Please use this identifier to cite or link to this item: https://saber.ucv.ve/jspui/handle/10872/14870
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dc.contributor.authorToro, Felix-
dc.contributor.authorConesa, Angela-
dc.contributor.authorGarcía, Alexis H.-
dc.contributor.authorBianco Colmenares, Nicolás E.-
dc.contributor.authorDe Sanctis, Juan B.-
dc.date.accessioned2017-03-06T19:06:56Z-
dc.date.available2017-03-06T19:06:56Z-
dc.date.issued1998-08-
dc.identifier.issn0090-1229-
dc.identifier.urihttp://hdl.handle.net/10872/14870-
dc.description.abstractTo evaluate the oxidative burst in hepatitis C virus (HCV) infection, intracellular hydrogen peroxide (H202) production of polymorphonuclear (PMN) cells isolated from 15 chronic HCV-infected patients and 11 controls was assessed by flow cytometry in a time kinetic. Under nonstimulated and phorbol myristate acetate (PMA)-stimulated conditions, H202 production was higher in HCV-infected patients than in controls (P <0.05) at the time points of 20, 30, and 40 min. A positive correlation between H202 production by PMA-stimulated cells and serum levels of alanine aminotransferase and aspartate aminotransferase was found in the HCV-infected patients (r = 0.877, P <0.01 and r = 0.9351, P <0.001, respectively). RT-PCR analysis of purified mononuclear (MN) and PMN cells from HCV-infected patients revealed the presence of HCV RNA in 60% of MN and 27% of PMN cell samples. These results suggest that a functional alteration of PMN cells is manifested in this chronic viral infection which may represent an additional factor in the development of liver lesions.en_US
dc.language.isoenen_US
dc.publisherCLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGYen_US
dc.relation.ispartofseriesVol. 88;No. 2 pp 169-175-
dc.subjectpolymorphonuclear cellsen_US
dc.subjecthepatitis C virus infectionen_US
dc.subjectperoxide productionen_US
dc.subjectflow cytometryen_US
dc.subjectintracellular hydrogenen_US
dc.subjectproduction of polymorphonuclearen_US
dc.titleIncreased peroxide production by polymorphonuclear cells of chronic hepatitis C virus-infected patients.en_US
dc.typeArticleen_US
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