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Other Biological Therapies in Primary Sjögren’s Syndrome

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Sjögren’s Syndrome

Abstract

Sjögren’s syndrome (SS) is a systemic autoimmune disease that mainly affects the exocrine glands and usually presents as persistent dryness of the mouth and eyes. SS typically affects white perimenopausal women, with an incidence of 4–5 cases per 100,000. At present, there is no treatment capable of modifying the evolution of SS and the therapeutic approach is based on symptomatic replacement or stimulation of glandular secretions, using substitutive and oral muscarinic agents. Extraglandular involvement requires organ-specific therapy generally based upon some combination of glucocorticoids and immunosuppressive agents, similar to that applied in patients with systemic lupus erythematosus (SLE) [1].

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Brito-Zerón, P., Diaz-Lagares, C., Soto-Cárdenas, M.J., Ramos-Casals, M., Khamashta, M.A. (2011). Other Biological Therapies in Primary Sjögren’s Syndrome. In: Ramos-Casals, M., Stone, J., Moutsopoulos, H. (eds) Sjögren’s Syndrome. Springer, London. https://doi.org/10.1007/978-0-85729-947-5_41

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  • DOI: https://doi.org/10.1007/978-0-85729-947-5_41

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