Histological changes in HCV antibody-positive, HCV RNA-negative subjects suggest persistent virus infection

Hepatology. 2008 Dec;48(6):1737-45. doi: 10.1002/hep.22484.

Abstract

It is unclear whether hepatitis C virus (HCV) has been eradicated or persists at a low level in HCV antibody-positive HCV RNA-negative individuals. The natural history and liver histology are not well characterized. One hundred seventy-two HCV antibody-positive, serum HCV RNA-negative patients underwent diagnostic liver biopsy between 1992 and 2000 and were followed a median 7 years (range, 5-12). Patients with any possible cause of liver injury other than HCV were excluded. A single histopathologist scored sections using Ishak criteria. Characterization of the inflammatory infiltrate in selected cases used a novel semiquantitative technique and compared with HCV RNA-positive patients and healthy controls. One hundred two patients were excluded because of a risk factor for liver injury other than HCV. Seventy patients met the study criteria; four (5.7%) became HCV RNA-positive during follow-up. Sixty-six cases remained HCV RNA-negative; five (7.5%) had a normal liver biopsy; 54 (82%) had fibrosis (stage 2 or 3 in 16 (24%)). Nonviremic cases revealed expanded portal tracts (P < 0.05), with fewer CD4+ (P < 0.05) and more CD8+ cells (P < 0.05) than healthy controls, but were indistinguishable from HCV RNA-positive cases for these parameters. Lobular CD4 staining, absent in healthy controls, was noted in both HCV RNA-negative and -positive cases and was more marked in the latter (P < 0.05) with a sinusoidal lining cell distribution.

Conclusion: Nonviremic HCV antibody-positive patients have a liver biopsy that is usually abnormal. Fibrosis was present in most with similar inflammatory infiltrate to viremic cases. The presence of a CD8+ rich inflammatory infiltrate suggests an ongoing immune response in the liver, supporting the view that HCV may persist in the liver in the majority of HCV RNA-negative cases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Alanine Transaminase / metabolism
  • Biopsy
  • CD3 Complex / metabolism
  • CD8-Positive T-Lymphocytes / pathology
  • Case-Control Studies
  • Cohort Studies
  • Disease Progression
  • Female
  • Follow-Up Studies
  • Hepacivirus / genetics*
  • Hepacivirus / immunology
  • Hepatitis C / blood*
  • Hepatitis C / diagnosis
  • Hepatitis C / pathology
  • Hepatitis C Antibodies / blood*
  • Humans
  • Liver / metabolism
  • Liver / pathology
  • Liver / virology
  • Liver Cirrhosis / pathology
  • Male
  • Middle Aged
  • Perforin / metabolism
  • Prognosis
  • RNA, Viral / blood*
  • Virus Replication

Substances

  • CD3 Complex
  • Hepatitis C Antibodies
  • RNA, Viral
  • Perforin
  • Alanine Transaminase