Cargando…

Lung Surfactant Accelerates Skin Wound Healing: A Translational Study with a Randomized Clinical Phase I Study

Lung surfactants are used for reducing alveolar surface tension in preterm infants to ease breathing. Phospholipid films with surfactant proteins regulate the activity of alveolar macrophages and reduce inflammation. Aberrant skin wound healing is characterized by persistent inflammation. The aim of...

Descripción completa

Detalles Bibliográficos
Autores principales: Mirastschijski, Ursula, Schwab, Igor, Coger, Vincent, Zier, Ulrich, Rianna, Carmela, He, Wei, Maedler, Kathrin, Kelm, Sørge, Radtke, Arlo, Belge, Gazanfer, Lindner, Patrick, Stahl, Frank, Scharpenberg, Martin, Lasota, Lukas, Timm, Jürgen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7018835/
https://www.ncbi.nlm.nih.gov/pubmed/32054903
http://dx.doi.org/10.1038/s41598-020-59394-5
_version_ 1783497404942647296
author Mirastschijski, Ursula
Schwab, Igor
Coger, Vincent
Zier, Ulrich
Rianna, Carmela
He, Wei
Maedler, Kathrin
Kelm, Sørge
Radtke, Arlo
Belge, Gazanfer
Lindner, Patrick
Stahl, Frank
Scharpenberg, Martin
Lasota, Lukas
Timm, Jürgen
author_facet Mirastschijski, Ursula
Schwab, Igor
Coger, Vincent
Zier, Ulrich
Rianna, Carmela
He, Wei
Maedler, Kathrin
Kelm, Sørge
Radtke, Arlo
Belge, Gazanfer
Lindner, Patrick
Stahl, Frank
Scharpenberg, Martin
Lasota, Lukas
Timm, Jürgen
author_sort Mirastschijski, Ursula
collection PubMed
description Lung surfactants are used for reducing alveolar surface tension in preterm infants to ease breathing. Phospholipid films with surfactant proteins regulate the activity of alveolar macrophages and reduce inflammation. Aberrant skin wound healing is characterized by persistent inflammation. The aim of the study was to investigate if lung surfactant can promote wound healing. Preclinical wound models, e.g. cell scratch assays and full-thickness excisional wounds in mice, and a randomized, phase I clinical trial in healthy human volunteers using a suction blister model were used to study the effect of the commercially available bovine lung surfactant on skin wound repair. Lung surfactant increased migration of keratinocytes in a concentration-dependent manner with no effect on fibroblasts. Significantly reduced expression levels were found for pro-inflammatory and pro-fibrotic genes in murine wounds. Because of these beneficial effects in preclinical experiments, a clinical phase I study was initiated to monitor safety and tolerability of surfactant when applied topically onto human wounds and normal skin. No adverse effects were observed. Subepidermal wounds healed significantly faster with surfactant compared to control. Our study provides lung surfactant as a strong candidate for innovative treatment of chronic skin wounds and as additive for treatment of burn wounds to reduce inflammation and prevent excessive scarring.
format Online
Article
Text
id pubmed-7018835
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-70188352020-02-21 Lung Surfactant Accelerates Skin Wound Healing: A Translational Study with a Randomized Clinical Phase I Study Mirastschijski, Ursula Schwab, Igor Coger, Vincent Zier, Ulrich Rianna, Carmela He, Wei Maedler, Kathrin Kelm, Sørge Radtke, Arlo Belge, Gazanfer Lindner, Patrick Stahl, Frank Scharpenberg, Martin Lasota, Lukas Timm, Jürgen Sci Rep Article Lung surfactants are used for reducing alveolar surface tension in preterm infants to ease breathing. Phospholipid films with surfactant proteins regulate the activity of alveolar macrophages and reduce inflammation. Aberrant skin wound healing is characterized by persistent inflammation. The aim of the study was to investigate if lung surfactant can promote wound healing. Preclinical wound models, e.g. cell scratch assays and full-thickness excisional wounds in mice, and a randomized, phase I clinical trial in healthy human volunteers using a suction blister model were used to