GITRL is associated with increased autoantibody production in patients with rheumatoid arthritis

Clin Rheumatol. 2016 Sep;35(9):2195-202. doi: 10.1007/s10067-016-3280-3. Epub 2016 Apr 21.

Abstract

The study aimed to determine the serum level of glucocorticoid-induced tumor necrosis factor receptor family-related protein ligand (GITRL) in patients with rheumatoid arthritis (RA) and investigate its clinical significance. GITRL levels were measured by enzyme-linked immunosorbent assay (ELISA) in 88 RA patients, 20 osteoarthritis (OA) patients, and 20 healthy controls (HCs). Anti-cyclic citrullinated peptide (anti-CCP) antibodies and rheumatoid factor immunoglobulin G (RF-IgG) were also tested by ELISA. RF-IgM, anti-keratin antibody (AKA), and anti-perinuclear factor (APF) antibodies and the erythrocyte sedimentation rate (ESR), C-reactive protein (CRP), and immunoglobulins were measured by standard laboratory techniques. The disease activity was evaluated by the 28-joint count Disease Activity Score (DAS28). GITRL concentrations were significantly elevated in both serum and synovial fluid (SF) of RA patients. GITRL levels in RA sera were significantly higher than those in matched SFs. Positive correlations were found between serum GITRL levels and inflammation parameters or autoantibody production. GITRL levels are significantly elevated in RA serum and SF and are positively correlated with autoantibody production in RA, suggesting a role of GITRL in the development of RA.

Keywords: Autoantibody; Autoimmune disease; GITRL; Rheumatoid arthritis.

MeSH terms

  • Aged
  • Arthritis, Rheumatoid / blood*
  • Arthritis, Rheumatoid / immunology
  • Autoantibodies / blood*
  • C-Reactive Protein / metabolism
  • Female
  • Humans
  • Keratins / immunology
  • Male
  • Middle Aged
  • Osteoarthritis / blood
  • Osteoarthritis / immunology
  • Peptides, Cyclic / immunology
  • Synovial Fluid / metabolism
  • Tumor Necrosis Factors / blood*

Substances

  • Autoantibodies
  • Peptides, Cyclic
  • TNFSF18 protein, human
  • Tumor Necrosis Factors
  • cyclic citrullinated peptide
  • Keratins
  • C-Reactive Protein