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Aging-Associated Extracellular Vesicles Contain Immune Regulatory microRNAs Alleviating Hyperinflammatory State and Immune Dysfunction in the Elderly

机译:衰老相关的细胞外囊泡含有免疫调节微大血淋减轻了老年人的高炎症状态和免疫功能障碍

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摘要

Aging-associated changes in the immune system often lead to immune dysfunction; however, the mechanisms that underlie this phenomenon have yet to be fully elucidated. This study found that the microRNA-192 (miR-192) is an aging-associated immune regulatory microRNA whose concentration was significantly increased in aged extracellular vesicles (EVs) due to the hyperinflammatory state of aged mice. Interestingly, EV miR-192 exhibited anti-inflammatory effects on macrophages. In our aged mouse model, aging was associated with prolonged inflammation in the lung upon stimulation with inactivated influenza whole virus particles (WVP), whereas EV miR-192 alleviated the prolonged inflammation associated with aging. The hyperinflammatory state of aged mice resulted in reduced production of specific antibodies and efficacy of vaccination with WVP; however, EV miR-192 attenuated this hyperinflammatory state and improved vaccination efficacy in aged mice. Our data indicate that aged EVs constitute a negative feedback loop that alleviates aging-associated immune dysfunction.
机译:免疫系统的衰老相关变化通常导致免疫功能障碍;然而,利于这种现象的机制尚未完全阐明。该研究发现,MicroRNA-192(miR-192)是一种衰老相关的免疫调节microRNA,其由于老年小鼠的炎症状态而在老年的细胞外囊泡(EV)中浓度显着增加。有趣的是,EV MIR-192对巨噬细胞表现出抗炎作用。在我们的老年小鼠模型中,在用灭活的流感整体病毒颗粒(WVP)刺激后,衰老与肺部长时间炎症有关,而EV MIR-192减轻了与老化相关的延长炎症。老年小鼠的高炎症状态导致产生特异性抗体的产生和具有WVP的疫苗接种的功效;然而,EV miR-192减毒了这种高炎症状态并改善了老年小鼠的疫苗接种效果。我们的数据表明,年龄的EVS构成了一种负反馈环,可减轻衰老相关的免疫功能障碍。

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