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Mesenchymal Stem Cell Therapy for Severe COVID-19 ARDS
BACKGROUND: The COVID-19 pandemic reached Germany in spring 2020. No proven treatment for SARS-CoV-2 was available at that time, especially for severe COVID-19-induced ARDS. We determined whether the infusion of mesenchymal stromal cells (MSCs) would help to improve pulmonary function and overall ou...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8145440/ https://www.ncbi.nlm.nih.gov/pubmed/33663244 http://dx.doi.org/10.1177/0885066621997365 |
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author | Häberle, Helene Magunia, Harry Lang, Peter Gloeckner, Henning Körner, Andreas Koeppen, Michael Backchoul, Tamam Malek, Nisar Handgretinger, Rupert Rosenberger, Peter Mirakaj, Valbona |
author_facet | Häberle, Helene Magunia, Harry Lang, Peter Gloeckner, Henning Körner, Andreas Koeppen, Michael Backchoul, Tamam Malek, Nisar Handgretinger, Rupert Rosenberger, Peter Mirakaj, Valbona |
author_sort | Häberle, Helene |
collection | PubMed |
description | BACKGROUND: The COVID-19 pandemic reached Germany in spring 2020. No proven treatment for SARS-CoV-2 was available at that time, especially for severe COVID-19-induced ARDS. We determined whether the infusion of mesenchymal stromal cells (MSCs) would help to improve pulmonary function and overall outcome in patients with severe COVID-19 ARDS. We offered MSC infusion as an extended indication to all critically ill COVID-19 patients with a Horovitz index <100. We treated 5 out of 23 patients with severe COVID-19 ARDS with an infusion of MSCs. One million MSCs/kg body weight was infused over 30 minutes, and the process was repeated in 3 patients twice and in 2 patients 3 times. RESULT: Four out of 5 MSC-treated patients compared to 50% of control patients (9 out of 18) received ECMO support (80%). The MSC group showed a higher Murray score on admission than control patients, reflecting more severe pulmonary compromise (3.5 ± 0.2 versus 2.8 ± 0.3). MSC infusion was safe and well tolerated. The MSC group had a significantly higher Horovitz score on discharge than the control group. Compared to controls, patients with MSC treatment showed a significantly lower Murray score upon discharge than controls. In the MSC group, 4 out of 5 patients (80%) survived to discharge and exhibited good pulmonary function, whereas only 8 out of 18 patients (45%) in the control group survived to discharge. CONCLUSION: MSC infusion is a safe treatment for COVID-19 ARDS that improves pulmonary function and overall outcome in this patient population. |
format | Online Article Text |
id | pubmed-8145440 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-81454402021-06-07 Mesenchymal Stem Cell Therapy for Severe COVID-19 ARDS Häberle, Helene Magunia, Harry Lang, Peter Gloeckner, Henning Körner, Andreas Koeppen, Michael Backchoul, Tamam Malek, Nisar Handgretinger, Rupert Rosenberger, Peter Mirakaj, Valbona J Intensive Care Med Original Research BACKGROUND: The COVID-19 pandemic reached Germany in spring 2020. No proven treatment for SARS-CoV-2 was available at that time, especially for severe COVID-19-induced ARDS. We determined whether the infusion of mesenchymal stromal cells (MSCs) would help to improve pulmonary function and overall outcome in patients with severe COVID-19 ARDS. We offered MSC infusion as an extended indication to all critically ill COVID-19 patients with a Horovitz index <100. We treated 5 out of 23 patients with severe COVID-19 ARDS with an infusion of MSCs. One million MSCs/kg body weight was infused over 30 minutes, and the process was repeated in 3 patients twice and in 2 patients 3 times. RESULT: Four out of 5 MSC-treated patients compared to 50% of control patients (9 out of 18) received ECMO support (80%). The MSC group showed a higher Murray score on admission than control patients, reflecting more severe pulmonary compromise (3.5 ± 0.2 versus 2.8 ± 0.3). MSC infusion was safe and well tolerated. The MSC group had a significantly higher Horovitz score on discharge than the control group. Compared to controls, patients with MSC treatment showed a significantly lower Murray score upon discharge than controls. In the MSC group, 4 out of 5 patients (80%) survived to discharge and exhibited good pulmonary function, whereas only 8 out of 18 patients (45%) in the control group survived to discharge. CONCLUSION: MSC infusion is a safe treatment for COVID-19 ARDS that improves pulmonary function and overall outcome in this patient population. SAGE Publications 2021-03-05 2021-06 /pmc/articles/PMC8145440/ /pubmed/33663244 http://dx.doi.org/10.1177/0885066621997365 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Research Häberle, Helene Magunia, Harry Lang, Peter Gloeckner, Henning Körner, Andreas Koeppen, Michael Backchoul, Tamam Malek, Nisar Handgretinger, Rupert Rosenberger, Peter Mirakaj, Valbona Mesenchymal Stem Cell Therapy for Severe COVID-19 ARDS |
title | Mesenchymal Stem Cell Therapy for Severe COVID-19 ARDS |
title_full | Mesenchymal Stem Cell Therapy for Severe COVID-19 ARDS |
title_fullStr | Mesenchymal Stem Cell Therapy for Severe COVID-19 ARDS |
title_full_unstemmed | Mesenchymal Stem Cell Therapy for Severe COVID-19 ARDS |
title_short | Mesenchymal Stem Cell Therapy for Severe COVID-19 ARDS |
title_sort | mesenchymal stem cell therapy for severe covid-19 ards |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8145440/ https://www.ncbi.nlm.nih.gov/pubmed/33663244 http://dx.doi.org/10.1177/0885066621997365 |
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