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The Mycobacterium avium subsp paratuberculosis fibronectin attachment protein, a toll-like receptor 4 agonist, enhances dendritic cell-based cancer vaccine potency

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dc.contributor.authorNoh, Kyung Tae-
dc.contributor.authorShin, Sung Jae-
dc.contributor.authorSon, Kwang Hee-
dc.contributor.authorJung, In Duk-
dc.contributor.authorKang, Hyun Kyu-
dc.contributor.authorLee, Su Jung-
dc.contributor.authorLee, Eun Kyung-
dc.contributor.authorShin, Yong Kyoo-
dc.contributor.authorYou, Ji Chang-
dc.contributor.authorPark, Yeong-Min-
dc.date.available2019-05-29T07:34:28Z-
dc.date.issued2012-05-
dc.identifier.issn1226-3613-
dc.identifier.issn2092-6413-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/20311-
dc.description.abstractIn this study, we showed the direct interaction between Mycobacterium avium subsp. paratuberculosis fibronectin attachment protein (FAP) and toll-like receptor4 (TLR4) via co-localization and binding by using confocal microscopy and co-immunoprecipitation assays. FAP triggered the expression of pro- and anti-inflammatory cytokines in a TLR4-dependent manner. In addition, FAP-induced cytokine expression in bone marrow-derived dendritic cells (BMDCs) was modulated in part by glycogen synthase kinase-3 (GSK-3). FAP-induced expression of CD80, CD86, major histocompatibility complex (MHC) class I, and MHC class II in TLR4(+/+) BMDCs was not observed in TLR4(-/-) BMDCs. Furthermore, FAP induced DC-mediated CD8(+) T cell proliferation and cytotoxic T lymphocyte (CTL) activity, and suppressed tumor growth with DC-based tumor vaccination in EG7 thymoma murine model. Taken together, these results indicate that the TLR4 agonist, FAP, a potential immunoadjuvant for DC-based cancer vaccination, improves the DC-based immune response via the TLR4 signaling pathway.-
dc.format.extent10-
dc.language영어-
dc.language.isoENG-
dc.publisherKOREAN SOC MED BIOCHEMISTRY MOLECULAR BIOLOGY-
dc.titleThe Mycobacterium avium subsp paratuberculosis fibronectin attachment protein, a toll-like receptor 4 agonist, enhances dendritic cell-based cancer vaccine potency-
dc.typeArticle-
dc.identifier.doi10.3858/emm.2012.44.5.038-
dc.identifier.bibliographicCitationEXPERIMENTAL AND MOLECULAR MEDICINE, v.44, no.5, pp 340 - 349-
dc.identifier.kciidART001661854-
dc.description.isOpenAccessY-
dc.identifier.wosid000304896600004-
dc.identifier.scopusid2-s2.0-84861642579-
dc.citation.endPage349-
dc.citation.number5-
dc.citation.startPage340-
dc.citation.titleEXPERIMENTAL AND MOLECULAR MEDICINE-
dc.citation.volume44-
dc.type.docTypeArticle-
dc.publisher.location대한민국-
dc.subject.keywordAuthordendritic cells-
dc.subject.keywordAuthorFAP-A protein-
dc.subject.keywordAuthorMycobacterium avium-
dc.subject.keywordAuthorglycogen synthase kinase-3-
dc.subject.keywordAuthortoll-like receptor 4-
dc.subject.keywordPlusGLYCOGEN-SYNTHASE KINASE-3-
dc.subject.keywordPlusBACILLUS-CALMETTE-GUERIN-
dc.subject.keywordPlusMATURATION-
dc.subject.keywordPlusPOLARIZATION-
dc.subject.keywordPlusPURIFICATION-
dc.subject.keywordPlusMECHANISMS-
dc.subject.keywordPlusINDUCTION-
dc.subject.keywordPlusIMMUNITY-
dc.subject.keywordPlusINNATE-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaResearch & Experimental Medicine-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryMedicine, Research & Experimental-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
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