» Articles » PMID: 35321737

Mesenchymal Stem/stromal Cell Therapy for COVID-19 Pneumonia: Potential Mechanisms, Current Clinical Evidence, and Future Perspectives

Overview
Publisher Biomed Central
Date 2022 Mar 24
PMID 35321737
Authors
Affiliations
Soon will be listed here.
Abstract

The coronavirus disease 2019 (COVID-19) pandemic, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has spread into more than 200 countries and infected approximately 203 million people globally. COVID-19 is associated with high mortality and morbidity in some patients, and this disease still does not have effective treatments with reproducibly appreciable outcomes. One of the leading complications associated with COVID-19 is acute respiratory distress syndrome (ARDS); this is an anti-viral host inflammatory response, and it is usually caused by a cytokine storm syndrome which may lead to multi-organ failure and death. Currently, COVID-19 patients are treated with approaches that mostly fall into two major categories: immunomodulators, which promote the body's fight against viruses efficiently, and antivirals, which slow or stop viruses from multiplying. These treatments include a variety of novel therapies that are currently being tested in clinical trials, including serum, IL-6 antibody, and remdesivir; however, the outcomes of these therapies are not consistently appreciable and remain a subject of debate. Mesenchymal stem/stromal cells (MSCs), the multipotent stem cells that have previously been used to treat viral infections and various respiratory diseases such as ARDS exhibit immunomodulatory properties and can ameliorate tissue damage. Given that SARS-CoV-2 targets the immune system and causes tissue damage, it is presumable that MSCs are being explored to treat COVID-19 patients. This review summarizes the potential mechanisms of action of MSC therapy, progress of MSC, and its related products in clinical trials for COVID-19 therapy based on the outcomes of these clinical studies.

Citing Articles

Persistent tailoring of MSC activation through genetic priming.

Beauregard M, Bedford G, Brenner D, Sanchez Solis L, Nishiguchi T, Abhimanyu Mol Ther Methods Clin Dev. 2024; 32(3):101316.

PMID: 39282077 PMC: 11396059. DOI: 10.1016/j.omtm.2024.101316.


Mesenchymal stromal cells (MSCs) as a therapeutic agent of inflammatory disease and infectious COVID-19 virus: live or dead mesenchymal?.

Kheder R, Darweesh O, Hussen B, Abdullah S, Basiri A, Taheri M Mol Biol Rep. 2024; 51(1):295.

PMID: 38340168 DOI: 10.1007/s11033-023-09174-x.


Effectiveness and safety of normoxic allogenic umbilical cord mesenchymal stem cells administered as adjunctive treatment in patients with severe COVID-19.

Soetjahjo B, Malueka R, Nurudhin A, Purwoko , Sumardi , Wisaksana R Sci Rep. 2023; 13(1):12520.

PMID: 37532730 PMC: 10397314. DOI: 10.1038/s41598-023-39268-2.


Exploring the Immunomodulatory Properties of Stem Cells in Combating COVID-19: Can We Expect More?.

Mallis P Bioengineering (Basel). 2023; 10(7).

PMID: 37508830 PMC: 10376782. DOI: 10.3390/bioengineering10070803.


A shared genetic contribution to osteoarthritis and COVID-19 outcomes: a large-scale genome-wide cross-trait analysis.

Huang Y, Tian T, Huang J, Wang J, Sui C, Ni J Front Immunol. 2023; 14:1184958.

PMID: 37398645 PMC: 10311546. DOI: 10.3389/fimmu.2023.1184958.


References
1.
Dilogo I, Aditianingsih D, Sugiarto A, Burhan E, Damayanti T, Sitompul P . Umbilical cord mesenchymal stromal cells as critical COVID-19 adjuvant therapy: A randomized controlled trial. Stem Cells Transl Med. 2021; 10(9):1279-1287. PMC: 8242692. DOI: 10.1002/sctm.21-0046. View

2.
Newman R, Yoo D, Leroux M, Danilkovitch-Miagkova A . Treatment of inflammatory diseases with mesenchymal stem cells. Inflamm Allergy Drug Targets. 2009; 8(2):110-23. DOI: 10.2174/187152809788462635. View

3.
Guery B, Mason C, Dobard E, Beaucaire G, Summer W, Nelson S . Keratinocyte growth factor increases transalveolar sodium reabsorption in normal and injured rat lungs. Am J Respir Crit Care Med. 1997; 155(5):1777-84. DOI: 10.1164/ajrccm.155.5.9154891. View

4.
Huang I, Bailey C, Weyer J, Radoshitzky S, Becker M, Chiang J . Distinct patterns of IFITM-mediated restriction of filoviruses, SARS coronavirus, and influenza A virus. PLoS Pathog. 2011; 7(1):e1001258. PMC: 3017121. DOI: 10.1371/journal.ppat.1001258. View

5.
Gattinoni L, Coppola S, Cressoni M, Busana M, Rossi S, Chiumello D . COVID-19 Does Not Lead to a "Typical" Acute Respiratory Distress Syndrome. Am J Respir Crit Care Med. 2020; 201(10):1299-1300. PMC: 7233352. DOI: 10.1164/rccm.202003-0817LE. View