Interleukin 22 serum levels are associated with radiographic progression in rheumatoid arthritis
Interleukin 22 serum levels are associated with radiographic progression in rheumatoid arthritis
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DOI:
10.1136/ard.2011.152074
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发表时间:
2011-08-01
影响因子:
27.4
通讯作者:
Skapenko, Alla
中科院分区:
文献类型:
--
作者:
Leipe, Jan;Schramm, Markus A.;Skapenko, Alla
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.