High levels of soluble CTLA-4 are present in anti-mitochondrial antibody positive, but not in antibody negative patients with primary biliary cirrhosis

PLoS One. 2014 Nov 10;9(11):e112509. doi: 10.1371/journal.pone.0112509. eCollection 2014.

Abstract

Primary biliary cirrhosis (PBC) is a chronic autoimmune cholestatic liver disease frequently characterized by anti-mitochondrial autoantibodies (AMA). A minority of patients are AMA-negative. Cytotoxic-T-Lymphocyte-Antigen-4 (CTLA-4) is a surface molecule expressed on activated T-cells delivering a critical negative immunoregulatory signal. A soluble form of CTLA-4 (sCTLA-4) has been detected at high concentrations in several autoimmune diseases, and its possible functional meaning has been suggested. We aimed to evaluate sCTLA-4 concentration in sera of patients with PBC and to correlate it to immunological abnormalities associated with the disease. Blood samples were collected from 82 PBC-patients diagnosed according to international criteria (44 AMA-positive/MIT3-positive and 38 AMA-negative-MIT3-negative), and 65 controls. sCTLA-4 levels were evaluated by ELISA and Western blot. Increased sCTLA-4 concentrations were found in all AMA-positive PBC-patients, but in none of the AMA-negative ones, nor in normal controls or in controls with unrelated liver diseases. sCTLA-4 presence was associated with autoantibodies against MIT3, but not with nuclear autoantibodies (sp100, gp210). This is the first study to demonstrate that levels of sCTLA-4 are elevated in sera of PBC patients. However, they are clearly restricted to patients with AMA positivity, suggesting an immunological difference with respect to AMA-negative ones.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Antigens, Nuclear / metabolism
  • Autoantibodies / immunology*
  • Autoantigens / metabolism
  • CTLA-4 Antigen / blood
  • CTLA-4 Antigen / metabolism*
  • Case-Control Studies
  • Female
  • Humans
  • Liver Cirrhosis, Biliary / blood
  • Liver Cirrhosis, Biliary / immunology*
  • Liver Cirrhosis, Biliary / pathology
  • Male
  • Middle Aged
  • Mitochondria / immunology*
  • Nuclear Pore Complex Proteins / metabolism
  • Recombinant Fusion Proteins / immunology
  • Up-Regulation

Substances

  • Antigens, Nuclear
  • Autoantibodies
  • Autoantigens
  • CTLA-4 Antigen
  • CTLA4 protein, human
  • MIT3 fusion protein
  • NUP210 protein, human
  • Nuclear Pore Complex Proteins
  • Recombinant Fusion Proteins
  • SP100 protein, human

Grants and funding

This work was funded by University of Genova, Italy (PRA2012). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.