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Mesenchymal stromal cell therapy for acute respiratory distress syndrome due to coronavirus disease 2019
BACKGROUND AIMS: The acute respiratory distress syndrome (ARDS) resulting from coronavirus disease 2019 (COVID-19) is associated with a massive release of inflammatory cytokines and high mortality. Mesenchymal stromal cells (MSCs) have anti-inflammatory properties and have shown activity in treating...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Published by Elsevier Inc. on behalf of International Society for Cell & Gene Therapy.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8995321/ https://www.ncbi.nlm.nih.gov/pubmed/35649958 http://dx.doi.org/10.1016/j.jcyt.2022.03.006 |
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author | Whittaker Brown, Stacey-Ann Iancu-Rubin, Camelia Aboelela, Adam Abrahams, Alex Burke, Elizabeth Drummond, Tiffany Grossman, Fred Itescu, Silviu Lagdameo, Jonathan Lin, Jung-Yi Mark, Alexis Levine, John E. Osman, Keren |
author_facet | Whittaker Brown, Stacey-Ann Iancu-Rubin, Camelia Aboelela, Adam Abrahams, Alex Burke, Elizabeth Drummond, Tiffany Grossman, Fred Itescu, Silviu Lagdameo, Jonathan Lin, Jung-Yi Mark, Alexis Levine, John E. Osman, Keren |
author_sort | Whittaker Brown, Stacey-Ann |
collection | PubMed |
description | BACKGROUND AIMS: The acute respiratory distress syndrome (ARDS) resulting from coronavirus disease 2019 (COVID-19) is associated with a massive release of inflammatory cytokines and high mortality. Mesenchymal stromal cells (MSCs) have anti-inflammatory properties and have shown activity in treating acute lung injury. Here the authors report a case series of 11 patients with COVID-19-associated ARDS (CARDS) requiring mechanical ventilation who were treated with remestemcel-L, an allogeneic MSC product, under individual patient emergency investigational new drug applications. METHODS: Patients were eligible if they were mechanically ventilated for less than 72 h prior to the first infusion. Patients with pre-existing lung disease requiring supplemental oxygen or severe liver or kidney injury were excluded. Each patient received two infusions of remestemcel-L at a dose of 2 million cells/kg per infusion given 48–120 h apart. RESULTS: Remestemcel-L infusions were well tolerated in all 11 patients. At the end of the 28-day follow-up period, 10 (91%, 95% confidence interval [CI], 59–100%) patients were extubated, nine (82%, 95% CI, 48–97%) patients remained liberated from mechanical ventilation and were discharged from the intensive care unit and two (18%, 95 CI%, 2–52%) patients died. The median time to extubation was 10 days. Eight (73%, 95% CI, 34–100%) patients were discharged from the hospital. C-reactive protein levels significantly declined within 5 days of MSC infusion. CONCLUSIONS: The authors demonstrate in this case series that remestemcel-L infusions to treat moderate to severe CARDS were safe and well tolerated and resulted in improved clinical outcomes. |
format | Online Article Text |
id | pubmed-8995321 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Published by Elsevier Inc. on behalf of International Society for Cell & Gene Therapy. |
record_format | MEDLINE/PubMed |
spelling | pubmed-89953212022-04-11 Mesenchymal stromal cell therapy for acute respiratory distress syndrome due to coronavirus disease 2019 Whittaker Brown, Stacey-Ann Iancu-Rubin, Camelia Aboelela, Adam Abrahams, Alex Burke, Elizabeth Drummond, Tiffany Grossman, Fred Itescu, Silviu Lagdameo, Jonathan Lin, Jung-Yi Mark, Alexis Levine, John E. Osman, Keren Cytotherapy Full-Length Article BACKGROUND AIMS: The acute respiratory distress syndrome (ARDS) resulting from coronavirus disease 2019 (COVID-19) is associated with a massive release of inflammatory cytokines and high mortality. Mesenchymal stromal cells (MSCs) have anti-inflammatory properties and have shown activity in treating acute lung injury. Here the authors report a case series of 11 patients with COVID-19-associated ARDS (CARDS) requiring mechanical ventilation who were treated with remestemcel-L, an allogeneic MSC product, under individual patient emergency investigational new drug applications. METHODS: Patients were eligible if they were mechanically ventilated for less than 72 h prior to the first infusion. Patients with pre-existing lung disease requiring supplemental oxygen or severe liver or kidney injury were excluded. Each patient received two infusions of remestemcel-L at a dose of 2 million cells/kg per infusion given 48–120 h apart. RESULTS: Remestemcel-L infusions were well tolerated in all 11 patients. At the end of the 28-day follow-up period, 10 (91%, 95% confidence interval [CI], 59–100%) patients were extubated, nine (82%, 95% CI, 48–97%) patients remained liberated from mechanical ventilation and were discharged from the intensive care unit and two (18%, 95 CI%, 2–52%) patients died. The median time to extubation was 10 days. Eight (73%, 95% CI, 34–100%) patients were discharged from the hospital. C-reactive protein levels significantly declined within 5 days of MSC infusion. CONCLUSIONS: The authors demonstrate in this case series that remestemcel-L infusions to treat moderate to severe CARDS were safe and well tolerated and resulted in improved clinical outcomes. Published by Elsevier Inc. on behalf of International Society for Cell & Gene Therapy. 2022-08 2022-04-11 /pmc/articles/PMC8995321/ /pubmed/35649958 http://dx.doi.org/10.1016/j.jcyt.2022.03.006 Text en © 2022 Published by Elsevier Inc. on behalf of International Society for Cell & Gene Therapy. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Full-Length Article Whittaker Brown, Stacey-Ann Iancu-Rubin, Camelia Aboelela, Adam Abrahams, Alex Burke, Elizabeth Drummond, Tiffany Grossman, Fred Itescu, Silviu Lagdameo, Jonathan Lin, Jung-Yi Mark, Alexis Levine, John E. Osman, Keren Mesenchymal stromal cell therapy for acute respiratory distress syndrome due to coronavirus disease 2019 |
title | Mesenchymal stromal cell therapy for acute respiratory distress syndrome due to coronavirus disease 2019 |
title_full | Mesenchymal stromal cell therapy for acute respiratory distress syndrome due to coronavirus disease 2019 |
title_fullStr | Mesenchymal stromal cell therapy for acute respiratory distress syndrome due to coronavirus disease 2019 |
title_full_unstemmed | Mesenchymal stromal cell therapy for acute respiratory distress syndrome due to coronavirus disease 2019 |
title_short | Mesenchymal stromal cell therapy for acute respiratory distress syndrome due to coronavirus disease 2019 |
title_sort | mesenchymal stromal cell therapy for acute respiratory distress syndrome due to coronavirus disease 2019 |
topic | Full-Length Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8995321/ https://www.ncbi.nlm.nih.gov/pubmed/35649958 http://dx.doi.org/10.1016/j.jcyt.2022.03.006 |
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