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New immunosuppressants: mycophenolate mofetil and 15-deoxyspergualin

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Disease-modifying Therapy in Vasculitides

Part of the book series: Progress in Inflammation Research ((PIR))

Abstract

Primary or idiopathic vasculitic syndromes are a group of inflammatory disorders of presumed autoimmune origin characterized by inflammation of blood vessels leading to vessel wall necrosis and (partial) obliteration or thrombosis of the vascular lumen. Clinical signs and symptoms are caused by disruption of adequate macro-and microcirculatory blood flow of organs or tissues by the vascular inflammatory proces. The classification of these idiopathic systemic vasculitic syndromes is based on the size and localization of the vessels predominantly involved and certain characteristics of the histopathology of the inflammatory process [1]. Several different classification schemes have been proposed, the latest modification being the scheme set up by a Consensus Conference in Chapel Hill in 1992 (Tab. 1) [2]. The factors involved in the pathogenesis of primary vasculitides are as yet unidentified. The possible autoimmune origin of these diseases is supported by the strong association of the presence of autoantibodies directed against neutrophil cytoplasmic antigens, so-called anti-neutrophil cytoplasmic antibodies (ANCA), in some of the primary small vessel vasculitides [2, 3].

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Stegeman, C.A., Birck, R. (2001). New immunosuppressants: mycophenolate mofetil and 15-deoxyspergualin. In: Kallenberg, C.G.M., Tervaert, J.W.C. (eds) Disease-modifying Therapy in Vasculitides. Progress in Inflammation Research. Birkhäuser, Basel. https://doi.org/10.1007/978-3-0348-8235-4_7

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  • DOI: https://doi.org/10.1007/978-3-0348-8235-4_7

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