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Cytokine and autoantibody profiling related to histopathological features in primary Sjögren's syndrome

Objective. To investigate a potential correlation between circulating cytokine and autoantibody levels and histopathological features in subgroups of patients with primary SS (pSS). Methods. Minor salivary gland biopsies from a cohort of 141 patients fulfilling the American–European consensus classi...

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Published in:Rheumatology (Oxford, England) England), 2009-09, Vol.48 (9), p.1102-1106
Main Authors: Reksten, Tove R., Jonsson, Malin V., Szyszko, Ewa A., Brun, Johan G., Jonsson, Roland, Brokstad, Karl A.
Format: Article
Language:English
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Summary:Objective. To investigate a potential correlation between circulating cytokine and autoantibody levels and histopathological features in subgroups of patients with primary SS (pSS). Methods. Minor salivary gland biopsies from a cohort of 141 patients fulfilling the American–European consensus classification criteria for pSS were re-examined and grouped according to focus score (FS) and germinal centre (GC) status; serum samples were analysed for autoantibodies, chemokines and cytokines. Results. Of the 115 available biopsies, 18 (16%) lacked characteristic focal mononuclear cell infiltrates [FS < 1 (FS−)] but patients were positive for Ro/SSA and/or La/SSB. IL-17, IL-1RA, IL-15, macrophage inflammatory protein (MIP)-1α, MIP-1β, eotaxin, IFN-α and IL-4 levels were significantly increased in the 27 (23%) patients with ectopic GC formation (GC+) in the salivary glands compared with the GC− patients (n = 70). In addition, minor differences in cytokine levels were found when comparing age groups. Conclusion. Degenerative changes observed in the minor salivary glands of patients with pSS may represent ‘burned out’ inflammation. The elevated levels of IL-4 found in these patients may influence the reduced salivary flow observed in GC+ patients. Increased titres of Th17-associated cytokines, IL-17, IL-1β and the IL-23 subunit IL-12p40, may indicate a higher activity of these cells in GC+ patients. Differences in cytokine levels may be utilized when sub-grouping the SS patients into disease phases and may consequently have implications for treatment.
ISSN:1462-0324
1462-0332
DOI:10.1093/rheumatology/kep149