The flavonoid ellagic acid from a medicinal herb inhibits host immune tolerance induced by the hepatitis B virus-e antigen

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dc.contributor.authorE H Kang-
dc.contributor.authorT Y Kown-
dc.contributor.authorG T Oh-
dc.contributor.authorW F Park-
dc.contributor.authorS I Park-
dc.contributor.authorS K Park-
dc.contributor.authorYoung Ik Lee-
dc.date.accessioned2017-04-19T09:05:05Z-
dc.date.available2017-04-19T09:05:05Z-
dc.date.issued2006-
dc.identifier.issn0166-3542-
dc.identifier.uri10.1016/j.antiviral.2006.04.006ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/7571-
dc.description.abstractThe aim of this study is to characterize the role of ellagic acid, a flavonoid from a medicinal herb which blocks HBeAg secretion in a HBV infected cell line and in HBeAg transgenic mice, in immune tolerance in chronic HBV infection. Using the mouse strain C57ML/6, HBeAg-producing transgenic mice (HBeAg-Tg), under the control of metal ion-inducible promoter were generated. The effect on immune tolerance of HBeAg-Tg and the release of immune tolerance by the inhibitor of HBeAg secretion, ellagic acid, was tested using T/B cell proliferation, HBeAg/HBeAb production, cytotoxic T-lymphocyte (CTL) and cytokine assays. C57ML/6 based HBeAg-producing HBeAg-Tg mice were tolerant to HBeAg at the T and B-cell level, did not produce antibodies to HBeAg in vivo and in vitro, produced minimal levels of cytokines (IL-4 and IFN-gamma) and decreased CTL responses, while feeding mice with ellagic acid (5 mg/kg body weight) blocked the immune tolerance caused by HBeAg. Our results suggest that host immune tolerance induced by HBeAg during HBV infection, a viral strategy to guarantee HBV infection, can be overcome by ellagic acid, thus it can be used as a therapeutic for HBV-carriers.-
dc.publisherElsevier-
dc.titleThe flavonoid ellagic acid from a medicinal herb inhibits host immune tolerance induced by the hepatitis B virus-e antigen-
dc.title.alternativeThe flavonoid ellagic acid from a medicinal herb inhibits host immune tolerance induced by the hepatitis B virus-e antigen-
dc.typeArticle-
dc.citation.titleAntiviral Research-
dc.citation.number2-
dc.citation.endPage106-
dc.citation.startPage100-
dc.citation.volume72-
dc.contributor.affiliatedAuthorYoung Ik Lee-
dc.contributor.alternativeName강은화-
dc.contributor.alternativeName권태영-
dc.contributor.alternativeName오구택-
dc.contributor.alternativeName박응필-
dc.contributor.alternativeName박성일-
dc.contributor.alternativeName박성규-
dc.contributor.alternativeName이영익-
dc.identifier.bibliographicCitationAntiviral Research, vol. 72, no. 2, pp. 100-106-
dc.identifier.doi10.1016/j.antiviral.2006.04.006-
dc.subject.keywordanti-HBV infection-
dc.subject.keywordellagic acid-
dc.subject.keywordhepatitis B virus-e antigen-
dc.subject.keywordimmune tolerance-
dc.subject.localanti-HBV infection-
dc.subject.localEllagic acid-
dc.subject.localellagic acid-
dc.subject.localHepatitis B virus-e antigen-
dc.subject.localhepatitis B virus-e antigen-
dc.subject.localimmune tolerance-
dc.description.journalClassY-
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