The kinetics of serum viral responses and acute liver injury were studied during neonatal woodchuck hepatitis virus (WHV) infection in relation to the chronic or resolved outcome. The mean concentrations of serum WHV DNA and surface antigen were significantly higher by week 10 post infection in chronic infections compared to resolving infections, and diverged even further by the time of peak viral load development in serum (week 12). After week 12,these viral markers were detected less frequently with time and at lower concentrations in the resolved outcome. In both outcomes, mean serum activities of hepatic enzymes became increased significantly above baseline by weeks 10-12, peaked at week 14, and normalized by weeks 20-22, thus indicating transient acute liver injury. The increasing liver injury responses were comparable between outcomes at week 12, when serum viral load was markedly higher in the developing chronic infections. This suggested a deficiency in early non-cytolytic control of infection in the chronic outcome. At week 14, liver injury was significantly greater in the resolved outcome and associated with higher mean Fas ligand (FasL) and perforin messenger RNAs (mRNAs) in liver compared to the chronic outcome. This indicated greater immune-mediated killing of infected hepatocytes during resolution. Thus, chronicity as an outcome of neonatal WHV infection develops relatively early during the acute phase of infection due to reduced immune-mediated clearance of infected hepatocytes by both cytolytic and non-cytolytic processes. (C) 2004 Wiley-Liss, Inc.
机构:
Scottish Liver Transplant Unit,Royal Infirmary of Edinburgh,Edinburgh,EH16 4SA,United KingdomDepartment of Life Sciences,Glasgow Caledonian University,Glasgow,G4 0BA,United Kingdom
Kenneth J Simpson
Darren G Craig
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Scottish Liver Transplant Unit,Royal Infirmary of Edinburgh,Edinburgh,EH16 4SA,United KingdomDepartment of Life Sciences,Glasgow Caledonian University,Glasgow,G4 0BA,United Kingdom
Darren G Craig
Christopher Bellamy
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Department of Pathology,University of Edinburgh,Edinburgh,EH16 4SB,United Kingdom
4. Gastrointestinal Unit,Royal Cornwall Hospital,and European Centre for the Environment and Human Health,University Department of Life Sciences,Glasgow Caledonian University,Glasgow,G4 0BA,United Kingdom
Christopher Bellamy
Janice Davidson
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Scottish Liver Transplant Unit,Royal Infirmary of Edinburgh,Edinburgh,EH16 4SA,United KingdomDepartment of Life Sciences,Glasgow Caledonian University,Glasgow,G4 0BA,United Kingdom
Janice Davidson
Harry R Dalton
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机构:Department of Life Sciences,Glasgow Caledonian University,Glasgow,G4 0BA,United Kingdom
Harry R Dalton
Linda Scobie
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机构:Department of Life Sciences,Glasgow Caledonian University,Glasgow,G4 0BA,United Kingdom
机构:
Royal Infirm Edinburgh NHS Trust, Scottish Liver Transplant Unit, Edinburgh EH16 4SA, Midlothian, ScotlandGlasgow Caledonian Univ, Dept Life Sci, Glasgow G4 0BA, Lanark, Scotland
Davidson, Janice
Dalton, Harry R.
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Univ Exeter, Med Sch, Royal Cornwall Hosp, Gastrointestinal Unit, Truro TR1 3HD, England
Univ Exeter, Med Sch, European Ctr Environm & Human Hlth, Truro TR1 3HD, EnglandGlasgow Caledonian Univ, Dept Life Sci, Glasgow G4 0BA, Lanark, Scotland