Overexpression of MHCII by hepatocytes in alcoholic hepatitis (AH) compared to non-alcoholic steatohepatitis (NASH) and normal controls

Alcohol. 2020 May:84:27-32. doi: 10.1016/j.alcohol.2019.08.008. Epub 2019 Sep 5.

Abstract

Previously we have shown that in autoimmune hepatitis CD4 positive lymphocytes form an immunologic synapse with hepatocytes, leading to gradual diminishing and elimination of the hepatocyte. We wondered whether a similar mechanism may occur in alcoholic hepatitis (AH) and non-alcoholic steatohepatitis (NASH). We conducted immunofluorescence studies of expression of MHCII, the binding partner of CD4, on patient liver biopsies of AH, NASH, and normal controls. In cases of alcoholic hepatitis, there was prominent sinusoidal expression of MHC II; In NASH biopsies there was comparatively lower expression of MHC II, but still more than control tissue. Immunohistochemical stain for CD4 showed CD4 positive lymphocytes closely associated with hepatocytes in AH biopsies. Furthermore, expression levels of the multifunctional cytokine IL-1α was higher in AH compared to NASH and control biopsies. These results underlie the more severe nature of alcoholic hepatitis and underscore the autoimmune mechanisms involved in the liver damage found in alcoholic hepatitis.

Keywords: Alcoholic hepatitis; CD4; Immune synapse; MHCII; Non-alcoholic steatohepatitis.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural

MeSH terms

  • Biopsy
  • CD4-Positive T-Lymphocytes / immunology*
  • Fluorescent Antibody Technique
  • Hepatitis, Alcoholic / immunology*
  • Hepatocytes / pathology*
  • Histocompatibility Antigens Class II / immunology*
  • Humans
  • Immunohistochemistry
  • Interleukin-1alpha / immunology
  • Non-alcoholic Fatty Liver Disease / immunology*

Substances

  • Histocompatibility Antigens Class II
  • IL1A protein, human
  • Interleukin-1alpha