Expression of leukocyte adhesion molecules in the liver of patients with chronic hepatitis B virus infection

Gastroenterology. 1991 Mar;100(3):749-55. doi: 10.1016/0016-5085(91)80021-z.

Abstract

Virus-specific T-cell responses are believed to be involved in the pathogenesis of liver cell injury secondary to hepatitis B virus infection. In this study, liver biopsy specimens from patients with chronic hepatitis B virus infection were analyzed for expression of two major pathways of adhesion used by cytotoxic T cells to interact with target cells. The lymphocyte function-associated antigen 3 was found preferentially expressed on hepatocytes of patients with active hepatitis B virus replication, whereas the expression of the intercellular adhesion molecule 1 on hepatocytes seemed more closely related with inflammatory activity. Adhesion molecules were also highly expressed on T lymphocytes found in areas of piecemeal and spotty necrosis, indicating the presence of antigen-specific "memory" T cells at the site of hepatocellular injury. This study suggests that the expression of the lymphocyte function-associated antigen 3 on hepatocytes may be important for viral elimination. The coordinate expression of the intercellular adhesion molecule 1 may regulate inflammatory response and enhance viral antigen presentation to T cells. Conversely, the absence of hepatocyte adhesion molecules might be a favorable factor for viral persistence.

MeSH terms

  • Antigens, Surface / analysis*
  • CD58 Antigens
  • Cell Adhesion Molecules / physiology*
  • Chronic Disease
  • Hepatitis B / immunology*
  • Hepatitis B Surface Antigens / blood
  • Humans
  • Liver / cytology
  • Liver / immunology*
  • Liver / pathology
  • Lymphocyte Function-Associated Antigen-1 / analysis*
  • Membrane Glycoproteins / analysis*
  • T-Lymphocytes / chemistry

Substances

  • Antigens, Surface
  • CD58 Antigens
  • Cell Adhesion Molecules
  • Hepatitis B Surface Antigens
  • Lymphocyte Function-Associated Antigen-1
  • Membrane Glycoproteins