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Hepatic and extrahepatic HCV RNA strands in chronic hepatitis C: Different patterns of response to interferon treatment

Authors

  • Beatriz Gil,

    1. Department of Internal Medicine, Center for Biomedical Research, School of Medicine, University of Navarra, 31080 Pamplona, Spain
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  • Cheng Qian,

    1. Department of Internal Medicine, Center for Biomedical Research, School of Medicine, University of Navarra, 31080 Pamplona, Spain
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  • Jose I. Riezu-Boj,

    1. Department of Internal Medicine, Center for Biomedical Research, School of Medicine, University of Navarra, 31080 Pamplona, Spain
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  • Maria P. Civeira,

    1. Department of Internal Medicine, Center for Biomedical Research, School of Medicine, University of Navarra, 31080 Pamplona, Spain
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  • Jesús Prieto M.D.

    Corresponding author
    1. Department of Internal Medicine, Center for Biomedical Research, School of Medicine, University of Navarra, 31080 Pamplona, Spain
    • Departamento de Medicina Interna, Centro de Investigaciones Biomedicas, Clinica Universitaria, Facultad de Medicina, c/Pio XII, 36, 31080 Pamplona, Spain
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Abstract

We investigated the presence of positive (genomic) and negative (replicative intermediate) hepatitis C virus RNA strands in liver, peripheral mononuclear cells and serum from patients with chronic hepatitis C using a selective and semiquantitative polymerase chain reaction procedure. Negative and positive hepatitis C virus RNA strands were present in liver, serum and lymphoid cells in all untreated patients and in all those who did not respond to interferon therapy. In the latter group of patients, the titers of RNA strands in the liver and peripheral mononuclear cells at the end of the treatment were similar to those encountered in untreated patients, but the serum titers were about 100 times lower than pretreatment values. In patients who responded to interferon with normalization of serum aminotransferase levels (n = 10), the rate of detection and the titer of the two viral strands in liver, serum and mononuclear cells were markedly decreased at the end of the therapy. In the six responders who did not relapse after interferon withdrawal, both hepatitis C virus RNA strands were absent from the liver, serum and lymphoid cells. By contrast, the positive RNA strand was present in liver cells, mononuclear cells or both at the end of therapy in all patients who experienced posttherapy relapse. In conclusion, our results indicate that interferon can clear hepatitis C virus from hepatic and extrahepatic sites only in responder patients. Disappearance of genomic hepatitis C virus RNA from the liver and from mononuclear cells may predict complete response without posttherapy relapse. (HEPATOLOGY 1993;18:1050-1054).

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