Effects of nebulized adipose-derived mesenchymal stem cells on acute lung injury following smoke inhalation in sheep

•This manuscript describes efficacy of nebulized mesenchymal stem cell on smoke inhalation-induced acute lung injury.•The one-time nebulization of 10 million mesenchymal stem cell may be insufficient to alleviate the severity of ARDS.•Further studies are needed to improve the survival of mesenchymal...

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Veröffentlicht in:International immunopharmacology 2023-10, Vol.123, p.110638-110638, Article 110638
Hauptverfasser: Niimi, Yosuke, Baljinnyam, Tuvshintugs, Fukuda, Satoshi, Andersen, Clark R., Salsbury, John R., Lee, Jong O., Prough, Donald S., Enkhbaatar, Perenlei
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Sprache:eng
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Zusammenfassung:•This manuscript describes efficacy of nebulized mesenchymal stem cell on smoke inhalation-induced acute lung injury.•The one-time nebulization of 10 million mesenchymal stem cell may be insufficient to alleviate the severity of ARDS.•Further studies are needed to improve the survival of mesenchymal stem cell in harsh airway conditions. Treatment of ARDS caused by smoke inhalation is challenging with no specific therapies available. The aim of this study was to test the efficacy of nebulized adipose-derived mesenchymal stem cells (ASCs) in a well-characterized, clinically relevant ovine model of smoke inhalation injury. Fourteen female Merino sheep were surgically instrumented 5–7 days prior to study. After induction of acute lung injury (ALI) by cooled cotton smoke insufflation into the lungs (under anesthesia and analgesia), sheep were placed on a mechanical ventilator for 48 hrs and monitored for cardiopulmonary hemodynamics in a conscious state. ASCs were isolated from ovine adipose tissue. Sheep were randomly allocated to two groups after smoke injury: 1) ASCs group (n = 6): 10 million ASCs were nebulized into the airway at 1 hr post-injury; and 2) Control group (n = 8): Nebulized with saline into the airways at 1 hr post-injury. ASCs were labeled with green fluorescent protein (GFP) to trace cells within the lung. ASCs viability was determined in bronchoalveolar lavage fluid (BALF). PaO2/FiO2 in the ASCs group was significantly higher than in the control group (p = 0.001) at 24 hrs. Oxygenation index: (mean airway pressure × FiO2/PaO2) was significantly lower in the ASCs group at 36 hr (p = 0.003). Pulmonary shunt fraction tended to be lower in the ASCs group as compared to the control group. GFP-labelled ASCs were found on the surface of trachea epithelium 48 hrs after injury. The viability of ASCs in BALF was significantly lower than those exposed to the control vehicle solution. Nebulized ASCs moderately improved pulmonary function and delayed the onset of ARDS.
ISSN:1567-5769
1878-1705
DOI:10.1016/j.intimp.2023.110638