Disturbed expression of Fas/FasL on CD4(+) and CD8(+)T cells in Behcet's disease, Vogt-Koyanagi-Harada syndrome, and idiopathic anterior uveitis

Ocul Immunol Inflamm. 2001 Sep;9(3):185-91. doi: 10.1076/ocii.9.3.185.3961.

Abstract

Aims: To evaluate the expression of Fas/FasL antigen on peripheral blood T lymphocytes in patients with Behcet's disease, Vogt-Koyanagi-Harada (VKH) syndrome, and idiopathic anterior uveitis.

Methods: The expression of Fas and FasL on peripheral blood T lymphocytes was determined using flow cytometry in 26 patients with Behcet's disease (BD), 17 patients with VKH syndrome, 25 patients with idiopathic anterior uveitis, and 43 healthy individuals (controls).

Results: A higher proportion of CD4(+) T cells expressing Fas was noted in patients with Behcet's disease (25.70 +/- 7.32%), VKH syndrome (19.60 +/- 11.02%), and idiopathic anterior uveitis (20.81+/- 7.40%) compared with controls (14.02 +/- 6.30%). The expression of Fas on CD8(+) cells from patients with Behcet's disease (9.47 +/- 6.97%) and VKH syndrome (6.84+/- 5.5%) was also higher than that seen in controls (3.47+/- 2.75%). There was no difference in FasL expression on T cells between patients and controls except that a lower expression of FasL on CD8(+) T cells was noted in patients with idiopathic anterior uveitis.

Conclusion: A disturbed expression of Fas and FasL on T cells is present in patients with Behcet's disease, VKH syndrome, and idiopathic anterior uveitis, which may be involved in the perpetuation and recurrence of uveitis.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Behcet Syndrome / immunology*
  • CD4-Positive T-Lymphocytes / immunology*
  • CD8-Positive T-Lymphocytes / immunology*
  • Fas Ligand Protein
  • Female
  • Flow Cytometry
  • Fluorescent Antibody Technique, Indirect
  • Humans
  • Ligands
  • Male
  • Membrane Glycoproteins / metabolism*
  • Uveitis, Anterior / immunology*
  • Uveomeningoencephalitic Syndrome / immunology*
  • fas Receptor / metabolism*

Substances

  • FASLG protein, human
  • Fas Ligand Protein
  • Ligands
  • Membrane Glycoproteins
  • fas Receptor