Retinal S-antigen Th1 cell epitope mapping in patients with Behcet's disease

Graefes Arch Clin Exp Ophthalmol. 2009 Apr;247(4):555-60. doi: 10.1007/s00417-008-0970-9. Epub 2008 Oct 29.

Abstract

Background: Retinal S-antigen (S-Ag) is a most characterized autoantigen of autoimmune uveitis. The recognized immunodominant epitope of human S-Ag in patients with uveitis has not been identified. In this study, we selected certain patients with active uveitis to map the Th1 cell epitope spectrum of human S-Ag in Behcet's disease(BD).

Methods: Blood samples were taken from eight active BD patients who showed an immune response to 40 mixed overlapping peptides spanning the entire sequence of human S-Ag. Peripheral blood mononuclear cells were isolated and stimulated with single S-Ag peptide at 5 microg/ml or 20 microg/ml. Single-cell immune responses were measured by IFN-gamma ELIspot assay.

Results: BD patients heterogeneously responded to the S-Ag peptides at two concentrations. In general, the responses to 5 microg/ml peptides were slightly stronger than those to 20 microg/ml peptides, while the maximum SFC frequency to single peptide at the two concentrations was similar. Several peptides including P31, P35 and P40 induced a prominent response, with the frequency of S-Ag specific cells being about 0.007%. Significant reactivity pattern shift was noted in patients with different disease courses.

Conclusions: Certain active BD patients have S-Ag specific Th1 cells with a low frequency. The S-Ag epitope specificity between patients is highly heterogeneous, and varies with the uveitis course.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Amino Acid Sequence
  • Arrestin / immunology*
  • Autoantigens / immunology*
  • Behcet Syndrome / immunology*
  • Enzyme-Linked Immunosorbent Assay
  • Epitope Mapping
  • Humans
  • Immunity, Cellular
  • Immunodominant Epitopes / immunology*
  • Male
  • Molecular Sequence Data
  • Peptide Fragments / immunology
  • Th1 Cells / immunology*

Substances

  • Arrestin
  • Autoantigens
  • Immunodominant Epitopes
  • Peptide Fragments