TY - JOUR
T1 - Mesenchymal stromal cell therapy for acute respiratory distress syndrome due to coronavirus disease 2019
AU - Whittaker Brown, Stacey Ann
AU - Iancu-Rubin, Camelia
AU - Aboelela, Adam
AU - Abrahams, Alex
AU - Burke, Elizabeth
AU - Drummond, Tiffany
AU - Grossman, Fred
AU - Itescu, Silviu
AU - Lagdameo, Jonathan
AU - Lin, Jung Yi
AU - Mark, Alexis
AU - Levine, John E.
AU - Osman, Keren
N1 - Funding Information:
JL reports grant support and personal fees from Mesoblast Ltd and personal fees from bluebird bio and Novartis. SI, FG and EB are employees of Mesoblast Ltd. SI and FG have patents pending to Mesoblast Ltd.
Funding Information:
Remestemcel-L was provided by Mesoblast Ltd. The authors would like to thank nurse practitioners Clare Kearney, Keiko Wahlin, Ariffa Santana, Stefon Deallie, Christopher Wilkinson and Mary McLelland for administering the infusions. The authors would also like to thank Svitlana Shpontak and Yelena Sinitsyn from the Cellular Therapy Laboratory at Mount Sinai Hospital, New York, New York, USA.
Publisher Copyright:
© 2022
PY - 2022/8
Y1 - 2022/8
N2 - 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.
AB - 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.
KW - COVID-19
KW - Remestemcel-L
KW - acute respiratory distress syndrome
KW - mesenchymal stromal cells
UR - http://www.scopus.com/inward/record.url?scp=85131260603&partnerID=8YFLogxK
U2 - 10.1016/j.jcyt.2022.03.006
DO - 10.1016/j.jcyt.2022.03.006
M3 - Article
C2 - 35649958
AN - SCOPUS:85131260603
SN - 1465-3249
VL - 24
SP - 835
EP - 840
JO - Cytotherapy
JF - Cytotherapy
IS - 8
ER -