4.7 Article

Interleukin 22 serum levels are associated with radiographic progression in rheumatoid arthritis

Journal

ANNALS OF THE RHEUMATIC DISEASES
Volume 70, Issue 8, Pages 1453-1457

Publisher

BMJ PUBLISHING GROUP
DOI: 10.1136/ard.2011.152074

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Funding

  1. Deutsche Forschungsgemeinschaft [SK59/4-1, Schu 786/2-5, Sonderforschungsbereich 571, D9]
  2. Graduiertenkolleg [1202, E2]
  3. medical faculty of LMU Munich

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Objectives To study the role of interleukin 22 (IL-22) in rheumatoid arthritis (RA). Methods IL-22 serum levels were measured in patients with early, treatment-naive RA (n=49) and in 45 age-and sex-matched healthy individuals as controls. Patients were assessed clinically and radiographically at baseline and followed up for 2 years. Correlations of IL-22 serum levels were sought with parameters of disease activity, serological markers, demographic factors and the incidence of erosions. IL-22 production by peripheral blood T cells was investigated by intracellular fl ow cytometry. Results 24 of 49 patients with RA demonstrated elevated IL-22 levels compared with the range of healthy controls. At baseline, a high percentage of these patients (8/ 24, 33%) demonstrated bone erosions, whereas only one patient (4%) from the group with normal IL-22 had erosions. During the 2 years of follow-up, six additional patients with increased IL-22 at baseline developed erosions. In contrast, none of the patients in whom IL-22 levels were normal developed erosions despite similar treatment regimens. Multivariate regression analysis accounting for other parameters predictive for erosions, such as the presence of rheumatoid factor or anti-cyclic citrullinated peptide antibodies and disease activity, showed that elevated IL-22 baseline levels were independently and signifi cantly associated with erosive RA. Cellular analysis demonstrated enhanced expression of IL-22 from CD4 T cells in RA. Conclusion IL-22 is elevated in the serum of half of the patients with RA. Elevated serum IL-22 allows discrimination between patients with different radiographic progression and indicates a possible involvement of IL-22 in the pathophysiology of RA.

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