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Time-Dependent Molecular Motifs of Pulmonary Fibrogenesis in COVID-19

(1) Background: In COVID-19 survivors there is an increased prevalence of pulmonary fibrosis of which the underlying molecular mechanisms are poorly understood; (2) Methods: In this multicentric study, n = 12 patients who succumbed to COVID-19 due to progressive respiratory failure were assigned to...

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Autores principales: Kamp, Jan C., Neubert, Lavinia, Ackermann, Maximilian, Stark, Helge, Werlein, Christopher, Fuge, Jan, Haverich, Axel, Tzankov, Alexandar, Steinestel, Konrad, Friemann, Johannes, Boor, Peter, Junker, Klaus, Hoeper, Marius M., Welte, Tobias, Laenger, Florian, Kuehnel, Mark P., Jonigk, Danny D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8835897/
https://www.ncbi.nlm.nih.gov/pubmed/35163504
http://dx.doi.org/10.3390/ijms23031583
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author Kamp, Jan C.
Neubert, Lavinia
Ackermann, Maximilian
Stark, Helge
Werlein, Christopher
Fuge, Jan
Haverich, Axel
Tzankov, Alexandar
Steinestel, Konrad
Friemann, Johannes
Boor, Peter
Junker, Klaus
Hoeper, Marius M.
Welte, Tobias
Laenger, Florian
Kuehnel, Mark P.
Jonigk, Danny D.
author_facet Kamp, Jan C.
Neubert, Lavinia
Ackermann, Maximilian
Stark, Helge
Werlein, Christopher
Fuge, Jan
Haverich, Axel
Tzankov, Alexandar
Steinestel, Konrad
Friemann, Johannes
Boor, Peter
Junker, Klaus
Hoeper, Marius M.
Welte, Tobias
Laenger, Florian
Kuehnel, Mark P.
Jonigk, Danny D.
author_sort Kamp, Jan C.
collection PubMed
description (1) Background: In COVID-19 survivors there is an increased prevalence of pulmonary fibrosis of which the underlying molecular mechanisms are poorly understood; (2) Methods: In this multicentric study, n = 12 patients who succumbed to COVID-19 due to progressive respiratory failure were assigned to an early and late group (death within ≤7 and >7 days of hospitalization, respectively) and compared to n = 11 healthy controls; mRNA and protein expression as well as biological pathway analysis were performed to gain insights into the evolution of pulmonary fibrogenesis in COVID-19; (3) Results: Median duration of hospitalization until death was 3 (IQR25-75, 3–3.75) and 14 (12.5–14) days in the early and late group, respectively. Fifty-eight out of 770 analyzed genes showed a significantly altered expression signature in COVID-19 compared to controls in a time-dependent manner. The entire study group showed an increased expression of BST2 and IL1R1, independent of hospitalization time. In the early group there was increased activity of inflammation-related genes and pathways, while fibrosis-related genes (particularly PDGFRB) and pathways dominated in the late group; (4) Conclusions: After the first week of hospitalization, there is a shift from pro-inflammatory to fibrogenic activity in severe COVID-19. IL1R1 and PDGFRB may serve as potential therapeutic targets in future studies.
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spelling pubmed-88358972022-02-12 Time-Dependent Molecular Motifs of Pulmonary Fibrogenesis in COVID-19 Kamp, Jan C. Neubert, Lavinia Ackermann, Maximilian Stark, Helge Werlein, Christopher Fuge, Jan Haverich, Axel Tzankov, Alexandar Steinestel, Konrad Friemann, Johannes Boor, Peter Junker, Klaus Hoeper, Marius M. Welte, Tobias Laenger, Florian Kuehnel, Mark P. Jonigk, Danny D. Int J Mol Sci Article (1) Background: In COVID-19 survivors there is an increased prevalence of pulmonary fibrosis of which the underlying molecular mechanisms are poorly understood; (2) Methods: In this multicentric study, n = 12 patients who succumbed to COVID-19 due to progressive respiratory failure were assigned to an early and late group (death within ≤7 and >7 days of hospitalization, respectively) and compared to n = 11 healthy controls; mRNA and protein expression as well as biological pathway analysis were performed to gain insights into the evolution of pulmonary fibrogenesis in COVID-19; (3) Results: Median duration of hospitalization until death was 3 (IQR25-75, 3–3.75) and 14 (12.5–14) days in the early and late group, respectively. Fifty-eight out of 770 analyzed genes showed a significantly altered expression signature in COVID-19 compared to controls in a time-dependent manner. The entire study group showed an increased expression of BST2 and IL1R1, independent of hospitalization time. In the early group there was increased activity of inflammation-related genes and pathways, while fibrosis-related genes (particularly PDGFRB) and pathways dominated in the late group; (4) Conclusions: After the first week of hospitalization, there is a shift from pro-inflammatory to fibrogenic activity in severe COVID-19. IL1R1 and PDGFRB may serve as potential therapeutic targets in future studies. MDPI 2022-01-29 /pmc/articles/PMC8835897/ /pubmed/35163504 http://dx.doi.org/10.3390/ijms23031583 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kamp, Jan C.
Neubert, Lavinia
Ackermann, Maximilian
Stark, Helge
Werlein, Christopher
Fuge, Jan
Haverich, Axel
Tzankov, Alexandar
Steinestel, Konrad
Friemann, Johannes
Boor, Peter
Junker, Klaus
Hoeper, Marius M.
Welte, Tobias
Laenger, Florian
Kuehnel, Mark P.
Jonigk, Danny D.
Time-Dependent Molecular Motifs of Pulmonary Fibrogenesis in COVID-19
title Time-Dependent Molecular Motifs of Pulmonary Fibrogenesis in COVID-19
title_full Time-Dependent Molecular Motifs of Pulmonary Fibrogenesis in COVID-19
title_fullStr Time-Dependent Molecular Motifs of Pulmonary Fibrogenesis in COVID-19
title_full_unstemmed Time-Dependent Molecular Motifs of Pulmonary Fibrogenesis in COVID-19
title_short Time-Dependent Molecular Motifs of Pulmonary Fibrogenesis in COVID-19
title_sort time-dependent molecular motifs of pulmonary fibrogenesis in covid-19
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8835897/
https://www.ncbi.nlm.nih.gov/pubmed/35163504
http://dx.doi.org/10.3390/ijms23031583
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