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ColdZyme® protects airway epithelia from infection with BA.4/5
Vaccines against SARS-CoV-2 protect from critical or severe pathogenesis also against new variants of concern (VOCs) such as BA.4 and BA.5, but immediate interventions to avoid viral transmission and subsequent inflammatory reactions are needed. Here we applied the ColdZyme® medical device mouth spr...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9624019/ https://www.ncbi.nlm.nih.gov/pubmed/36316674 http://dx.doi.org/10.1186/s12931-022-02223-2 |
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author | Viktoria, Zaderer Stefanie, Dichtl Rosa, Bellmann-Weiler Cornelia, Lass-Flörl Wilfried, Posch Doris, Wilflingseder |
author_facet | Viktoria, Zaderer Stefanie, Dichtl Rosa, Bellmann-Weiler Cornelia, Lass-Flörl Wilfried, Posch Doris, Wilflingseder |
author_sort | Viktoria, Zaderer |
collection | PubMed |
description | Vaccines against SARS-CoV-2 protect from critical or severe pathogenesis also against new variants of concern (VOCs) such as BA.4 and BA.5, but immediate interventions to avoid viral transmission and subsequent inflammatory reactions are needed. Here we applied the ColdZyme® medical device mouth spray to fully differentiated, polarized human epithelium cultured at an air-liquid interphase (ALI). We found using VOCs BA.1 and BA.4/5 that this device effectively blocked respiratory tissue infection. While infection with these VOCs resulted in intracellular complement activation, thus enhanced inflammation, and drop of transepithelial resistance, these phenomena were prevented by a single administration of this medical device. Thus, ColdZyme® mouth spray significantly shields epithelial integrity, hinders virus infection and blocks in a secondary effect intrinsic complement activation within airway cultures also in terms of the highly contagious VOCs BA.4/5. Crucially, our in vitro data suggest that ColdZyme® mouth spray may have an impact to protect against SARS-CoV-2 transmission, also in case of the Omicron BA.1, BA.4 and BA.5 variants. |
format | Online Article Text |
id | pubmed-9624019 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-96240192022-11-02 ColdZyme® protects airway epithelia from infection with BA.4/5 Viktoria, Zaderer Stefanie, Dichtl Rosa, Bellmann-Weiler Cornelia, Lass-Flörl Wilfried, Posch Doris, Wilflingseder Respir Res Correspondence Vaccines against SARS-CoV-2 protect from critical or severe pathogenesis also against new variants of concern (VOCs) such as BA.4 and BA.5, but immediate interventions to avoid viral transmission and subsequent inflammatory reactions are needed. Here we applied the ColdZyme® medical device mouth spray to fully differentiated, polarized human epithelium cultured at an air-liquid interphase (ALI). We found using VOCs BA.1 and BA.4/5 that this device effectively blocked respiratory tissue infection. While infection with these VOCs resulted in intracellular complement activation, thus enhanced inflammation, and drop of transepithelial resistance, these phenomena were prevented by a single administration of this medical device. Thus, ColdZyme® mouth spray significantly shields epithelial integrity, hinders virus infection and blocks in a secondary effect intrinsic complement activation within airway cultures also in terms of the highly contagious VOCs BA.4/5. Crucially, our in vitro data suggest that ColdZyme® mouth spray may have an impact to protect against SARS-CoV-2 transmission, also in case of the Omicron BA.1, BA.4 and BA.5 variants. BioMed Central 2022-10-31 2022 /pmc/articles/PMC9624019/ /pubmed/36316674 http://dx.doi.org/10.1186/s12931-022-02223-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Correspondence Viktoria, Zaderer Stefanie, Dichtl Rosa, Bellmann-Weiler Cornelia, Lass-Flörl Wilfried, Posch Doris, Wilflingseder ColdZyme® protects airway epithelia from infection with BA.4/5 |
title | ColdZyme® protects airway epithelia from infection with BA.4/5 |
title_full | ColdZyme® protects airway epithelia from infection with BA.4/5 |
title_fullStr | ColdZyme® protects airway epithelia from infection with BA.4/5 |
title_full_unstemmed | ColdZyme® protects airway epithelia from infection with BA.4/5 |
title_short | ColdZyme® protects airway epithelia from infection with BA.4/5 |
title_sort | coldzyme® protects airway epithelia from infection with ba.4/5 |
topic | Correspondence |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9624019/ https://www.ncbi.nlm.nih.gov/pubmed/36316674 http://dx.doi.org/10.1186/s12931-022-02223-2 |
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