Interleukin-20 is triggered by TLR ligands and associates with disease activity in patients with rheumatoid arthritis
Language English Country Great Britain, England Media print-electronic
Document type Journal Article
PubMed
28662439
DOI
10.1016/j.cyto.2017.06.009
PII: S1043-4666(17)30166-7
Knihovny.cz E-resources
- Keywords
- Disease activity, Inflammation, Interleukin-20, Rheumatoid arthritis,
- MeSH
- Adult MeSH
- Immunohistochemistry MeSH
- Interleukins blood metabolism MeSH
- Leukocytes, Mononuclear drug effects immunology MeSH
- Middle Aged MeSH
- Humans MeSH
- Ligands MeSH
- Lipopolysaccharides immunology MeSH
- Arthritis, Rheumatoid blood immunology physiopathology MeSH
- Aged MeSH
- Synovial Fluid immunology MeSH
- Toll-Like Receptors immunology MeSH
- Inflammation MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- interleukin 20 MeSH Browser
- Interleukins MeSH
- Ligands MeSH
- Lipopolysaccharides MeSH
- Toll-Like Receptors MeSH
BACKGROUND: Interleukin (IL)-20 is a pro-inflammatory cytokine that may be implicated in the pathogenesis of rheumatoid arthritis (RA). This study aimed to determine the association between IL-20 and disease activity in patients with RA. METHODS: The levels of serum and synovial fluid IL-20 were measured in patients with RA and OA. The disease activity was assessed based on the Disease Activity Score of 28 joints (DAS28). The expression of IL-20 in synovial tissue samples from patients with RA and OA were determined by immunohistochemistry. Immunofluorescence staining was used to co-localize IL-20 with selected cells. The secretion of IL-20 was analysed in human peripheral blood mononuclear cells (PBMCs) of patients with RA. RESULTS: Synovial fluid and synovial tissue IL-20 were significantly increased in patients with RA compared with patients with OA. The expression of IL-20 in RA synovial tissue was particularly associated with macrophages and neutrophil granulocytes, but also with synovial fibroblasts and lymphocytes. The IL-20 levels in synovial fluid correlated with DAS28 (r=0.434; p=0.015) and were significantly elevated in anti-CCP positive RA compared with anti-CCP negative RA (122.3±104.1pg/ml and 45.9±35.8pg/ml; p=0.008). IL-20 production from PBMCs was induced by Poly I:C and LPS but not with pro-inflammatory cytokines, such as TNF-α or IL-1. CONCLUSION: Our data showed that IL-20 is independently associated with RA disease activity and may be triggered by TLR ligands at local sites of inflammation.
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