Search engine for discovering works of Art, research articles, and books related to Art and Culture
ShareThis
Javascript must be enabled to continue!

Value of a New Automated Fluorescence Immunoassay (EliA) for PR3 and MPO‐ANCA in Monitoring Disease Activity in ANCA‐Associated Systemic Vasculitis

View through CrossRef
A bstract : The value of anti‐neutrophil cytoplasmic antibody (ANCA) detection for monitoring disease activity in ANCA‐associated systemic vasculitis (AASV) remains controversial. The aim of our work was to rate the performance of a new automated fluorescence PR3 and MPO‐ANCA immunoassay (EliA) for monitoring disease activity in AASV. We evaluated 100 serum samples from 71 AASV patients (with Wegener's granulomatosis, microscopic polyangiitis, and Churg‐Strauss syndrome) as well as sera from 58 pathological and 35 normal controls. In addition to PR3 and MPO‐ANCA EliA, we performed indirect immunofluorescence and “homemade” PR3 and MPO‐ANCA ELISA tests. In AASV patients, ANCA levels were correlated with disease activity, according to the Birmingham Vasculitis Activity Score (BVAS). We derived cutoff limits from receiver operating characteristic (ROC) curve analysis comparing AASV with pathological controls. Our results showed that EliA and ELISA had comparable sensitivity (76%) and specificity (95%). The analysis of active versus inactive status and correlation with ANCA levels showed a clear difference between BVAS Group I (score ≤ 4) and BVAS Group II (scores > 4) (AUC = 0.86 vs. 0.72; relative risk [RR] = 2.4; P < 0.0001 ) for PR3‐ANCA, but not for MPO‐ANCA (AUC = 0.94 vs. 0.87; RR = 1.48; P = 0 .46). Serial serum samples from 16 patients were examined in detail. For the majority of patients, for both PR3 and MPO‐ANCA, change in titer was strongly associated with change in BVAS score. Our data showed a good correlation between ANCA titer (especially for PR3) and AASV disease activity. We recommend that ANCA titer be used to monitor AASV disease activity with the caveat that a few exceptions, in particular with MPO‐ANCA, are possible.
Title: Value of a New Automated Fluorescence Immunoassay (EliA) for PR3 and MPO‐ANCA in Monitoring Disease Activity in ANCA‐Associated Systemic Vasculitis
Description:
A bstract : The value of anti‐neutrophil cytoplasmic antibody (ANCA) detection for monitoring disease activity in ANCA‐associated systemic vasculitis (AASV) remains controversial.
The aim of our work was to rate the performance of a new automated fluorescence PR3 and MPO‐ANCA immunoassay (EliA) for monitoring disease activity in AASV.
We evaluated 100 serum samples from 71 AASV patients (with Wegener's granulomatosis, microscopic polyangiitis, and Churg‐Strauss syndrome) as well as sera from 58 pathological and 35 normal controls.
In addition to PR3 and MPO‐ANCA EliA, we performed indirect immunofluorescence and “homemade” PR3 and MPO‐ANCA ELISA tests.
In AASV patients, ANCA levels were correlated with disease activity, according to the Birmingham Vasculitis Activity Score (BVAS).
We derived cutoff limits from receiver operating characteristic (ROC) curve analysis comparing AASV with pathological controls.
Our results showed that EliA and ELISA had comparable sensitivity (76%) and specificity (95%).
The analysis of active versus inactive status and correlation with ANCA levels showed a clear difference between BVAS Group I (score ≤ 4) and BVAS Group II (scores > 4) (AUC = 0.
86 vs.
0.
72; relative risk [RR] = 2.
4; P < 0.
0001 ) for PR3‐ANCA, but not for MPO‐ANCA (AUC = 0.
94 vs.
0.
87; RR = 1.
48; P = 0 .
46).
Serial serum samples from 16 patients were examined in detail.
For the majority of patients, for both PR3 and MPO‐ANCA, change in titer was strongly associated with change in BVAS score.
Our data showed a good correlation between ANCA titer (especially for PR3) and AASV disease activity.
We recommend that ANCA titer be used to monitor AASV disease activity with the caveat that a few exceptions, in particular with MPO‐ANCA, are possible.

Related Results

Lessons from a double-transgenic neutrophil approach to induce antiproteinase 3 antibody–mediated vasculitis in mice
Lessons from a double-transgenic neutrophil approach to induce antiproteinase 3 antibody–mediated vasculitis in mice
Abstract ANCA to either PR3 or MPO are found in patients with necrotizing vasculitis and glomerulonephritis. ANCA binding to their target antigens on neutrophils and...
The plasma proteome reveals distinct signaling pathways associated with PR3-ANCA positive and MPO-ANCA positive vasculitis
The plasma proteome reveals distinct signaling pathways associated with PR3-ANCA positive and MPO-ANCA positive vasculitis
ObjectiveDespite recent advances, the pathophysiological mechanisms underlying anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitides (AAV) remain incompletely underst...
The Diagnostic and Clinical Utility of Autoantibodies in Systemic Vasculitis
The Diagnostic and Clinical Utility of Autoantibodies in Systemic Vasculitis
Considerable progress has been made in understanding the role of autoantibodies in systemic vasculitides (SV), and consequently testing for anti-neutrophil cytoplasmic antibodies (...
Myeloperoxidase (MPO) in Synovial Tissue and Serum in Patients with Psoriatic Arthritis and Osteoarthritis—A Pilot Study
Myeloperoxidase (MPO) in Synovial Tissue and Serum in Patients with Psoriatic Arthritis and Osteoarthritis—A Pilot Study
The aim of this study was to determine the serum level of myeloperoxidase (MPO) and level of synovial fluid MPO of patients with psoriatic arthritis (PsA); the presence of myeloper...
Abstract A053: Tumor-localized myeloperoxidase enhances tumor chemoresistance, migration, and invason.
Abstract A053: Tumor-localized myeloperoxidase enhances tumor chemoresistance, migration, and invason.
Abstract Neutrophils frequently infiltrate solid tumors, where they can have pro-tumor effects that significantly worsen clinical outcomes for many types of cancer. ...
Disrupting the CD177:proteinase 3 membrane complex reduces anti-PR3 antibody-induced neutrophil activation
Disrupting the CD177:proteinase 3 membrane complex reduces anti-PR3 antibody-induced neutrophil activation
ABSTRACT CD177 is a neutrophil-specific receptor presenting proteinase 3 (PR3) autoantigen on the neutrophil surface. CD177 expression is restric...

Back to Top