Primary biliary cirrhosis-related autoantibodies in a large cohort of italian patients with systemic sclerosis

J Rheumatol. 2011 Oct;38(10):2180-5. doi: 10.3899/jrheum.110167. Epub 2011 Sep 15.

Abstract

Objective: To analyze the prevalence, associations, and fine specificity of autoantibodies to primary biliary cirrhosis (PBC)-associated antigens (MIT3, Sp100, and gp210) in a cohort of Italian patients with systemic sclerosis (SSc).

Methods: Sera samples from 201 patients with SSc were tested for antibodies to MIT3, gp210, and Sp100 by ELISA (the PBC screen). Anti-MIT3-positive sera were studied for IgG or IgA isotypes. All sera were analyzed by indirect immunofluorescence on HEp-2 cells and on rodent kidney/stomach/liver tissue sections in order to detect antinuclear and antimitochondrial antibodies (AMA). SSc was selected by American College of Rheumatology criteria and classified based on LeRoy's criteria.

Results: Forty-three (21.4%) sera samples were positive for PBC screen antibodies. Anti-MIT3 antibodies were detected in 36 samples, anti-Sp100 in 5, and anti-gp210 in 1 sample. The other 3 PBC screen-positive samples showed no specificity for the single antigens. PBC screen-positive patients more frequently showed a limited cutaneous SSc subtype (p = 0.04), anticentromere antibodies (ACA; p = 0.0013), elevated alkaline phosphatase (ALP) (p < 0.0001), PBC (p = 0.002), and AMA (p = 0.008). Teleangiectasia and calcinosis were less frequent in this group of patients. IgG+IgA anti-MIT3-positive patients had higher prevalence of AMA (p = 0.0035), diagnosis of PBC (p = 0.014), and increased ALP (p = 0.039), all considered biochemical markers of severe liver disease.

Conclusion: PBC screen antibodies were detected in 20% of patients with SSc, strongly associated with ACA. ACA+/PBC screen+ patients had higher risk of developing PBC or elevation of ALP.

MeSH terms

  • Adult
  • Aged
  • Antigens, Nuclear / immunology
  • Autoantibodies / immunology*
  • Autoantigens / immunology
  • Female
  • Humans
  • Italy
  • Liver Cirrhosis, Biliary / diagnosis*
  • Liver Cirrhosis, Biliary / immunology
  • Male
  • Middle Aged
  • Nuclear Pore Complex Proteins / immunology
  • Predictive Value of Tests
  • Recombinant Fusion Proteins / immunology
  • Scleroderma, Systemic / immunology*
  • Sensitivity and Specificity

Substances

  • Antigens, Nuclear
  • Autoantibodies
  • Autoantigens
  • MIT3 fusion protein
  • NUP210 protein, human
  • Nuclear Pore Complex Proteins
  • Recombinant Fusion Proteins
  • SP100 protein, human