Anti-Neutrophil Cytoplasmic Autoantibody-Associated Vasculitides
A special issue of Antibodies (ISSN 2073-4468).
Deadline for manuscript submissions: closed (31 January 2019) | Viewed by 382
Special Issue Editor
Interests: glomerular disease; IgA nephropathy; ANCA vasculitis and glomerulonephritis; membranous nephropathy; lupus nephritis; complement-mediated glomerular diseases
Special Issues, Collections and Topics in MDPI journals
Special Issue Information
Dear Colleagues,
Anti-neutrophil cytoplasmic autoantibodies (ANCA)-associated vasculitides are characterized by the presence of ANCA in the circulation and a paucity of staining for immunoglobulins by histopathology. Genetic distinctions and discrete clinical syndromes or disease profiles have been associated with the type of ANCA. ANCA-associated vasculitides may occur as a renal-limited disease or as a component of systemic necrotizing small-vessel vasculitis. ANCA glomerulonephritis is the most common cause of crescentic glomerulonephritis, which often follows a course of rapid progression to end stage renal disease if left untreated. Speed in diagnosis of ANCA-associated vasculitis is the most crucial matter for these patients. Aggressive immunosuppressive therapy is justified by poor patient and renal survival rates in untreated patients. However, toxicity related to therapy is still remarkable and thus, continuing efforts are aiming to improve treatment options in order to minimize it.
This Special Issue intends to provide the reader with a comprehensive overview of the current insights into the pathogenesis and management of ANCA-associated vasculitides, focusing on important evidence-based developments in this critical field.
Dr. Sophia Lionaki
Guest Editor
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Keywords
- Epidemiology
- Pathogenesis
- The role of ANCA in pathogenesis
- Initial immunosuppressive therapy
- Maintenance therapy
- Management of persistent, refractory, or relapsing disease
- Prognosis; Predictors of patient and renal Survival
- Renal replacement modalities
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