Anti-Viral Activities of Umbilical Cord Mesenchymal Stem Cell-Derived Small Extracellular Vesicles Against Human Respiratory Viruses

被引:14
|
作者
Oh, Soo-Jin [1 ]
Lee, Eun-Na [2 ]
Park, Joo-Hoo [3 ,4 ]
Lee, Jae Kyung [1 ]
Cho, Geum Joon [5 ]
Park, Il-Ho [3 ,4 ]
Shin, Ok Sarah [1 ,2 ]
机构
[1] Korea Univ, Coll Med, Dept Biomed Sci, Grad program BK21,Guro Hosp, Seoul, South Korea
[2] Korea Univ, Dept Med, Coll Med, Seoul, South Korea
[3] Korea Univ, Dept Otorhinolaryngol Head & Neck Surg, Coll Med, Seoul, South Korea
[4] Korea Univ, Upper Airway Chron Inflammatory Dis Lab, Seoul, South Korea
[5] Korea Univ, Coll Med, Dept Obstet & Gynecol, Guro Hosp, Seoul, South Korea
基金
新加坡国家研究基金会;
关键词
small extracellular vesicles (exosomes); UCMSCs; respiratory viruses; anti-viral; ALI (Air-Liquid Interface); EXOSOME; MICRORNAS; INHIBIT;
D O I
10.3389/fcimb.2022.850744
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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-alpha) 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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页数:14
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