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SARS-CoV-2-mediated evasion strategies for antiviral interferon pathways

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dc.contributor.authorOh, Soo-Jin-
dc.contributor.authorShin, Ok Sarah-
dc.date.accessioned2022-04-18T08:42:49Z-
dc.date.available2022-04-18T08:42:49Z-
dc.date.created2022-04-18-
dc.date.issued2022-03-
dc.identifier.issn1225-8873-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/140279-
dc.description.abstractWith global expansion of the COVID-19 pandemic and the emergence of new variants, extensive efforts have been made to develop highly effective antiviral drugs and vaccines against SARS-CoV-2. The interactions of coronaviruses with host antiviral interferon pathways ultimately determine successful viral replication and SARS-CoV-2-induced pathogenesis. Innate immune receptors play an essential role in host defense against SARS-CoV-2 via the induction of IFN production and signaling. Here, we summarize the recent advances in innate immune sensing mechanisms of SARS-CoV-2 and various strategies by which SARS-CoV-2 antagonizes antiviral innate immune signaling pathways, with a particular focus on mechanisms utilized by multiple SARS-CoV-2 proteins to evade interferon induction and signaling in host cell. Understanding the underlying immune evasion mechanisms of SARS-CoV-2 is essential for the improvement of vaccines and therapeutic strategies.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherMICROBIOLOGICAL SOCIETY KOREA-
dc.subjectNUCLEAR IMPORT-
dc.subjectPROTEASE-
dc.subjectNUP98-
dc.titleSARS-CoV-2-mediated evasion strategies for antiviral interferon pathways-
dc.typeArticle-
dc.contributor.affiliatedAuthorShin, Ok Sarah-
dc.identifier.doi10.1007/s12275-022-1525-1-
dc.identifier.scopusid2-s2.0-85124254948-
dc.identifier.wosid000751590600001-
dc.identifier.bibliographicCitationJOURNAL OF MICROBIOLOGY, v.60, no.3, pp.290 - 299-
dc.relation.isPartOfJOURNAL OF MICROBIOLOGY-
dc.citation.titleJOURNAL OF MICROBIOLOGY-
dc.citation.volume60-
dc.citation.number3-
dc.citation.startPage290-
dc.citation.endPage299-
dc.type.rimsART-
dc.type.docTypeReview-
dc.identifier.kciidART002813848-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaMicrobiology-
dc.relation.journalWebOfScienceCategoryMicrobiology-
dc.subject.keywordPlusNUCLEAR IMPORT-
dc.subject.keywordPlusPROTEASE-
dc.subject.keywordPlusNUP98-
dc.subject.keywordAuthorSARS-CoV-2-
dc.subject.keywordAuthorCOVID-19-
dc.subject.keywordAuthorinterferon-
dc.subject.keywordAuthorimmunity-
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