CD8+ T-cell interaction with HCV replicon cells: evidence for both cytokine- and cell-mediated antiviral activity

Hepatology. 2003 Jun;37(6):1335-42. doi: 10.1053/jhep.2003.50207.

Abstract

The interaction between the host immune response and infected hepatocytes plays a central role in the pathogenesis of hepatitis C virus (HCV). The lack of a suitable animal or in vitro model has hindered our understanding of the host T-cell/HCV interaction. Our aim was to develop an in vitro model to study the mechanisms of HCV-specific T-cell-mediated antiviral and cytolytic function. The HCV replicon was HLA typed and lymphocytes were obtained from an HLA class I-matched subject. CD8(+) T cells were expanded with 2 HCV-specific/HLA-restricted peptides for NS3. Lymphocyte preparations were cocultured with HCV replicon (FCA1) and control (Huh7) cells labeled with (51)Cr. After a 48-hour incubation, the cells were harvested for RNA extraction. Standard blocking assays were performed in the presence of anti-interferon gamma (IFN-gamma), anti-tumor necrosis factor alpha (TNF-alpha), and anti-FasL. Cytolytic activity was measured by (51)Cr release. HCV replicon cells express homozygous HLA-A11 alleles and present HCV nonstructural proteins. HCV-specific expansion of CD8(+) cells led to a 10-fold decrease in HCV replication by Northern blot analysis and 21% specific lysis of FCA1 cells (compared with 2% of control Huh7 cells). Twenty percent of this antiviral activity was independent of T-cell binding, suggesting cytokine-mediated antiviral activity. The CD8(+) antiviral effect was markedly reduced by blocking either IFN-gamma or FasL but was unaffected by blocking TNF-alpha. In conclusion, HCV-specific CD8(+) cells inhibit viral RNA replication by cytokine-mediated and direct cytolytic effects. This T-cell/HCV subgenomic replicon system represents a model for the investigation of CD8 cell interaction with HCV-infected hepatocytes.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Antibodies / pharmacology
  • Antibodies, Viral / immunology
  • Antibody Formation
  • CD8-Positive T-Lymphocytes / immunology
  • CD8-Positive T-Lymphocytes / physiology*
  • Cell Communication*
  • Cytokines / physiology*
  • Fas Ligand Protein
  • HLA Antigens / analysis
  • HLA Antigens / metabolism
  • Hepacivirus / genetics
  • Hepacivirus / immunology
  • Hepacivirus / physiology*
  • Humans
  • Interferon-gamma / immunology
  • Liver
  • Lymph Nodes / cytology
  • Membrane Glycoproteins / immunology
  • Replicon*
  • Tumor Cells, Cultured
  • Tumor Necrosis Factor-alpha / immunology

Substances

  • Antibodies
  • Antibodies, Viral
  • Cytokines
  • FASLG protein, human
  • Fas Ligand Protein
  • HLA Antigens
  • Membrane Glycoproteins
  • Tumor Necrosis Factor-alpha
  • Interferon-gamma