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The aim of this study was to investigate if cellular immune responses are modified by <jats:styled-content style=\"fixed-case\">HCV<\/jats:styled-content> persistence in <jats:styled-content style=\"fixed-case\">PBMC<\/jats:styled-content>s.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p><jats:styled-content style=\"fixed-case\">HCV<\/jats:styled-content>\u2010specific <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>4<jats:sup>+<\/jats:sup> and <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>8<jats:sup>+<\/jats:sup> T\u2010cell responses against six <jats:styled-content style=\"fixed-case\">HCV<\/jats:styled-content> peptides, situated within the non\u2010structural (<jats:styled-content style=\"fixed-case\">NS<\/jats:styled-content>) proteins <jats:styled-content style=\"fixed-case\">NS<\/jats:styled-content>3, <jats:styled-content style=\"fixed-case\">NS<\/jats:styled-content>4b and <jats:styled-content style=\"fixed-case\">NS<\/jats:styled-content>5b, were measured by flow cytometry\u2010through intracellular detection of gamma interferon (<jats:styled-content style=\"fixed-case\">IFN<\/jats:styled-content>\u2010\u03b3) or interleukin 4 (<jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u20104) and <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>69 expression\u2010 in 27 sustained virological responders (<jats:styled-content style=\"fixed-case\">SVR<\/jats:styled-content>): 13 with and 14 without occult <jats:styled-content style=\"fixed-case\">HCV<\/jats:styled-content> infection in <jats:styled-content style=\"fixed-case\">PBMC<\/jats:styled-content>s, detected by strand\u2010specific real\u2010time <jats:styled-content style=\"fixed-case\">PCR<\/jats:styled-content>. Ten healthy individuals and 14 chronically infected patients with viraemia, were included as controls.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p><jats:styled-content style=\"fixed-case\">SVR<\/jats:styled-content> without occult infection showed a higher percentage of activated <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>4<jats:sup>+<\/jats:sup> cells against peptides belonging to <jats:styled-content style=\"fixed-case\">NS<\/jats:styled-content>3 (p124, p153) and <jats:styled-content style=\"fixed-case\">NS<\/jats:styled-content>5b (p257, p294), activated <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>8<jats:sup>+<\/jats:sup> cells against <jats:styled-content style=\"fixed-case\">NS<\/jats:styled-content>3 (p124, p153, p158) and <jats:styled-content style=\"fixed-case\">NS<\/jats:styled-content>5b\u2010p294, as well as an elevated percentage of <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>4<jats:sup>+<\/jats:sup> cells releasing <jats:styled-content style=\"fixed-case\">IFN<\/jats:styled-content>\u2010\u03b3\u00a0+\u00a0<jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u20104 against <jats:styled-content style=\"fixed-case\">NS<\/jats:styled-content>3\u2010p153, and by <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>8<jats:sup>+<\/jats:sup> cells against <jats:styled-content style=\"fixed-case\">NS<\/jats:styled-content>3 (p124, p153). <jats:styled-content style=\"fixed-case\">SVR<\/jats:styled-content> without occult infection showed a higher percentage of activation and release of <jats:styled-content style=\"fixed-case\">IFN<\/jats:styled-content>\u2010\u03b3\u00a0+\u00a0<jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u20104 by both cell subpopulations than the two group of controls, in contrast to <jats:styled-content style=\"fixed-case\">SVR<\/jats:styled-content> with occult infection.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusion<\/jats:title><jats:p>The lower <jats:styled-content style=\"fixed-case\">HCV<\/jats:styled-content>\u2010specific T\u2010cell response found in <jats:styled-content style=\"fixed-case\">SVR<\/jats:styled-content> with occult infection indicates that the immune response may be impaired when the virus persists in <jats:styled-content style=\"fixed-case\">PBMC<\/jats:styled-content>s.<\/jats:p><\/jats:sec>","DOI":"10.1111\/liv.12320","type":"journal-article","created":{"date-parts":[[2013,9,11]],"date-time":"2013-09-11T11:51:19Z","timestamp":1378900279000},"source":"Crossref","is-referenced-by-count":8,"title":["Hepatitis C virus\u2010specific cellular immune responses in sustained virological responders with viral persistence in peripheral blood mononuclear cells"],"prefix":"10.1111","volume":"34","author":[{"given":"Mar\u00eda 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