Role of specialized pro-resolving lipid mediators and their receptors in virus infection: a promising therapeutic strategy for SARS-CoV-2 cytokine stormopen access
- Authors
- Lee, Chang Hoon
- Issue Date
- Jan-2021
- Publisher
- PHARMACEUTICAL SOC KOREA
- Keywords
- Virus infection; Specialized pro-resolving lipid mediators; Chemerin receptor 1; FPR2/ALX, SARS-CoV2; Cytokine storm
- Citation
- ARCHIVES OF PHARMACAL RESEARCH, v.44, no.1, pp 84 - 98
- Pages
- 15
- Indexed
- SCIE
SCOPUS
KCI
- Journal Title
- ARCHIVES OF PHARMACAL RESEARCH
- Volume
- 44
- Number
- 1
- Start Page
- 84
- End Page
- 98
- URI
- https://scholarworks.dongguk.edu/handle/sw.dongguk/5530
- DOI
- 10.1007/s12272-020-01299-y
- ISSN
- 0253-6269
1976-3786
- Abstract
- 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.
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Collections - College of Pharmacy > Department of Pharmacy > 1. Journal Articles

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