Cellular immunotherapy for COVID-19-induced acute respiratory distress syndrome: Results of the CIRCA-19 phase 1 safety and phase 2 randomized controlled trials

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Shane W. English - , Ottawa Hospital Research Institute, University of Ottawa (Author)
  • Dean A. Fergusson - , Ottawa Hospital Research Institute, University of Ottawa (Author)
  • Manoj Mathew Lalu - , Ottawa Hospital Research Institute, University of Ottawa (Author)
  • David W. Courtman - , Ottawa Hospital Research Institute (Author)
  • Saad Khan - , Ottawa Hospital Research Institute (Author)
  • Mohamad Sobh - , Ottawa Hospital Research Institute (Author)
  • Irene Watpool - , Ottawa Hospital Research Institute (Author)
  • Josee Champagne - , Ottawa Hospital Research Institute (Author)
  • Samantha Hodgins - , Ottawa Hospital Research Institute (Author)
  • Bernard Thébaud - , Ottawa Hospital Research Institute, University of Ottawa (Author)
  • Karim Soliman - , Lakeridge Health Corporation, Queen's University Kingston (Author)
  • Michaël Chassé - , University of Montreal (Author)
  • Claudia C. dos Santos - , University of Toronto (Author)
  • Marius A. Möbius - , GMP Facility, Center for feto/neonatal Health (Author)
  • Daniel Freund - , GMP Facility, Center for feto/neonatal Health (Author)
  • Mario Rüdiger - , Center for feto/neonatal Health (Author)
  • Duncan J. Stewart - , University of Ottawa, Ottawa Hospital Research Institute (Author)

Abstract

The ability of immunomodulatory mesenchymal stromal cells (MSCs) to improve COVID-19-associated acute respiratory distress syndrome (ARDS) in clinical trials is uncertain. We assessed whether freshly cultured umbilical cord (UC)-derived MSCs improved outcomes in patients with severe COVID-19 ARDS. We enrolled 37 patients with severe COVID-19 ARDS: 15 in the phase 1 dose escalation and open label extension studies ( NCT04400032 ), and 22 patients in the phase 2b randomized clinical trial ( NCT04865107 ). Delivery of up to 270 × 106 MSCs in three divided daily doses was well tolerated and resulted in qualitative improvement in all clinical outcomes. Furthermore, MSCs resulted in resolution of lymphopenia, consistent with an important immunomodulatory effect, with significant improvement in patient reported quality-of-life measures (SF-36) at 6 months pointing to possible durable clinical effects. These findings suggest a potential benefit of freshly cultured, UC-MSCs in severe COVID-19 ARDS, associated with biological evidence of favorable immunomodulatory activity.

Details

Original languageEnglish
Article number102854
JournalStem cell reports
Volume21
Issue number4
Publication statusPublished - 14 Apr 2026
Peer-reviewedYes

External IDs

PubMed 41825447

Keywords

Keywords

  • acute respiratory distress syndrome, cell therapy, COVID-19, immunomodulation, lymphopenia, mesenchymal stem cells, randomized clinical trial, SARS-CoV2