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Ann Rheum Dis. 2011 Aug;70(8):1453-7. doi: 10.1136/ard.2011.152074. Epub 2011 May 18.

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

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1
Division of Rheumatology, Medizinische Poliklinik, University of Munich, Munich, Germany.

Abstract

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 flow 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 significantly 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.

PMID:
21593004
DOI:
10.1136/ard.2011.152074
[Indexed for MEDLINE]
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