ExoCoBio Exosome Institute (EEI), ExoCoBio Inc., STE 306, 19 Gasan digital 1-ro, Geumcheon-gu, Seoul, Republic of Korea.
Krefting Research Centre, The Sahlgrenska Academy, BOX 424, Gothenburg, Sweden.
J Extracell Vesicles. 2024 Sep;13(9):e12495. doi: 10.1002/jev2.12495.
Mesenchymal stem cell (MSC)-derived extracellular vesicles (EVs) have shown anti-inflammatory potential in multiple inflammatory diseases. In the March 2022 issue of the Journal of Extracellular Vesicles, it was shown that EVs from human MSCs can suppress severe acute respiratory distress syndrome, coronavirus 2 (SARS-CoV-2) replication and can mitigate the production and release of infectious virions. We therefore hypothesized that MSC-EVs have an anti-viral effect in SARS-CoV-2 infection in vivo. We extended this question to ask whether also other respiratory viral infections could be treated by MSC-EVs. Adipose stem cell-derived EVs (ASC-EVs) were isolated using tangential flow filtration from conditioned media obtained from a multi-flask cell culture system. The effects of the ASC-EVs were tested in Vero E6 cells in vitro. ASC-EVs were also given i.v. to SARS-CoV-2 infected Syrian Hamsters, and H1N1 influenza virus infected mice. The ASC-EVs attenuated SARS-CoV-2 virus replication in Vero E6 cells and reduced body weight and signs of lung injury in infected Syrian hamsters. Furthermore, ASC-EVs increased the survival rate of influenza A-infected mice and attenuated signs of lung injury. In summary, this study suggests that ASC-EVs can have beneficial therapeutic effects in models of virus-infection-associated acute lung injury and may potentially be developed to treat lung injury in humans.
间充质干细胞(MSC)衍生的细胞外囊泡(EVs)在多种炎症性疾病中显示出抗炎潜力。在 2022 年 3 月的《细胞外囊泡杂志》上,研究表明来自人 MSC 的 EVs 可以抑制严重急性呼吸窘迫综合征、冠状病毒 2(SARS-CoV-2)复制,并可以减轻传染性病毒粒子的产生和释放。因此,我们假设 MSC-EVs 在 SARS-CoV-2 感染的体内具有抗病毒作用。我们扩展了这个问题,询问 MSC-EVs 是否也可以治疗其他呼吸道病毒感染。脂肪干细胞衍生的 EVs(ASC-EVs)通过从多瓶细胞培养系统获得的条件培养基中使用切向流过滤分离得到。在体外的 Vero E6 细胞中测试了 ASC-EVs 的作用。还将 ASC-EVs 静脉内给予 SARS-CoV-2 感染的叙利亚仓鼠和感染 H1N1 流感病毒的小鼠。ASC-EVs 减弱了 Vero E6 细胞中的 SARS-CoV-2 病毒复制,并减轻了感染的叙利亚仓鼠的体重和肺部损伤迹象。此外,ASC-EVs 增加了感染流感 A 的小鼠的存活率,并减轻了肺部损伤的迹象。总之,这项研究表明,ASC-EVs 可以在与病毒感染相关的急性肺损伤模型中具有有益的治疗效果,并且可能被开发用于治疗人类的肺部损伤。