Increases in intrahepatic CD68 positive cells, MAC387 positive cells, and proinflammatory cytokines (particularly interleukin 18) in chronic hepatitis C infection

Gut. 2000 Feb;46(2):260-9. doi: 10.1136/gut.46.2.260.

Abstract

Background: Upregulation of Th1 associated intrahepatic cytokines in chronic hepatitis C virus (HCV) infection should lead to a significant non-specific cellular immune response, a prerequisite for viral clearance. However, to date, the role of this non-specific response in HCV has been understudied.

Aims: To analyse the intrahepatic macrophage activity in chronic HCV infection by immunostaining and by quantitation of cytokine mRNA.

Methods: HCV positive liver tissues (chronic hepatitis, n=10; cirrhosis, n=5) were immunostained for CD68, MAC387, and semiquantitated by polymerase chain reaction for intrahepatic cytokine mRNAs (interferon gamma (IFNgamma), interleukin 1beta (IL-1beta), IL-6, IL-18, tumour necrosis factor alpha (TNFalpha), and macrophage inflammatory protein 1beta (MIP1beta)). HCV negative normal liver tissues (for cytokines, n=6; for immunostaining, n=5) were included as controls.

Results: MAC387(+) cells were focally increased in areas of erosion at the limiting plate while lobular staining was minimal. CD68(+) staining was diffuse in both portal (increased in HCV) and lobular areas. The portal tract (mean) density of CD68(+) and MAC387(+) cells was significantly increased in patients with HCV compared with normal tissue. IFNgamma and IL-18 mRNA levels were highly correlated and significantly upregulated in chronic hepatitis and cirrhotic tissue versus controls. TNFalpha mRNA was upregulated in chronic hepatitis without cirrhosis, while IL-6 mRNA was significantly downregulated. IL-1beta, IL-6, and MIP1beta mRNA levels were significantly correlated with portal tract MAC387(+) cell density.

Conclusions: The significant upregulation of IFNgamma and IL-18 mRNA and significant correlations between IFNgamma and other proinflammatory cytokines, suggest a Th1/cell mediated intrahepatic immune response in chronic HCV infection. However, further clarification of the cellular sources of these cytokines is required.

MeSH terms

  • Adult
  • Antigens, CD / immunology*
  • Antigens, Differentiation, Myelomonocytic / immunology*
  • Biomarkers / analysis
  • Chemokine CCL4
  • Female
  • Hepatitis C, Chronic / immunology*
  • Humans
  • Interferon-gamma / genetics
  • Interleukin-1 / genetics
  • Interleukin-18 / genetics*
  • Interleukin-6 / genetics
  • Liver / immunology*
  • Macrophage Inflammatory Proteins / genetics
  • Macrophages / immunology
  • Male
  • Middle Aged
  • Reverse Transcriptase Polymerase Chain Reaction
  • Statistics, Nonparametric
  • Th1 Cells / immunology
  • Tumor Necrosis Factor-alpha / genetics

Substances

  • Antigens, CD
  • Antigens, Differentiation, Myelomonocytic
  • Biomarkers
  • CD68 antigen, human
  • Chemokine CCL4
  • Interleukin-1
  • Interleukin-18
  • Interleukin-6
  • Macrophage Inflammatory Proteins
  • Tumor Necrosis Factor-alpha
  • Interferon-gamma