Mesenchymal Stem Cell Therapy for Severe COVID-19 ARDS.


Journal

Journal of intensive care medicine
ISSN: 1525-1489
Titre abrégé: J Intensive Care Med
Pays: United States
ID NLM: 8610344

Informations de publication

Date de publication:
Jun 2021
Historique:
pubmed: 6 3 2021
medline: 29 5 2021
entrez: 5 3 2021
Statut: ppublish

Résumé

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. 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. MSC infusion is a safe treatment for COVID-19 ARDS that improves pulmonary function and overall outcome in this patient population.

Sections du résumé

BACKGROUND 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 RESULTS
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 CONCLUSIONS
MSC infusion is a safe treatment for COVID-19 ARDS that improves pulmonary function and overall outcome in this patient population.

Identifiants

pubmed: 33663244
doi: 10.1177/0885066621997365
pmc: PMC8145440
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

681-688

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Auteurs

Helene Häberle (H)

Department of Anaesthesiology and Intensive Care Medicine, University Hospital Tübingen, 9188Eberhard-Karls-University, Tübingen, Germany.

Harry Magunia (H)

Department of Anaesthesiology and Intensive Care Medicine, University Hospital Tübingen, 9188Eberhard-Karls-University, Tübingen, Germany.

Peter Lang (P)

Department I-General Pediatrics, Hematology/Oncology, University Children's Hospital Tübingen, Tübingen, Germany.

Henning Gloeckner (H)

Department of Anaesthesiology and Intensive Care Medicine, University Hospital Tübingen, 9188Eberhard-Karls-University, Tübingen, Germany.

Andreas Körner (A)

Department of Anaesthesiology and Intensive Care Medicine, University Hospital Tübingen, 9188Eberhard-Karls-University, Tübingen, Germany.

Michael Koeppen (M)

Department of Anaesthesiology and Intensive Care Medicine, University Hospital Tübingen, 9188Eberhard-Karls-University, Tübingen, Germany.

Tamam Backchoul (T)

Center for Clinical Transfusion Medicine, University of Tübingen, Tübingen, Germany.
Transfusion Medicine, Medical Faculty of Tübingen, Tübingen, Germany.

Nisar Malek (N)

Innere Medizin I, Universitätsklinikum Tübingen, Tübingen, Germany.

Rupert Handgretinger (R)

Department I-General Pediatrics, Hematology/Oncology, University Children's Hospital Tübingen, Tübingen, Germany.

Peter Rosenberger (P)

Department of Anaesthesiology and Intensive Care Medicine, University Hospital Tübingen, 9188Eberhard-Karls-University, Tübingen, Germany.

Valbona Mirakaj (V)

Department of Anaesthesiology and Intensive Care Medicine, University Hospital Tübingen, 9188Eberhard-Karls-University, Tübingen, Germany.

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