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Efficient induction of T helper type 1-mediated immune responses in antigen-primed mice by anti-CD3 single-chain Fv/interleukin-18 fusion DNA

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dc.contributor.authorKim, EJ-
dc.contributor.authorCho, D-
dc.contributor.authorKim, TS-
dc.date.available2021-02-22T16:03:16Z-
dc.date.issued2004-01-
dc.identifier.issn0019-2805-
dc.identifier.issn1365-2567-
dc.identifier.urihttps://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/15909-
dc.description.abstractTwo types of T helper (Th) cells - Th1 and Th2 - play different roles in protection and immunopathology. The Th1 cell-mediated immune response plays an important role in inducing the host defence against intracellular bacteria and also in cancer immunotherapy. To effectively induce Th1 immune responses, we constructed a mammalian expression plasmid (pAnti-CD3sFv/IL-18) carrying a fusion gene in which anti-CD3 single-chain Fv (sFv) cDNA, the smallest unit of antibody recognizing the CD3 epsilon moiety of the T-cell receptor, was covalently linked to mature interleukin (IL)-18 cDNA. Intramuscular injection of ovalbumin (OVA)-sensitized BALB/c mice with pAnti-CD3sFv/IL-18 DNA efficiently increased the production of both OVA-specific interferon-gamma and anti-OVA immunoglobulin G2a, compared to injection with pAnti-CD3sFv DNA. In addition, pAnti-CD3sFv/IL-18 was more efficient than a mixture of pAnti-CD3sFv + pIL-18 in inducing OVA-specific, Th1 immune responses and also in inhibiting OVA-specific, IL-4 production. These studies indicate that vaccination with pAnti-CD3sFv/IL-18 fusion DNA efficiently induces the Th1 immune response in antigen-sensitized mice.-
dc.format.extent8-
dc.language영어-
dc.language.isoENG-
dc.publisherWILEY-
dc.titleEfficient induction of T helper type 1-mediated immune responses in antigen-primed mice by anti-CD3 single-chain Fv/interleukin-18 fusion DNA-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1111/j.1365-2567.2004.01784.x-
dc.identifier.scopusid2-s2.0-0347555461-
dc.identifier.wosid000187406100006-
dc.identifier.bibliographicCitationIMMUNOLOGY, v.111, no.1, pp 27 - 34-
dc.citation.titleIMMUNOLOGY-
dc.citation.volume111-
dc.citation.number1-
dc.citation.startPage27-
dc.citation.endPage34-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaImmunology-
dc.relation.journalWebOfScienceCategoryImmunology-
dc.subject.keywordPlusINTERFERON-GAMMA PRODUCTION-
dc.subject.keywordPlusDIRECT GENE-TRANSFER-
dc.subject.keywordPlusIN-VIVO-
dc.subject.keywordPlusB-CELLS-
dc.subject.keywordPlusINTERLEUKIN-18-
dc.subject.keywordPlusIL-18-
dc.subject.keywordPlusTH1-
dc.subject.keywordPlusINJECTION-
dc.subject.keywordPlusCYTOKINE-
dc.subject.keywordPlusACTIVATION-
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