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肥胖驱动的特异性促解决介质缺陷可能导致 SARS-CoV-2 感染期间的不良后果。

Obesity-Driven Deficiencies of Specialized Pro-resolving Mediators May Drive Adverse Outcomes During SARS-CoV-2 Infection.

机构信息

Department of Nutrition, Gillings School of Global Public Health and School of Medicine, The University of North Carolina at Chapel Hill, Chapel Hill, NC, United States.

Division of Pulmonary, Critical Care and Sleep Medicine, The Ohio State University Wexner Medical Center, Davis Heart and Lung Research Institute, Columbus, OH, United States.

出版信息

Front Immunol. 2020 Aug 11;11:1997. doi: 10.3389/fimmu.2020.01997. eCollection 2020.

DOI:10.3389/fimmu.2020.01997
PMID:32983141
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7438933/
Abstract

Obesity is a major independent risk factor for increased morbidity and mortality upon infection with Severe Acute Respiratory Syndrome Coronavirus (SARS-CoV-2), which is responsible for the current coronavirus disease pandemic (COVID-19). Therefore, there is a critical need to identify underlying metabolic factors associated with obesity that could be contributing toward increased susceptibility to SARS-CoV-2 in this vulnerable population. Here, we focus on the critical role of potent endogenous lipid metabolites known as specialized pro-resolving mediators (SPMs) that are synthesized from polyunsaturated fatty acids. SPMs are generated during the transition of inflammation to resolution and have a vital role in directing damaged tissues to homeostasis; furthermore, SPMs display anti-viral activity in the context of influenza infection without being immunosuppressive. We cover evidence from rodent and human studies to show that obesity, and its co-morbidities, induce a signature of SPM deficiency across immunometabolic tissues. We further discuss how the effects of obesity upon SARS-CoV-2 infection are likely exacerbated with environmental exposures that promote chronic pulmonary inflammation and augment SPM deficits. Finally, we highlight potential approaches to overcome the loss of SPMs using dietary and pharmacological interventions. Collectively, this mini-review underscores the need for mechanistic studies on how SPM deficiencies driven by obesity and environmental exposures may exacerbate the response to SARS-CoV-2.

摘要

肥胖是严重急性呼吸综合征冠状病毒(SARS-CoV-2)感染后发病率和死亡率增加的一个主要独立危险因素,SARS-CoV-2 引发了当前的冠状病毒病大流行(COVID-19)。因此,迫切需要确定与肥胖相关的潜在代谢因素,这些因素可能导致肥胖人群对 SARS-CoV-2 的易感性增加。在这里,我们重点关注强效内源性脂质代谢物(称为特异性促解决介质,SPM)的关键作用,这些脂质代谢物是由多不饱和脂肪酸合成的。SPM 是在炎症向解决的转变过程中产生的,在引导受损组织恢复到平衡状态方面发挥着重要作用;此外,SPM 在流感感染的情况下具有抗病毒活性,而不会产生免疫抑制作用。我们综述了来自啮齿动物和人类研究的证据,表明肥胖及其合并症会导致免疫代谢组织中 SPM 缺乏的特征。我们进一步讨论了肥胖对 SARS-CoV-2 感染的影响如何因促进慢性肺部炎症和加剧 SPM 缺乏的环境暴露而加剧。最后,我们强调了使用饮食和药物干预来克服 SPM 损失的潜在方法。总的来说,这篇迷你综述强调了需要进行机制研究,以了解肥胖和环境暴露引起的 SPM 缺乏如何加剧对 SARS-CoV-2 的反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4d4/7438933/d42740d4d512/fimmu-11-01997-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4d4/7438933/d42740d4d512/fimmu-11-01997-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4d4/7438933/d42740d4d512/fimmu-11-01997-g0001.jpg

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