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Mechanism of Oleogel‐S10: A triterpene preparation for the treatment of epidermolysis bullosa
Epidermolysis bullosa (EB) is a group of rare heterogeneous, genetic disorders. Currently, there is no effective pharmacological or genetic therapy for all EB subtypes. Dry extract from birch bark and betulin upregulate some pro‐inflammatory mediators and downregulate others. The increase in pro‐inf...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6771815/ https://www.ncbi.nlm.nih.gov/pubmed/31168940 http://dx.doi.org/10.1111/dth.12983 |
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author | Schwieger‐Briel, Agnes Ott, Hagen Kiritsi, Dimitra Laszczyk‐Lauer, Melanie Bodemer, Christine |
author_facet | Schwieger‐Briel, Agnes Ott, Hagen Kiritsi, Dimitra Laszczyk‐Lauer, Melanie Bodemer, Christine |
author_sort | Schwieger‐Briel, Agnes |
collection | PubMed |
description | Epidermolysis bullosa (EB) is a group of rare heterogeneous, genetic disorders. Currently, there is no effective pharmacological or genetic therapy for all EB subtypes. Dry extract from birch bark and betulin upregulate some pro‐inflammatory mediators and downregulate others. The increase in pro‐inflammatory cytokines is temporary and attenuated over long‐term treatment. This inflammatory stimulus is thought to be prerequisite for a secondary anti‐inflammatory response. Dry extract from birch bark and its active marker substances have also been shown to increase the migration of primary human keratinocytes, accelerate wound closure, and promote differentiation of keratinocytes in vitro and in vivo—processes that are essential for reepithelialization and maintenance of the skin barrier. Comprehensive clinical data are available to support the use of Oleogel‐S10 in the treatment of partial thickness wounds of different etiologies, and a proof‐of‐concept Phase 2 study in patients with dystrophic EB has suggested the potential for faster reepithelialization of wounds treated with Oleogel‐S10. |
format | Online Article Text |
id | pubmed-6771815 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-67718152019-10-07 Mechanism of Oleogel‐S10: A triterpene preparation for the treatment of epidermolysis bullosa Schwieger‐Briel, Agnes Ott, Hagen Kiritsi, Dimitra Laszczyk‐Lauer, Melanie Bodemer, Christine Dermatol Ther Review Articles Epidermolysis bullosa (EB) is a group of rare heterogeneous, genetic disorders. Currently, there is no effective pharmacological or genetic therapy for all EB subtypes. Dry extract from birch bark and betulin upregulate some pro‐inflammatory mediators and downregulate others. The increase in pro‐inflammatory cytokines is temporary and attenuated over long‐term treatment. This inflammatory stimulus is thought to be prerequisite for a secondary anti‐inflammatory response. Dry extract from birch bark and its active marker substances have also been shown to increase the migration of primary human keratinocytes, accelerate wound closure, and promote differentiation of keratinocytes in vitro and in vivo—processes that are essential for reepithelialization and maintenance of the skin barrier. Comprehensive clinical data are available to support the use of Oleogel‐S10 in the treatment of partial thickness wounds of different etiologies, and a proof‐of‐concept Phase 2 study in patients with dystrophic EB has suggested the potential for faster reepithelialization of wounds treated with Oleogel‐S10. John Wiley & Sons, Inc. 2019-07-02 2019 /pmc/articles/PMC6771815/ /pubmed/31168940 http://dx.doi.org/10.1111/dth.12983 Text en © 2019 The Authors. Dermatologic Therapy published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Articles Schwieger‐Briel, Agnes Ott, Hagen Kiritsi, Dimitra Laszczyk‐Lauer, Melanie Bodemer, Christine Mechanism of Oleogel‐S10: A triterpene preparation for the treatment of epidermolysis bullosa |
title | Mechanism of Oleogel‐S10: A triterpene preparation for the treatment of epidermolysis bullosa |
title_full | Mechanism of Oleogel‐S10: A triterpene preparation for the treatment of epidermolysis bullosa |
title_fullStr | Mechanism of Oleogel‐S10: A triterpene preparation for the treatment of epidermolysis bullosa |
title_full_unstemmed | Mechanism of Oleogel‐S10: A triterpene preparation for the treatment of epidermolysis bullosa |
title_short | Mechanism of Oleogel‐S10: A triterpene preparation for the treatment of epidermolysis bullosa |
title_sort | mechanism of oleogel‐s10: a triterpene preparation for the treatment of epidermolysis bullosa |
topic | Review Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6771815/ https://www.ncbi.nlm.nih.gov/pubmed/31168940 http://dx.doi.org/10.1111/dth.12983 |
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