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Efficacy of MSC in Patients with Severe COVID-19: Analysis of the Literature and a Case Study

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Date 2022 Oct 1
PMID 36181766
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Abstract

Patients with severe COVID-19 experience cytokine storm, an uncontrolled upregulation of pro-inflammatory cytokines, which if unresolved leads to acute respiratory distress syndrome (ARDS), organ damage, and death. Treatments with mesenchymal stromal cells (MSC) [Viswanathan S, Shi Y, Galipeau J, et al. Mesenchymal stem versus stromal cells: International Society for Cell & Gene Therapy Mesenchymal Stromal Cell committee position statement on nomenclature. Cytotherapy. 2019;21:1019-1024] appear to be effective in reducing morbidity and mortality. MSC respond to pro-inflammatory cytokines by releasing anti-inflammatory factors and mobilizing immune cells. We analyzed 82 COVID-19 clinical trials registered at ClinicalTrials.gov to determine MSC dosing, routes of administration, and outcome measures. Nearly all trials described the use of intravenous delivery with most doses ranging between 50 and 125 million MSC/treatment, which overlaps with a minimal effective dose range that we described previously. We also searched the literature to analyze clinical trial reports that used MSC to treat COVID-19. MSC were found to improve survival and oxygenation, increase discharge from intensive care units and hospitals, and reduce levels of pro-inflammatory markers. We report on a 91-year-old man with severe COVID-19 who responded rapidly to MSC treatment with transient reductions in several pro-inflammatory markers and delayed improvement in oxygenation. The results suggest that frequent monitoring of pro-inflammatory markers for severe COVID-19 will provide improved treatment guidelines by determining relationships between cytokine storms and ARDS. We propose that markers for cytokine storm are leading indicators for ARDS and that measurement of cytokines will indicate earlier treatment with MSC than is performed now for ARDS in severe COVID-19.

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References
1.
Galipeau J, Krampera M, Leblanc K, Nolta J, Phinney D, Shi Y . Mesenchymal stromal cell variables influencing clinical potency: the impact of viability, fitness, route of administration and host predisposition. Cytotherapy. 2021; 23(5):368-372. PMC: 11708105. DOI: 10.1016/j.jcyt.2020.11.007. View

2.
Hashemian S, Aliannejad R, Zarrabi M, Soleimani M, Vosough M, Hosseini S . Mesenchymal stem cells derived from perinatal tissues for treatment of critically ill COVID-19-induced ARDS patients: a case series. Stem Cell Res Ther. 2021; 12(1):91. PMC: 7844804. DOI: 10.1186/s13287-021-02165-4. View

3.
Wagner B, Henschler R . Fate of intravenously injected mesenchymal stem cells and significance for clinical application. Adv Biochem Eng Biotechnol. 2013; 130:19-37. DOI: 10.1007/10_2012_155. View

4.
Qeadan F, Tingey B, Gu L, Hafen Packard A, Erdei E, Saeed A . Prognostic Values of Serum Ferritin and D-Dimer Trajectory in Patients with COVID-19. Viruses. 2021; 13(3). PMC: 7998367. DOI: 10.3390/v13030419. View

5.
Shu L, Niu C, Li R, Huang T, Wang Y, Huang M . Treatment of severe COVID-19 with human umbilical cord mesenchymal stem cells. Stem Cell Res Ther. 2020; 11(1):361. PMC: 7432540. DOI: 10.1186/s13287-020-01875-5. View