Immune-based therapy for chronic hepatitis C

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dc.contributor.authorChang, Dong-Yeopko
dc.contributor.authorShin, Eui-Cheolko
dc.date.accessioned2009-11-30T08:34:27Z-
dc.date.available2009-11-30T08:34:27Z-
dc.date.created2012-02-06-
dc.date.created2012-02-06-
dc.date.issued2009-07-
dc.identifier.citationJOURNAL OF LEUKOCYTE BIOLOGY, v.86, no.1, pp.33 - 39-
dc.identifier.issn0741-5400-
dc.identifier.urihttp://hdl.handle.net/10203/13708-
dc.description.abstractChronic, persistent HCV infection is a public health issue. It often progresses to life-threatening complications, including liver cirrhosis and hepatocellular carcinoma. The current standard therapy is a combination of pegylated IFN-alpha and ribavirin. This therapy results in a sustained virologic response in only 50% of patients infected with HCV genotype 1 and is often accompanied with substantial side-effects. Therefore, it is imperative to develop novel therapies with higher efficacy and less substantial side-effects. Impaired immune responses to HCV are key features of chronic HCV infection; thus, intervention strategies typically involve boosting the immune responses against HCV. These immune-based therapies for chronic HCV infection include therapeutic vaccines, antagonists of T cell inhibitory factors, anti-HCV neutralizing antibodies, cytokines, and agonists for TLRs. Currently, various types of immune-based therapies are under development that might be used as a monotherapy or in combination with other antiviral drugs for the treatment of chronic HCV infection. J. Leukoc. Biol. 86: 33-39; 2009.-
dc.languageEnglish-
dc.language.isoen_USen
dc.publisherFEDERATION AMER SOC EXP BIOL-
dc.subjectCHRONIC VIRAL-INFECTION-
dc.subjectT-CELL RESPONSES-
dc.subjectRECOMBINANT HUMAN INTERLEUKIN-12-
dc.subjectNECROSIS-FACTOR-ALPHA-
dc.subjectVIRUS-INFECTION-
dc.subjectDOUBLE-BLIND-
dc.subjectGAMMA-INTERFERON-
dc.subjectPD-1 EXPRESSION-
dc.subjectMONOCLONAL-ANTIBODY-
dc.subjectCONTROLLED TRIAL-
dc.titleImmune-based therapy for chronic hepatitis C-
dc.typeArticle-
dc.identifier.wosid000267488700006-
dc.identifier.scopusid2-s2.0-68849127031-
dc.type.rimsART-
dc.citation.volume86-
dc.citation.issue1-
dc.citation.beginningpage33-
dc.citation.endingpage39-
dc.citation.publicationnameJOURNAL OF LEUKOCYTE BIOLOGY-
dc.identifier.doi10.1189/JLB.1208772-
dc.embargo.liftdate9999-12-31-
dc.embargo.terms9999-12-31-
dc.contributor.localauthorShin, Eui-Cheol-
dc.type.journalArticleReview-
dc.subject.keywordAuthorHCV-
dc.subject.keywordAuthorimmunotherapy-
dc.subject.keywordAuthorT cell-
dc.subject.keywordAuthorcytokine-
dc.subject.keywordPlusCHRONIC VIRAL-INFECTION-
dc.subject.keywordPlusT-CELL RESPONSES-
dc.subject.keywordPlusRECOMBINANT HUMAN INTERLEUKIN-12-
dc.subject.keywordPlusNECROSIS-FACTOR-ALPHA-
dc.subject.keywordPlusVIRUS-INFECTION-
dc.subject.keywordPlusDOUBLE-BLIND-
dc.subject.keywordPlusGAMMA-INTERFERON-
dc.subject.keywordPlusPD-1 EXPRESSION-
dc.subject.keywordPlusMONOCLONAL-ANTIBODY-
dc.subject.keywordPlusCONTROLLED TRIAL-
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