Results 11 to 20 of about 8,073,410 (232)

Immunopathogenesis of ANCA-Associated Vasculitis [PDF]

open access: yesInternational Journal of Molecular Sciences, 2020
Anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis is an autoimmune disorder which affects small- and, to a lesser degree, medium-sized vessels. ANCA-associated vasculitis encompasses three disease phenotypes: granulomatosis with polyangiitis (GPA), microscopic polyangiitis (MPA), and eosinophilic granulomatosis with polyangiitis (EGPA).
Andreas Kronbichler   +32 more
core   +14 more sources

Pathogenesis of ANCA-associated Vasculitis [PDF]

open access: yesRheumatic Disease Clinics of North America, 2010
Antineutrophil cytoplasm antibody (ANCA)-associated vasculitis (AAV) comprises a group of systemic inflammatory vasculitides associated with circulating autoantibodies directed against the neutrophil granule components proteinase 3 and myeloperoxidase.
Julia, Flint   +2 more
openaire   +3 more sources

ANCA associated vasculitis subtypes: Response (response to letter) [PDF]

open access: yes, 2022
Many thanks for the opportunity to respond to the interesting letter to the Editor from Merkel, Jayne, and Bekker, with regard to our publication “ANCA Associated Vasculitis Subtypes: Recent Insights and Future Perspectives”.1In the management section of
Robson, Joanna C   +6 more
core   +1 more source

Autoantibodies Against Lysosome Associated Membrane Protein-2 (LAMP-2) in Pediatric Chronic Primary Systemic Vasculitis

open access: yesFrontiers in Immunology, 2021
BackgroundAnti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) is a small vessel vasculitis in adults and children that commonly affects the kidneys.
Kristen M. Gibson   +9 more
doaj   +1 more source

Prevalence and clinical association of the presence of anti-neutrophilic cytoplasmic antibody in systemic sclerosis

open access: yesArchives of Medical Science, 2020
Introduction Anti-neutrophilic cytoplasmic antibody (ANCA) has been reported in systemic sclerosis (SSc). Some clinical features of SSc can also be presented with ANCA-associated vasculitis.
Ajanee Mahakkanukrauh   +3 more
doaj   +1 more source

ANCA-associated vasculitis overlaps with systemic sclerosis: a case report and literature review

open access: yesEuropean Journal of Medical Research, 2021
Background Systemic sclerosis (SSc) and anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) both affect the kidney and may cause renal failure. Treatment of AAV is dramatically different from that of SSc renal crisis (SRC).
Rui Wu, Jiang Su, Yu-rong Zou, Jing Zhu
doaj   +1 more source

ANCA-associated renal vasculitis [PDF]

open access: yesKidney International, 2002
To the Editor: The Nephrology Forum discussed by Professor Savage reminded us of two items about ANCA-associated renal vasculitis (AARV): (1) the complex pathogenesis, where ANCA are much but not enough; and (2) the role of cytokines1.
Campo A, Grill A, STRATTA, Piero
openaire   +2 more sources

The Diagnostic and Clinical Utility of Autoantibodies in Systemic Vasculitis

open access: yesAntibodies, 2019
Considerable progress has been made in understanding the role of autoantibodies in systemic vasculitides (SV), and consequently testing for anti-neutrophil cytoplasmic antibodies (ANCA), anti-glomerular basement membrane antibodies (anti-GBM), and anti ...
Elena Csernok
doaj   +1 more source

Checkpoint inhibitor-related renal vasculitis and use of rituximab

open access: yesJournal for ImmunoTherapy of Cancer, 2020
The percentage of patients with cancer eligible for checkpoint inhibitor (CPI) therapy has increased rapidly over the past few years and approaches 45%.
Noha Abdel-Wahab   +6 more
doaj   +1 more source

ANCA Associated Vasculitis Treated with Ultra-low Dose Rituximab: A Case Report

open access: yesXiehe Yixue Zazhi, 2023
We reported a case of ANCA-associated vasculitis with pulmonary and renal involvement that was effectively treated with glucocorticoids, cyclophosphamide, and plasma exchange therapy.
WU Haiting, LI Hang
doaj   +1 more source

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