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dc.creatorLarrea, E. (Esther)-
dc.creatorRiezu-Boj, J.I. (José Ignacio)-
dc.creatorGil-Guerrero, L. (Lucía)-
dc.creatorCasares, N. (Noelia)-
dc.creatorAldabe, R. (Rafael)-
dc.creatorSarobe, P. (Pablo)-
dc.creatorCiveira, M.P. (María Pilar)-
dc.creatorHeeney, J.L. (Jonathan L.)-
dc.creatorRollier, C.S. (Christine S.)-
dc.creatorVerstrepen, B.E. (Babs E.)-
dc.date.accessioned2012-04-04T12:16:46Z-
dc.date.available2012-04-04T12:16:46Z-
dc.date.issued2007-
dc.identifier.citationLarrea E, Riezu-Boj JI, Gil-Guerrero L, Casares N, Aldabe R, Sarobe P, et al. Upregulation of indoleamine 2,3-dioxygenase in hepatitis C virus infection. J Virol 2007 Apr;81(7):3662-3666.es_ES
dc.identifier.issn1098-5514-
dc.identifier.urihttps://hdl.handle.net/10171/21602-
dc.description.abstractIndoleamine 2,3-dioxygenase (IDO) is induced by proinflammatory cytokines and by CTLA-4-expressing T cells and constitutes an important mediator of peripheral immune tolerance. In chronic hepatitis C, we found upregulation of IDO expression in the liver and an increased serum kynurenine/tryptophan ratio (a reflection of IDO activity). Huh7 cells supporting hepatitis C virus (HCV) replication expressed higher levels of IDO mRNA than noninfected cells when stimulated with gamma interferon or when cocultured with activated T cells. In infected chimpanzees, hepatic IDO expression decreased in animals that cured the infection, while it remained high in those that progressed to chronicity. For both patients and chimpanzees, hepatic expression of IDO and CTLA-4 correlated directly. Induction of IDO may dampen T-cell reactivity to viral antigens in chronic HCV infectiones_ES
dc.language.isoenges_ES
dc.publisherAmerican Society for Microbiologyes_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.subjectGene Expression Regulation, Enzymologices_ES
dc.subjectHepatitis C/enzymologyes_ES
dc.subjectIndoleamine-Pyrrole 2,3,-Dioxygenase/metabolismes_ES
dc.titleUpregulation of indoleamine 2,3-dioxygenase in hepatitis C virus infectiones_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherversionhttp://jvi.asm.org/content/81/7/3662es_ES
dc.type.driverinfo:eu-repo/semantics/articlees_ES

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