Role of specialized pro-resolving lipid mediators and their receptors in virus infection: a promising therapeutic strategy for SARS-CoV-2 cytokine storm

被引:34
|
作者
Lee, Chang Hoon [1 ]
机构
[1] Dongguk Univ, Coll Pharm, Seoul 100715, South Korea
基金
新加坡国家研究基金会;
关键词
Virus infection; Specialized pro-resolving lipid mediators; Chemerin receptor 1; FPR2/ALX; SARS-CoV2; Cytokine storm; PROTEIN-COUPLED RECEPTOR; ALTERNATIVELY ACTIVATED MACROPHAGES; ASPIRIN-TRIGGERED LIPOXINS; PEPTIDE RECEPTOR; DOCOSAHEXAENOIC ACID; ACUTE-INFLAMMATION; CHEMERIN RECEPTOR; NEUROPROTECTIN D1; INFLUENZA-VIRUS; LEUKOTRIENE B-4;
D O I
10.1007/s12272-020-01299-y
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Unexpected viral infections outbreaks, significantly affect human health, leading to increased mortality and life disruption. Among them is the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) which emerged as a deadly pandemic, calling for intense research efforts on its pathogenicity mechanism and development of therapeutic strategies. In the SARS-CoV-2 cytokine storm, systemic inflammation has been associated with severe illness and mortality. Recent studies have demonstrated special pro-resolving lipids mediators (SPMs) lipoxins, resolvins, maresins, and protectins as potential therapeutic options for abnormal viral-triggered inflammation. Pro-resolving lipids mediators have shown great promise for the treatment of Herpes simplex virus, respiratory syncytial virus, human immunodeficiency virus, and hepatitis C virus. Based on this, studies are being conducted on their therapeutic effects in SARS-CoV-2 infection. In this review, we discussed SPMs and reviewed evidence from recent studies on SPMs as therapeutic options for viral infections, including SARS-CoV2. Based on our analysis of the previous study, we argue that SPMs are a potential treatment for SARS-CoV-2 infection and other viral infections. We expect further research on how SPMs modulate viral-triggered inflammation through G-protein-coupled receptors (GPCRs), and chemical stability and druggability of SPMs.
引用
收藏
页码:84 / 98
页数:15
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