Eotaxin-3 is involved in Churg-Strauss syndrome - A serum marker closely correlating with disease activity

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Abstract

Objective. Churg-Strauss Syndrome (CSS) is characterized by excessive eosinophil accumulation in peripheral blood and affected tissues with development of granulomatous vasculitic organ damage. The contribution of eosinophil-chemotactic cytokines (eotaxin family) to eosinophilia and disease activity in CSS is unknown. Thus, we compared serum levels of the eotaxin family members in CSS patients with healthy and disease controls. Methods. Forty patients with CSS diagnosed according to ACR 1990 criteria, 30 healthy controls (HC) and 57 disease controls (28 asthma, 20 small vessel vasculitis, 9 hypereosinophilic syndrome) were studied. Clinical data were collected and serum levels of eotaxin-1, -2 and -3 were determined by ELISA. Further, immunohistochemistry was applied to identify eotaxin-3 expression in tissue biopsies from patients with CSS. Results. In contrast to eotaxin-1 and -2, eotaxin-3 was highly elevatedin serum samples of active CSS patients and correlated highly significantly with eosinophil counts, total immunoglobulin E (IgE) levels and acute-phase parameters. Moreover, eotaxin-3 was not elevated in other eosinophilic and vasculitic diseases. Immunohistochemical analysis revealed strong expression of eotaxin-3 in endothelial and inflammatory cells in affected tissues of active CSS patients. Conclusions. This study reveals the specific association of elevated eotaxin-3 expression with high disease activity and eosinophilia in CSS patients. Eotaxin-3 might thus be a pathogenic player, biomarker and potential therapeutic target in CSS. © The Author 2008. Published by Oxford University Press on behalf of the British Society for Rheumatology. All rights reserved.

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Polzer, K., Karonitsch, T., Neumann, T., Eger, G., Haberler, C., Soleiman, A., … Zwerina, J. (2008). Eotaxin-3 is involved in Churg-Strauss syndrome - A serum marker closely correlating with disease activity. Rheumatology, 47(6), 804–808. https://doi.org/10.1093/rheumatology/ken033

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