HLA-B27-derived peptides as autoantigens for T lymphocytes in ankylosing spondylitis

Arthritis Rheum. 1997 Nov;40(11):2047-54. doi: 10.1002/art.1780401118.

Abstract

Objective: To study whether peptides derived from the HLA-B27 molecule sequence can stimulate peripheral blood T lymphocytes (PBL) from patients with HLA-B27-associated spondylarthropathies.

Methods: PBL from 55 HLA-B27+ patients with ankylosing spondylitis (AS), 28 HLA-B27+ patients with other spondylarthropathies, 7 rheumatoid arthritis patients, and 30 HLA-B27+ and 22 HLA-B27- healthy controls were tested in lymphocyte proliferation assays with 4 synthetic peptides derived from the HLA-B*2705 molecule.

Results: A 13-mer peptide (B27PA) induced significant proliferative responses in 17 of the 55 AS patients (stimulation index [SI] 2.5-17.5), as well as in 3 of the HLA-B27+ healthy controls (SI 2.5-9.8). Another 13-mer peptide (B27PC) induced PBL proliferation (SI 2.7-5.5) in 10 AS patients and in some donors of the control groups. In B27PA-specific T cell lines, an expansion of cells positive for the gamma/delta T cell receptor could be demonstrated.

Conclusion: These results indicate that HLA-B27-derived peptides can be recognized as autoantigens by PBL of HLA-B27+ AS patients and B27+ healthy controls. Recent infections preceding the manifestation of AS may be involved in this process of anti-self major histocompatibility complex reactivity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Autoantigens / immunology*
  • Cell Line
  • Enzyme-Linked Immunosorbent Assay / methods
  • Female
  • Flow Cytometry
  • HLA-B27 Antigen / analysis*
  • HLA-B27 Antigen / chemistry
  • Humans
  • Interferon-gamma / metabolism
  • Lymphocyte Activation / drug effects
  • Male
  • Middle Aged
  • Peptides / pharmacology
  • Phenotype
  • Receptors, Antigen, T-Cell, gamma-delta / genetics
  • Spondylitis, Ankylosing / blood
  • Spondylitis, Ankylosing / immunology*
  • T-Lymphocytes / immunology*
  • T-Lymphocytes / metabolism

Substances

  • Autoantigens
  • HLA-B27 Antigen
  • Peptides
  • Receptors, Antigen, T-Cell, gamma-delta
  • Interferon-gamma