PR022, 0.05% hypochlorous acid (HOCl) in gel has been demonstrated to be beneficial in a chronic murine atopic dermatitis model. In a follow up study we tested a higher concentration (0.1%) of PR022 HOCl gel in comparison to the Janus kinase inhibitor tofacitini...

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Autores principales: Fukuyama, Tomoki, Ehling, Sarah, Wilzopolski, Jenny, Bäumer, Wolfgang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6029395/
https://www.ncbi.nlm.nih.gov/pubmed/29970189
http://dx.doi.org/10.1186/s40360-018-0232-3
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author Fukuyama, Tomoki
Ehling, Sarah
Wilzopolski, Jenny
Bäumer, Wolfgang
author_facet Fukuyama, Tomoki
Ehling, Sarah
Wilzopolski, Jenny
Bäumer, Wolfgang
author_sort Fukuyama, Tomoki
collection PubMed
description BACKGROUND: Topical administration of PR022, 0.05% hypochlorous acid (HOCl) in gel has been demonstrated to be beneficial in a chronic murine atopic dermatitis model. In a follow up study we tested a higher concentration (0.1%) of PR022 HOCl gel in comparison to the Janus kinase inhibitor tofacitinib, both of which are currently in clinical phase studies for treatment of human atopic dermatitis. METHODS: The effect of topically administered HOCl (0.1%) in gel was compared to a topical formulation of tofacitinib (0.5%) in a therapeutic setting on atopic dermatitis-like lesions in NC/Nga mice as well as itch behaviour. NC/Nga mice were sensitized with house dust mite allergen. After reaching visible lesions, mice were treated either topically with HOCl or tofacitinib or gel vehicle for 17 days. After termination of the study, dorsal root ganglia were isolated for ex vivo stimulation and skin samples were taken for cytokine determination in inflamed skin. RESULTS: When administered onto lesional skin of NC/Nga mice, both HOCl and tofacitinib reduced lesions and scratching behaviour. The reduced inflammatory response by HOCl and tofacitinib treatment was demonstrated by diminished inflammatory cytokines in affected skin tissue from NC/Nga mice. Dorsal root ganglia neurons re-stimulated with a range of mediators of itch showed a reduced response compared to the vehicle control mice, when isolated from tofacitinib or HOCl treated mice. CONCLUSIONS: These data indicate a similar beneficial potential of topical high dose PR022 HOCl (0.1%) in gel and tofacitinib, in a translational murine model of atopic dermatitis.
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spelling pubmed-60293952018-07-09 Comparison of topical tofacitinib and 0.1% hypochlorous acid in a murine atopic dermatitis model Fukuyama, Tomoki Ehling, Sarah Wilzopolski, Jenny Bäumer, Wolfgang BMC Pharmacol Toxicol Research Article BACKGROUND: Topical administration of PR022, 0.05% hypochlorous acid (HOCl) in gel has been demonstrated to be beneficial in a chronic murine atopic dermatitis model. In a follow up study we tested a higher concentration (0.1%) of PR022 HOCl gel in comparison to the Janus kinase inhibitor tofacitinib, both of which are currently in clinical phase studies for treatment of human atopic dermatitis. METHODS: The effect of topically administered HOCl (0.1%) in gel was compared to a topical formulation of tofacitinib (0.5%) in a therapeutic setting on atopic dermatitis-like lesions in NC/Nga mice as well as itch behaviour. NC/Nga mice were sensitized with house dust mite allergen. After reaching visible lesions, mice were treated either topically with HOCl or tofacitinib or gel vehicle for 17 days. After termination of the study, dorsal root ganglia were isolated for ex vivo stimulation and skin samples were taken for cytokine determination in inflamed skin. RESULTS: When administered onto lesional skin of NC/Nga mice, both HOCl and tofacitinib reduced lesions and scratching behaviour. The reduced inflammatory response by HOCl and tofacitinib treatment was demonstrated by diminished inflammatory cytokines in affected skin tissue from NC/Nga mice. Dorsal root ganglia neurons re-stimulated with a range of mediators of itch showed a reduced response compared to the vehicle control mice, when isolated from tofacitinib or HOCl treated mice. CONCLUSIONS: These data indicate a similar beneficial potential of topical high dose PR022 HOCl (0.1%) in gel and tofacitinib, in a translational murine model of atopic dermatitis. BioMed Central 2018-07-03 /pmc/articles/PMC6029395/ /pubmed/29970189 http://dx.doi.org/10.1186/s40360-018-0232-3 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Fukuyama, Tomoki
Ehling, Sarah
Wilzopolski, Jenny
Bäumer, Wolfgang
Comparison of topical tofacitinib and 0.1% hypochlorous acid in a murine atopic dermatitis model
title Comparison of topical tofacitinib and 0.1% hypochlorous acid in a murine atopic dermatitis model
title_full Comparison of topical tofacitinib and 0.1% hypochlorous acid in a murine atopic dermatitis model
title_fullStr Comparison of topical tofacitinib and 0.1% hypochlorous acid in a murine atopic dermatitis model
title_full_unstemmed Comparison of topical tofacitinib and 0.1% hypochlorous acid in a murine atopic dermatitis model
title_short Comparison of topical tofacitinib and 0.1% hypochlorous acid in a murine atopic dermatitis model
title_sort comparison of topical tofacitinib and 0.1% hypochlorous acid in a murine atopic dermatitis model
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6029395/
https://www.ncbi.nlm.nih.gov/pubmed/29970189
http://dx.doi.org/10.1186/s40360-018-0232-3
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