study the effect of the commercially available bovine lung surfactant on skin wound repair. Lung surfactant increased migration of keratinocytes in a concentration-dependent manner with no effect on fibroblasts. Significantly reduced expression levels were found for pro-inflammatory and pro-fibrotic genes in murine wounds. Because of these beneficial effects in preclinical experiments, a clinical phase I study was initiated to monitor safety and tolerability of surfactant when applied topically onto human wounds and normal skin. No adverse effects were observed. Subepidermal wounds healed significantly faster with surfactant compared to control. Our study provides lung surfactant as a strong candidate for innovative treatment of chronic skin wounds and as additive for treatment of burn wounds to reduce inflammation and prevent excessive scarring. Nature Publishing Group UK 2020-02-13 /pmc/articles/PMC7018835/ /pubmed/32054903 http://dx.doi.org/10.1038/s41598-020-59394-5 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Mirastschijski, Ursula
Schwab, Igor
Coger, Vincent
Zier, Ulrich
Rianna, Carmela
He, Wei
Maedler, Kathrin
Kelm, Sørge
Radtke, Arlo
Belge, Gazanfer
Lindner, Patrick
Stahl, Frank
Scharpenberg, Martin
Lasota, Lukas
Timm, Jürgen
Lung Surfactant Accelerates Skin Wound Healing: A Translational Study with a Randomized Clinical Phase I Study
title Lung Surfactant Accelerates Skin Wound Healing: A Translational Study with a Randomized Clinical Phase I Study
title_full Lung Surfactant Accelerates Skin Wound Healing: A Translational Study with a Randomized Clinical Phase I Study
title_fullStr Lung Surfactant Accelerates Skin Wound Healing: A Translational Study with a Randomized Clinical Phase I Study
title_full_unstemmed Lung Surfactant Accelerates Skin Wound Healing: A Translational Study with a Randomized Clinical Phase I Study
title_short Lung Surfactant Accelerates Skin Wound Healing: A Translational Study with a Randomized Clinical Phase I Study
title_sort lung surfactant accelerates skin wound healing: a translational study with a randomized clinical phase i study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7018835/
https://www.ncbi.nlm.nih.gov/pubmed/32054903
http://dx.doi.org/10.1038/s41598-020-59394-5
work_keys_str_mv AT mirastschijskiursula lungsurfactantacceleratesskinwoundhealingatranslationalstudywitharandomizedclinicalphaseistudy
AT schwabigor lungsurfactantacceleratesskinwoundhealingatranslationalstudywitharandomizedclinicalphaseistudy
AT cogervincent lungsurfactantacceleratesskinwoundhealingatranslationalstudywitharandomizedclinicalphaseistudy
AT zierulrich lungsurfactantacceleratesskinwoundhealingatranslationalstudywitharandomizedclinicalphaseistudy
AT riannacarmela lungsurfactantacceleratesskinwoundhealingatranslationalstudywitharandomizedclinicalphaseistudy
AT hewei lungsurfactantacceleratesskinwoundhealingatranslationalstudywitharandomizedclinicalphaseistudy
AT maedlerkathrin lungsurfactantacceleratesskinwoundhealingatranslationalstudywitharandomizedclinicalphaseistudy
AT kelmsørge lungsurfactantacceleratesskinwoundhealingatranslationalstudywitharandomizedclinicalphaseistudy
AT radtkearlo lungsurfactantacceleratesskinwoundhealingatranslationalstudywitharandomizedclinicalphaseistudy
AT belgegazanfer lungsurfactantacceleratesskinwoundhealingatranslationalstudywitharandomizedclinicalphaseistudy
AT lindnerpatrick lungsurfactantacceleratesskinwoundhealingatranslationalstudywitharandomizedclinicalphaseistudy
AT stahlfrank lungsurfactantacceleratesskinwoundhealingatranslationalstudywitharandomizedclinicalphaseistudy
AT scharpenbergmartin lungsurfactantacceleratesskinwoundhealingatranslationalstudywitharandomizedclinicalphaseistudy
AT lasotalukas lungsurfactantacceleratesskinwoundhealingatranslationalstudywitharandomizedclinicalphaseistudy
AT timmjurgen lungsurfactantacceleratesskinwoundhealingatranslationalstudywitharandomizedclinicalphaseistudy