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Genetically modified Bifidobacterium displaying Salmonella-antigen protects mice from lethal challenge of Salmonella Typhimurium in a murine typhoid fever model

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dc.contributor.authorYamamoto, Sakura-
dc.contributor.authorWada, Jun-
dc.contributor.authorKatayama, Takane-
dc.contributor.authorJikimoto, Takumi-
dc.contributor.authorNakamura, Masakuni-
dc.contributor.authorKinoshita, Shohiro-
dc.contributor.authorLee, Kyung-Mi-
dc.contributor.authorKawabata, Masato-
dc.contributor.authorShirakawa, Toshiro-
dc.date.accessioned2021-09-08T00:10:29Z-
dc.date.available2021-09-08T00:10:29Z-
dc.date.issued2010-09-24-
dc.identifier.issn0264-410X-
dc.identifier.issn1358-8745-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/115661-
dc.description.abstractWe developed a novel vaccine platform utilizing Bifidobacterium as an antigen delivery vehicle for mucosal immunization. Genetically modified Bifidobacterium longum displaying Salmonella-flagellin on the cell surface was constructed for the oral typhoid vaccine. The efficiency of this vaccine was evaluated in a murine model of typhoid fever. We then orally administered 2.5 x 10(7) CFU of the recombinant Bifidobacterium longum (vaccine) or parental Bifidobacterium longum, or PBS to BALB/C mice every other day for 2 weeks. After the administration, a total of 42 mice (14 mice in each group) were challenged with Salmonella Typhimurium (1.0 x 10(7) CFU/mouse). While 12 mice in the PBS group, and 9 in the parental Bifidobacterium longum group died (median survival: 14 and 25 days), only two in the vaccine group died. These data support that our genetically modified Bifidobacterium antigen delivery system offers a promising vaccine platform for inducing efficient mucosal immunity. (C) 2010 Elsevier Ltd. All rights reserved.-
dc.format.extent8-
dc.language영어-
dc.language.isoENG-
dc.publisherELSEVIER SCI LTD-
dc.titleGenetically modified Bifidobacterium displaying Salmonella-antigen protects mice from lethal challenge of Salmonella Typhimurium in a murine typhoid fever model-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1016/j.vaccine.2010.08.007-
dc.identifier.scopusid2-s2.0-77956494584-
dc.identifier.wosid000282734800005-
dc.identifier.bibliographicCitationVACCINE, v.28, no.41, pp 6684 - 6691-
dc.citation.titleVACCINE-
dc.citation.volume28-
dc.citation.number41-
dc.citation.startPage6684-
dc.citation.endPage6691-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaImmunology-
dc.relation.journalResearchAreaResearch & Experimental Medicine-
dc.relation.journalWebOfScienceCategoryImmunology-
dc.relation.journalWebOfScienceCategoryMedicine, Research & Experimental-
dc.subject.keywordPlusINFECTION-
dc.subject.keywordPlusDELIVERY-
dc.subject.keywordPlusVECTORS-
dc.subject.keywordPlusIMMUNOGENICITY-
dc.subject.keywordPlusIMMUNE-RESPONSES-
dc.subject.keywordPlusT-CELLS-
dc.subject.keywordPlusMUCOSAL-
dc.subject.keywordPlusVACCINE-
dc.subject.keywordPlusLIVE-
dc.subject.keywordPlusLACTOBACILLUS-
dc.subject.keywordAuthorBifidobacterium-
dc.subject.keywordAuthorMucosal vaccine-
dc.subject.keywordAuthorSalmonella-
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