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The frequency of <jats:styled-content style=\"fixed-case\">MDSC<\/jats:styled-content> denoted here as <jats:styled-content style=\"fixed-case\">L<\/jats:styled-content>in<jats:sup>\u2212\/low<\/jats:sup><jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>33<jats:sup>+<\/jats:sup><jats:styled-content style=\"fixed-case\">HLA\u2010DR<\/jats:styled-content><jats:sup>\u2212<\/jats:sup> was investigated in hepatocellular carcinoma (<jats:styled-content style=\"fixed-case\">HCC<\/jats:styled-content>) patients. The clinical relevance of <jats:styled-content style=\"fixed-case\">MDSC<\/jats:styled-content> and patients' characteristics were examined. Also, <jats:styled-content style=\"fixed-case\">MDSC<\/jats:styled-content>\u2010related immune regulatory pathways in these patients were discussed.<\/jats:p><\/jats:sec><jats:sec><jats:title>Methods<\/jats:title><jats:p>The quantity of <jats:styled-content style=\"fixed-case\">MDSC<\/jats:styled-content> was tested in peripheral blood of patients with <jats:styled-content style=\"fixed-case\">HCC<\/jats:styled-content> (<jats:italic>n<\/jats:italic>\u2009=\u200963) and healthy donors (<jats:italic>n<\/jats:italic>\u2009=\u200956). The expressions of interferon (<jats:styled-content style=\"fixed-case\">IFN<\/jats:styled-content>)\u2010\u03b3, vascular endothelial growth factor (<jats:styled-content style=\"fixed-case\">VEGF<\/jats:styled-content>), cyclooxygenase (<jats:styled-content style=\"fixed-case\">COX<\/jats:styled-content>)\u20102, matrix metalloproteinase (<jats:styled-content style=\"fixed-case\">MMP<\/jats:styled-content>)\u201013, nitric oxide synthase (<jats:styled-content style=\"fixed-case\">NOS<\/jats:styled-content>)\u20102 and arginase (<jats:styled-content style=\"fixed-case\">ARG<\/jats:styled-content>)\u20101 were analyzed. Co\u2010culturing with anti\u2010<jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>3\/<jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>28\u2010stimulated T lymphocytes was used to determine the suppressive effect of <jats:styled-content style=\"fixed-case\">MDSC<\/jats:styled-content> on the T lymphocytes.<\/jats:p><\/jats:sec><jats:sec><jats:title>Results<\/jats:title><jats:p>Patients with treatment\u2010naive <jats:styled-content style=\"fixed-case\">HCC<\/jats:styled-content> had an increased subpopulation of <jats:styled-content style=\"fixed-case\">L<\/jats:styled-content>in<jats:sup>\u2212\/low<\/jats:sup><jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>33<jats:sup>+<\/jats:sup><jats:styled-content style=\"fixed-case\">HLA\u2010DR<\/jats:styled-content><jats:sup>\u2212<\/jats:sup> cells in the peripheral blood mononuclear cells (<jats:styled-content style=\"fixed-case\">PBMC<\/jats:styled-content>) with characteristics of <jats:styled-content style=\"fixed-case\">MDSC<\/jats:styled-content> and associated to the stage (<jats:italic>P<\/jats:italic>\u2009=\u20090.0004). Patients with splenomegaly had a higher frequency of circulating <jats:styled-content style=\"fixed-case\">MDSC<\/jats:styled-content>. Also, <jats:styled-content style=\"fixed-case\">COX<\/jats:styled-content>\u20102, <jats:styled-content style=\"fixed-case\">MMP<\/jats:styled-content>\u201013 and <jats:styled-content style=\"fixed-case\">VEGF<\/jats:styled-content> were expressed differently associated with the alteration of <jats:styled-content style=\"fixed-case\">MDSC<\/jats:styled-content>.<\/jats:p><\/jats:sec><jats:sec><jats:title>Conclusion<\/jats:title><jats:p>Our study provides evidence showing an increased population of <jats:styled-content style=\"fixed-case\">L<\/jats:styled-content>in<jats:sup>\u2212\/low<\/jats:sup><jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>33<jats:sup>+<\/jats:sup><jats:styled-content style=\"fixed-case\">HLA\u2010DR<\/jats:styled-content><jats:sup>\u2212<\/jats:sup> <jats:styled-content style=\"fixed-case\">MDSC<\/jats:styled-content> in the peripheral blood of <jats:styled-content style=\"fixed-case\">HCC<\/jats:styled-content> patients. Our data also suggest that <jats:styled-content style=\"fixed-case\">MMP<\/jats:styled-content>\u201013 and <jats:styled-content style=\"fixed-case\">COX<\/jats:styled-content>\u20102 in <jats:styled-content style=\"fixed-case\">PBMC<\/jats:styled-content> may play a new important role companied with <jats:styled-content style=\"fixed-case\">MDSC<\/jats:styled-content> in <jats:styled-content style=\"fixed-case\">HCC<\/jats:styled-content> patients.<\/jats:p><\/jats:sec>","DOI":"10.1111\/hepr.12167","type":"journal-article","created":{"date-parts":[[2013,5,22]],"date-time":"2013-05-22T12:03:01Z","timestamp":1369224181000},"page":"639-650","source":"Crossref","is-referenced-by-count":62,"title":["Increased circulating <scp>L<\/scp>in<sup>\u2212\/low<\/sup><scp>CD<\/scp>33<sup>+<\/sup><scp>HLA\u2010DR<\/scp><sup>\u2212<\/sup> myeloid\u2010derived suppressor cells in hepatocellular carcinoma 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