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Integrin α10β1-selected mesenchymal stem cells reduced hypercoagulopathy in a porcine model of acute respiratory distress syndrome

Mesenchymal stem cells (MSCs) have been studied for their potential benefits in treating acute respiratory distress syndrome (ARDS) and have reported mild effects when trialed within human clinical trials. MSCs have been investigated in preclinical models with efficacy when administered at the time...

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Published in:Respiratory research 2023-05, Vol.24 (1), p.145-145, Article 145
Main Authors: Edström, Dag, Niroomand, Anna, Stenlo, Martin, Uvebrant, Kristina, Bölükbas, Deniz A, Hirdman, Gabriel, Broberg, Ellen, Lim, Hooi Ching, Hyllén, Snejana, Lundgren-Åkerlund, Evy, Pierre, Leif, Olm, Franziska, Lindstedt, Sandra
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creator Edström, Dag
Niroomand, Anna
Stenlo, Martin
Uvebrant, Kristina
Bölükbas, Deniz A
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Lim, Hooi Ching
Hyllén, Snejana
Lundgren-Åkerlund, Evy
Pierre, Leif
Olm, Franziska
Lindstedt, Sandra
description Mesenchymal stem cells (MSCs) have been studied for their potential benefits in treating acute respiratory distress syndrome (ARDS) and have reported mild effects when trialed within human clinical trials. MSCs have been investigated in preclinical models with efficacy when administered at the time of lung injury. Human integrin α10β1-selected adipose tissue-derived MSCs (integrin α10β1-MSCs) have shown immunomodulatory and regenerative effects in various disease models. We hypothesized that integrin α10β1 selected-MSCs can be used to treat a sepsis-induced ARDS in a porcine model when administering cells after established injury rather than simultaneously. This was hypothesized to reflect a clinical picture of treatment with MSCs in human ARDS. 12 pigs were randomized to the treated or placebo-controlled group prior to the induction of mild to moderate ARDS via lipopolysaccharide administration. The treated group received 5 × 10  cells/kg integrin α10β1-selected MSCs and both groups were followed for 12 h. ARDS was confirmed with blood gases and retrospectively with histological changes. After intervention, the treated group showed decreased need for inotropic support, fewer signs of histopathological lung injury including less alveolar wall thickening and reduction of the hypercoagulative disease state. The MSC treatment was not associated with adverse events over the monitoring period. This provides new opportunities to investigate integrin α10β1-selected MSCs as a treatment for a disease which does not yet have any definitive therapeutic options.
doi_str_mv 10.1186/s12931-023-02459-6
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subjects Acute respiratory distress syndrome
Adipose tissue
Advanced therapeutic medicinal products
Alveoli
Animal models
Animals
Basic Medicine
Body fat
Catheters
Cell and Molecular Biology
Cell- och molekylärbiologi
Clinical Medicine
Clinical trials
Cryopreservation
E coli
Good Manufacturing Practice
Health services
Immunomodulation
Injury prevention
Integrin α10β1 mesenchymal stem cells
Integrins
Klinisk medicin
Lipopolysaccharides
Lung disease
Lung Injury
Lungmedicin och allergi
Lungs
Medical and Health Sciences
Medicin och hälsovetenskap
Medicinska och farmaceutiska grundvetenskaper
Mesenchymal Stem Cell Transplantation
Mesenchymal Stem Cells
Mortality
Ostomy
Permeability
Pulmonary arteries
Respiratory distress syndrome
Respiratory Distress Syndrome - diagnosis
Respiratory Medicine and Allergy
Retrospective Studies
Sepsis
Stem cells
Swine
Ventilators
title Integrin α10β1-selected mesenchymal stem cells reduced hypercoagulopathy in a porcine model of acute respiratory distress syndrome
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