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Anti-Viral Activities of Umbilical Cord Mesenchymal Stem Cell-Derived Small Extracellular Vesicles Against Human Respiratory Viruses.
Oh, Soo-Jin; Lee, Eun-Na; Park, Joo-Hoo; Lee, Jae Kyung; Cho, Geum Joon; Park, Il-Ho; Shin, Ok Sarah.
  • Oh SJ; BK21 Graduate program, Department of Biomedical Sciences, College of Medicine, Korea University Guro Hospital, Seoul, South Korea.
  • Lee EN; Department of Medicine, Korea University College of Medicine, Seoul, South Korea.
  • Park JH; Department of Otorhinolaryngology-Head and Neck Surgery, Korea University College of Medicine, Seoul, South Korea.
  • Lee JK; Upper Airway Chronic Inflammatory Diseases Laboratory, Korea University, Seoul, South Korea.
  • Cho GJ; BK21 Graduate program, Department of Biomedical Sciences, College of Medicine, Korea University Guro Hospital, Seoul, South Korea.
  • Park IH; Department of Obstetrics and Gynecology, College of Medicine, Korea University Guro Hospital, Seoul, South Korea.
  • Shin OS; Department of Otorhinolaryngology-Head and Neck Surgery, Korea University College of Medicine, Seoul, South Korea.
Front Cell Infect Microbiol ; 12: 850744, 2022.
Article in English | MEDLINE | ID: covidwho-1952256
ABSTRACT
The endemic and pandemic caused by respiratory virus infection are a major cause of mortality and morbidity globally. Thus, broadly effective antiviral drugs are needed to treat respiratory viral diseases. Small extracellular vesicles derived from human umbilical cord mesenchymal stem cells (U-exo) have recently gained attention as a cell-free therapeutic strategy due to their potential for safety and efficacy. Anti-viral activities of U-exo to countermeasure respiratory virus-associated diseases are currently unknown. Here, we tested the antiviral activities of U-exo following influenza A/B virus (IFV) and human seasonal coronavirus (HCoV) infections in vitro. Cells were subject to IFV or HCoV infection followed by U-exo treatment. U-exo treatment significantly reduced IFV or HCoV replication and combined treatment with recombinant human interferon-alpha protein (IFN-α) exerted synergistically enhanced antiviral effects against IFV or HCoV. Interestingly, microRNA (miR)-125b, which is one of the most abundantly expressed small RNAs in U-exo, was found to suppress IFV replication possibly via the induction of IFN-stimulated genes (ISGs). Furthermore, U-exo markedly enhanced RNA virus-triggered IFN signaling and ISGs production. Similarly, human nasal epithelial cells cultured at the air-liquid interface (ALI) studies broadly effective anti-viral and anti-inflammatory activities of U-exo against IFV and HCoV, suggesting the potential role of U-exo as a promising intervention for respiratory virus-associated diseases.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Coronavirus / Exosomes / Mesenchymal Stem Cells / Extracellular Vesicles Limits: Humans Language: English Journal: Front Cell Infect Microbiol Year: 2022 Document Type: Article Affiliation country: Fcimb.2022.850744

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Coronavirus / Exosomes / Mesenchymal Stem Cells / Extracellular Vesicles Limits: Humans Language: English Journal: Front Cell Infect Microbiol Year: 2022 Document Type: Article Affiliation country: Fcimb.2022.850744