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High inflammatory activity is associated with an increased amount of IFN-γ transcripts in peripheral blood cells of patients with chronic hepatitis C virus infection

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Abstract

The mechanisms underlying the chronic hepatic inflammatory process in hepatitis C virus (HCV) infection are not well understood. Some models of experimentally induced hepatitis point to a role of interferon-gamma (IFN-γ) secreted by liver-infiltrating peripheral blood lymphocytes (PBMC) in mediating hepatocellular injury. In the present study, IFN-γ gene expression was analysed in PBMC and in liver biopsy specimens from patients with chronic HCV infection using a quantitative reverse transcriptase polymerase chain reaction technique. IFN-γ gene expression by PBMC from HCV-infected patients exhibiting elevated serum transaminase activities was found to be increased up to ninefold when compared with (1) healthy individuals, (2) HCV-infected patients exhibiting normal or only slightly elevated serum enzyme activities, or (3) patients with drug-induced elevated serum transaminase activity. A histo-pathological evaluation of liver biopsy sections revealed further that high IFN-γ gene expression by PBMC was associated with a more pronounced degree of inflammatory activity. In individual patients, the expression of IFN-γ by PBMC was shown to parallel closely serum transaminase activities during IFN-α 2a therapy. Moreover, liver biopsy material from patients chronically infected with HCV contained higher amounts of IFN-γ transcripts than liver tissue from patients with liver disorders unrelated to HCV infection or without any liver disease. These data thus demonstrate a close association between the amount of IFN-γ transcripts in PBMC and in liver tissue and the inflammatory activity in chronic HCV infection in man.

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Received: 9 March 1996

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Mihm, S., Hutschenreiter, A., Fayyazi, A. et al. High inflammatory activity is associated with an increased amount of IFN-γ transcripts in peripheral blood cells of patients with chronic hepatitis C virus infection. Med Microbol Immunol 185, 95–102 (1996). https://doi.org/10.1007/s004300050020

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  • DOI: https://doi.org/10.1007/s004300050020

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