Complement activation in ANCA-associated vasculitis

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Anca-associated Vasculitis and Complement System Activation

Small vessel vasculitides associated with anti-neutrophil cytoplasmic autoantibodies (ANCA) are severe systemic diseases that may affect any organ. Increasing clinical and experimental evidence indicates that ANCA are causally involved in disease pathogenesis mainly through activation of neutrophils resulting in endothelial cell injury. Recent studies suggest a previously unsuspected but crucia...

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Antineutrophil cytoplasm antibody (ANCA)-associated vasculitides are small-vessel vasculitides that include granulomatosis with polyangiitis (formerly Wegener's granulomatosis), microscopic polyangiitis, and eosinophilic granulomatosis with polyangiitis (Churg-Strauss syndrome). Renal-limited ANCA-associated vasculitides can be considered the fourth entity. Despite their rarity and still unknow...

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Antineutrophil cytoplasmic antibodies (ANCA)-associated vasculitis is the most common primary systemic small-vessel vasculitis to occur in adults. Although the etiology is not always known, the incidence of vasculitis is increasing, and the diagnosis and management of patients may be challenging because of its relative infrequency, changing nomenclature, and variability of clinical expression. ...

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ژورنال

عنوان ژورنال: Clinical pharmacology and therapy

سال: 2020

ISSN: 0869-5490

DOI: 10.32756/0869-5490-2020-3-55-60