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Effects of TNF inhibitor on innate inflammatory and Th17 cytokines in stimulated whole blood from rheumatoid arthritis patients

Background Recent studies point to important roles for IL-17 and Th17 cells in sustaining chronic inflammation and articular destruction in rheumatoid arthritis (RA). We investigated the effects of TNF inhibitor on innate inflammatory and Th17 cytokines production by ex vivo lipopolysaccharide (LPS)...

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Published in:Inflammopharmacology 2012-12, Vol.20 (6), p.323-330
Main Authors: Zivojinovic, Sladjana, Pejnovic, Nada, Sefik-Bukilica, Mirjana, Kovacevic, Ljiljana, Soldatovic, Ivan, Bugarski, Diana, Mojsilovic, Slavko, Damjanov, Nemanja
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Language:English
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Summary:Background Recent studies point to important roles for IL-17 and Th17 cells in sustaining chronic inflammation and articular destruction in rheumatoid arthritis (RA). We investigated the effects of TNF inhibitor on innate inflammatory and Th17 cytokines production by ex vivo lipopolysaccharide (LPS)-stimulated whole blood in patients with RA and the associations of cytokine levels in whole blood cultures with autoantibodies and markers of disease activity. Materials and methods Whole blood cultures from 18 healthy volunteers and 19 RA patients on etanercept therapy were stimulated with LPS and the production of IL-6, TNF-α, IL-23, IL-17A and IL-21 was measured by ELISA. Results After stimulation with LPS, the interleukin (IL)-17A ( p  = 0.020) and IL-21 ( p  = 0.0001) secretions were significantly higher in patients with RA than in controls, while the TNF-α ( p  = 0.002) was significantly lower at baseline. Etanercept significantly decreased IL-21 production ( p  = 0.007), while IL-6 production ( p  = 0.005) significantly increased after 6 months of therapy. IL-21 significantly correlated with RF ( r  = 0.917, p  
ISSN:0925-4692
1568-5608
DOI:10.1007/s10787-012-0143-7