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Cellular benefits of single‐use negative pressure wound therapy demonstrated in a novel ex vivo human skin wound model

Negative pressure wound therapy is a widely used treatment for chronic, nonhealing wounds. Surprisingly, few studies have systematically evaluated the cellular and molecular effects of negative pressure treatment on human skin. In addition, no study to date has directly compared recently available s...

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Autores principales: Wilkinson, Holly N., Longhorne, Francesca L., Roberts, Elizabeth R., Brownhill, Varuni R., Hardman, Matthew J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9291807/
https://www.ncbi.nlm.nih.gov/pubmed/33378127
http://dx.doi.org/10.1111/wrr.12888
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author Wilkinson, Holly N.
Longhorne, Francesca L.
Roberts, Elizabeth R.
Brownhill, Varuni R.
Hardman, Matthew J.
author_facet Wilkinson, Holly N.
Longhorne, Francesca L.
Roberts, Elizabeth R.
Brownhill, Varuni R.
Hardman, Matthew J.
author_sort Wilkinson, Holly N.
collection PubMed
description Negative pressure wound therapy is a widely used treatment for chronic, nonhealing wounds. Surprisingly, few studies have systematically evaluated the cellular and molecular effects of negative pressure treatment on human skin. In addition, no study to date has directly compared recently available single‐use negative pressure modalities to traditional negative pressure devices in a controlled setting. Here we developed a novel large‐scale ex vivo human skin culture system to effectively evaluate the efficacy of two different negative pressure wound therapy modalities. Single‐use and traditional negative pressure devices were applied to human ex vivo wounded skin sheets cultured over a period of 48 hours. Cellular tissue response to therapy was evaluated via a combination of histological analysis and transcriptional profiling, in samples collected from the wound edge, skin adjacent to the wound, and an extended skin region. Single‐use negative pressure wound therapy caused less damage to wound edge tissue than traditional application, demonstrated by improved skin barrier, reduced dermal‐epidermal junction disruption and a dampened damage response. Transcriptional profiling confirmed significantly less activation of multiple pro‐inflammatory markers in wound edge skin treated with single‐use vs traditional negative pressure therapy. These findings may help to explain the greater efficacy of sNPWT in the clinic, while offering a noninvasive system to develop improved NPWT‐based therapies.
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spelling pubmed-92918072022-07-20 Cellular benefits of single‐use negative pressure wound therapy demonstrated in a novel ex vivo human skin wound model Wilkinson, Holly N. Longhorne, Francesca L. Roberts, Elizabeth R. Brownhill, Varuni R. Hardman, Matthew J. Wound Repair Regen Original Research‐Basic Science Negative pressure wound therapy is a widely used treatment for chronic, nonhealing wounds. Surprisingly, few studies have systematically evaluated the cellular and molecular effects of negative pressure treatment on human skin. In addition, no study to date has directly compared recently available single‐use negative pressure modalities to traditional negative pressure devices in a controlled setting. Here we developed a novel large‐scale ex vivo human skin culture system to effectively evaluate the efficacy of two different negative pressure wound therapy modalities. Single‐use and traditional negative pressure devices were applied to human ex vivo wounded skin sheets cultured over a period of 48 hours. Cellular tissue response to therapy was evaluated via a combination of histological analysis and transcriptional profiling, in samples collected from the wound edge, skin adjacent to the wound, and an extended skin region. Single‐use negative pressure wound therapy caused less damage to wound edge tissue than traditional application, demonstrated by improved skin barrier, reduced dermal‐epidermal junction disruption and a dampened damage response. Transcriptional profiling confirmed significantly less activation of multiple pro‐inflammatory markers in wound edge skin treated with single‐use vs traditional negative pressure therapy. These findings may help to explain the greater efficacy of sNPWT in the clinic, while offering a noninvasive system to develop improved NPWT‐based therapies. John Wiley & Sons, Inc. 2020-12-30 2021 /pmc/articles/PMC9291807/ /pubmed/33378127 http://dx.doi.org/10.1111/wrr.12888 Text en © 2020 The Authors. Wound Repair and Regeneration published by Wiley Periodicals LLC on behalf of The Wound Healing Society. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Research‐Basic Science
Wilkinson, Holly N.
Longhorne, Francesca L.
Roberts, Elizabeth R.
Brownhill, Varuni R.
Hardman, Matthew J.
Cellular benefits of single‐use negative pressure wound therapy demonstrated in a novel ex vivo human skin wound model
title Cellular benefits of single‐use negative pressure wound therapy demonstrated in a novel ex vivo human skin wound model
title_full Cellular benefits of single‐use negative pressure wound therapy demonstrated in a novel ex vivo human skin wound model
title_fullStr Cellular benefits of single‐use negative pressure wound therapy demonstrated in a novel ex vivo human skin wound model
title_full_unstemmed Cellular benefits of single‐use negative pressure wound therapy demonstrated in a novel ex vivo human skin wound model
title_short Cellular benefits of single‐use negative pressure wound therapy demonstrated in a novel ex vivo human skin wound model
title_sort cellular benefits of single‐use negative pressure wound therapy demonstrated in a novel ex vivo human skin wound model
topic Original Research‐Basic Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9291807/
https://www.ncbi.nlm.nih.gov/pubmed/33378127
http://dx.doi.org/10.1111/wrr.12888
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