Back to Search Start Over

Wharton's Jelly Mesenchymal Stem Cell-Derived Extracellular Vesicles Reduce SARS-CoV2-Induced Inflammatory Cytokines Under High Glucose and Uremic Toxin Conditions.

Authors :
Khanh, Vuong Cat
Fukushige, Mizuho
Chang, Yun Hsuan
Hoang, Ngo Nhat
Yamashita, Toshiharu
Obata-Yasuoka, Mana
Hamada, Hiromi
Osaka, Motoo
Hiramatsu, Yuji
Ohneda, Osamu
Source :
Stem Cells & Development. 8/1/2021, Vol. 30 Issue 15, p758-772. 15p.
Publication Year :
2021

Abstract

Cytokine storm is recognized as one of the factors contributing to organ failures and mortality in patients with COVID-19. Due to chronic inflammation, COVID-19 patients with diabetes mellitus (DM) or renal disease (RD) have more severe symptoms and higher mortality. However, the factors that contribute to severe outcomes of COVID-19 patients with DM and RD have received little attention. In an effort to investigate potential treatments for COVID-19, recent research has focused on the immunomodulation functions of mesenchymal stem cells (MSCs). In this study, the correlation between DM and RD and the severity of COVID-19 was examined by a combined approach with a meta-analysis and experimental research. The results of a systematic review and meta-analysis suggested that the odd of mortality in patients with both DM and RD was increased in comparison to those with a single comorbidity. In addition, in the experimental research, the data showed that high glucose and uremic toxins contributed to the induction of cytokine storm in human lung adenocarcinoma epithelial cells (Calu-3 cells) in response to SARS-CoV Peptide Pools. Of note, the incorporation of Wharton's jelly MSC-derived extracellular vesicles (WJ-EVs) into SARS-CoV peptide-induced Calu-3 resulted in a significant decrease in nuclear NF-κB p65 and the downregulation of the cytokine storm under high concentrations of glucose and uremic toxins. This clearly suggests the potential for WJ-EVs to reduce cytokine storm reactions in patients with both chronic inflammation diseases and viral infection. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
15473287
Volume :
30
Issue :
15
Database :
Academic Search Index
Journal :
Stem Cells & Development
Publication Type :
Academic Journal
Accession number :
151723020
Full Text :
https://doi.org/10.1089/scd.2021.0065