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A Ceramide Analogue Stimulates Dendritic Cells To Promote T Cell Responses upon Virus Infections

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dc.contributor.authorPritzl, Curtis J.-
dc.contributor.authorSeo, Young-Jin-
dc.contributor.authorXia, Chuan-
dc.contributor.authorVijayan, Madhuvanthi-
dc.contributor.authorStokes, Zachary D.-
dc.contributor.authorHahm, Bumsuk-
dc.date.accessioned2022-05-09T09:40:05Z-
dc.date.available2022-05-09T09:40:05Z-
dc.date.issued2015-05-
dc.identifier.issn0022-1767-
dc.identifier.issn1550-6606-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/57454-
dc.description.abstractThe ceramide family of lipids plays important roles in both cell structure and signaling in a diverse array of cell types, including immune cells. However, very little is known regarding how ceramide affects the activation of dendritic cells (DCs) in response to viral infection. In this study, we demonstrate that a synthetic ceramide analog (C8) stimulates DCs to increase the expansion of virus-specific T cells upon virus infection. Exogenously supplied C8 ceramide elevated the expression of DC maturation markers such as MHC class I and costimulatory molecules following infection with the clone 13 strain of lymphocytic choriomeningitis virus (LCMV) or influenza virus. Importantly, ceramide-conditioned, LCMV-infected DCs displayed an increased ability to promote expansion of virus-specific CD8(+) T cells when compared with virus-infected DCs. Furthermore, a locally instilled ceramide analog significantly increased virus-reactive T cell responses in vivo to both LCMV and influenza virus infections. Collectively, these findings provide new insights into ceramide-mediated regulation of DC responses against virus infection and help us establish a foundation for novel immune-stimulatory therapeutics.-
dc.format.extent11-
dc.language영어-
dc.language.isoENG-
dc.publisherAMER ASSOC IMMUNOLOGISTS-
dc.titleA Ceramide Analogue Stimulates Dendritic Cells To Promote T Cell Responses upon Virus Infections-
dc.typeArticle-
dc.identifier.doi10.4049/jimmunol.1402672-
dc.identifier.bibliographicCitationJOURNAL OF IMMUNOLOGY, v.194, no.9, pp 4339 - 4349-
dc.description.isOpenAccessY-
dc.identifier.wosid000353727400032-
dc.identifier.scopusid2-s2.0-84928485431-
dc.citation.endPage4349-
dc.citation.number9-
dc.citation.startPage4339-
dc.citation.titleJOURNAL OF IMMUNOLOGY-
dc.citation.volume194-
dc.type.docTypeArticle-
dc.publisher.location미국-
dc.subject.keywordPlusCHRONIC VIRAL-INFECTION-
dc.subject.keywordPlusPERSISTENT LCMV INFECTION-
dc.subject.keywordPlusIMMUNE-RESPONSES-
dc.subject.keywordPlusOXIDATIVE STRESS-
dc.subject.keywordPlusAAL-R-
dc.subject.keywordPlusANTIGEN PRESENTATION-
dc.subject.keywordPlusADAPTIVE IMMUNITY-
dc.subject.keywordPlusINDUCED APOPTOSIS-
dc.subject.keywordPlusRECEPTOR DEC-205-
dc.subject.keywordPlusUP-REGULATION-
dc.relation.journalResearchAreaImmunology-
dc.relation.journalWebOfScienceCategoryImmunology-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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