The protective effect of Tilia amurensis honey on influenza A virus infection through stimulation of interferon-mediated IFITM3 signaling
Recently, attention has focused on the prevention and treatment of respiratory viruses including influenza viruses. We evaluated the antiviral effect of Tilia amurensis honey (TH) against influenza A virus in murine macrophages. Influenza A virus infection was reduced following pretreatment with TH....
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Published in | Biomedicine & pharmacotherapy Vol. 153; p. 113259 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier Masson SAS
01.09.2022
Elsevier |
Subjects | |
Online Access | Get full text |
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Summary: | Recently, attention has focused on the prevention and treatment of respiratory viruses including influenza viruses. We evaluated the antiviral effect of Tilia amurensis honey (TH) against influenza A virus in murine macrophages. Influenza A virus infection was reduced following pretreatment with TH. Pretreatment of murine macrophages with TH increased the production and secretion of type-1 interferon (IFN) and proinflammatory cytokines and increased phosphorylation of the type-1 IFN-related proteins, TANK-binding kinase (TBK), and STAT. Moreover, TH increased the expression of IFN-stimulating genes and increased the expression of IFN-inducible transmembrane (IFITM3), a protein that interferes with virus replication and entry. Taken together, these findings suggest that TH suppresses influenza A virus infection by regulating the innate immune response in macrophages. This supports the development of preventive and therapeutic agents for influenza A virus and enhances the economic value of TH.
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•TH inhibit infection of influenza A virus in murine macrophages.•TH activates the type-1 interferon related pathway including TBK-STAT signaling.•TH increases expression of IFN-stimulating genes (ISG’s) and IFN-inducible transmembrane 3 (IFITM3)•TH could be a potential preventive and therapeutic agents for influenza A virus by modulating the regulates innate immune response. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0753-3322 1950-6007 |
DOI: | 10.1016/j.biopha.2022.113259 |