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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier Inc. on behalf of International Society for Cell & Gene Therapy. 2022
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.
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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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