HLA-G expression in the skin of patients with systemic sclerosis

J Rheumatol. 2009 Jun;36(6):1230-4. doi: 10.3899/jrheum.080552. Epub 2009 Apr 15.

Abstract

Objective: To determine HLA-G expression in skin biopsies from patients with systemic sclerosis (SSc), and its association with epidemiological, clinical, and laboratory variables and survival.

Methods: Paraffin-embedded skin biopsies obtained from 21 SSc patients (14 limited SSc, 7 diffuse SSc) and from 28 healthy controls were studied. HLA-G expression was evaluated by immunohistochemistry.

Results: HLA-G molecules were detected in 57% of skin biopsies from patients with SSc (9 from limited SSc, 3 from diffuse SSc), whereas no control sample expressed HLA-G (p=0.000004). In patients, HLA-G molecules were consistently observed within epidermal and some dermal cells. HLA-G expression was associated with a lower frequency of vascular cutaneous ulcers (p=0.0004), telangiectasias (p=0.008), and inflammatory polyarthralgia (p=0.02). After a 15-year followup, SSc patients who exhibited HLA-G survived longer than patients who did not.

Conclusion: HLA-G is expressed in skin biopsies from patients with SSc, and this is associated with a better disease prognosis. This suggests a modulatory role of HLA-G in SSc, as observed in other skin disorders.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biomarkers / metabolism
  • Brazil / epidemiology
  • Female
  • HLA Antigens / metabolism*
  • HLA-G Antigens
  • Histocompatibility Antigens Class I / metabolism*
  • Humans
  • Immunohistochemistry
  • Male
  • Middle Aged
  • Prognosis
  • Scleroderma, Systemic / complications
  • Scleroderma, Systemic / metabolism*
  • Scleroderma, Systemic / mortality
  • Scleroderma, Systemic / pathology
  • Skin / blood supply
  • Skin / metabolism*
  • Skin / pathology
  • Skin Ulcer / etiology
  • Skin Ulcer / metabolism
  • Skin Ulcer / pathology
  • Survival Rate
  • Telangiectasis / etiology
  • Telangiectasis / metabolism
  • Telangiectasis / pathology

Substances

  • Biomarkers
  • HLA Antigens
  • HLA-G Antigens
  • Histocompatibility Antigens Class I