4.5 Article

C Nuclear Factor-κB-inducing Kinase Is Expressed in Synovial Endothelial Cells in Patients with Early Arthritis and Correlates with Markers of Inflammation: A Prospective Cohort Study

Journal

JOURNAL OF RHEUMATOLOGY
Volume 42, Issue 9, Pages 1573-1581

Publisher

J RHEUMATOL PUBL CO
DOI: 10.3899/jrheum.150245

Keywords

NUCLEAR FACTOR-kappa B; NF-kappa B-INDUCING KINASE; RHEUMATOID ARTHRITIS; SYNOVIUM; EARLY ARTHRITIS

Categories

Funding

  1. Dutch Arthritis Foundation [06-1-303, 11-1-407, 12-2-050]
  2. Netherlands Organization for Health Research and Development (ZonMw) [200310003]
  3. Netherlands Organization for Scientific Research (NHW) [91696015]
  4. Clinical Fellowship (ZonMw) [90700359]
  5. Innovative Medicines Initiative European Union [115142]
  6. European Union Seventh Framework Programme (EuroTEAM) [FP7-HEALTHF2-2012, 305549]

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Objective. The nuclear factor-kappa B (NF-kappa B) family of transcription factors is strongly involved in synovial inflammation. We have previously shown that NF-kappa B-inducing kinase (NIK) is a key regulator of inflammation-induced angiogenesis in rheumatoid arthritis (RA) synovial tissue (ST). Here, we investigated synovial NIK expression in patients with early arthritis and in autoantibody-positive individuals at risk of developing RA. Methods. ST biopsies were obtained by arthroscopy from 154 patients with early arthritis (duration < 1 yr) with various diagnoses and 54 IgM rheumatoid factor-positive and/or anticitrullinated protein antibodies-positive individuals without evidence of arthritis. ST was stained for NIK and endothelial cell (EC) markers. Additionally, measures of disease activity were collected and contrast-enhanced magnetic resonance imaging (MRI) was performed in a subset of these patients. Results. In patients with early arthritis, NIK was predominantly expressed in EC of small blood vessels. Further, NIK expression correlated with erythrocyte sedimentation rate (r 0.184, p = 0.024), C-reactive protein (r 0.194, p = 0.017), joint swelling (r 0.297, p < 0.001), synovial immune cell markers (lining r 0.585, p < 0.001; sublining macrophages r 0.728, p < 0.001; T cells r 0.733, p < 0.001; and B cells r 0.264, p = 0.040), MRI effusion (r 0.665, p < 0.001), MRI synovitis (r 0.632, p < 0.001), and MRI total score (r 0.569, p < 0.001). In 18.5% of autoantibody-positive individuals, ST NIK+EC were present, but this was not predictive of the development of arthritis. Conclusion. NIK+EC are present in the earliest phase of synovial inflammation and may be indicative of high angiogenic activity in the inflamed ST. Therefore, NIK+EC may play an important role in the persistence of synovitis. Collectively, our data underscore the importance of angiogenesis in synovial inflammation and identify NIK as a potential therapeutic target in arthritis.

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