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Clinical features of patients with anti-neutrophil cytoplasmic autoantibodies targeting native myeloperoxidase antigen.

Authors :
Yamanishi, Yuji
Ito-Ihara, Toshiko
Nagao, Tomokazu
Uno, Kazuko
Kobayashi, Shigeto
Muso, Eri
Shane, Peter
Firestein, Gary
Hashimoto, Hiroshi
Okazaki, Tomio
Suzuki, Kazuo
Source :
Modern Rheumatology; Sep2013, Vol. 23 Issue 5, p963-971, 9p
Publication Year :
2013

Abstract

Objectives: Anti-neutrophil cytoplasmic autoantibodies (ANCA) are useful diagnostic markers in systemic vasculitic disorders with small-vessel involvement, but depending on the particular test used, the myeloperoxidase (MPO)-ANCA results are variable. In the present study, we performed a comparative analysis between our originally developed nMPO-ANCA assay that targets the native MPO antigen and other commercially available assays using sera of patients with clinical features of ANCA-associated vasculitis (AAV). Methods: Sera of 24 patients strongly suspected of having AAV were examined for the presence of MPO-ANCAs by our nMPO-ANCA assay and by other commercial-based MPO-ANCA assays. These results were correlated to indirect immunofluorescence microscopy staining patterns and patient clinical parameters. Results: Eighteen out of 24 patients (75 %) were positive for nMPO-ANCA, compared with 13 out of 24 patients (54 %) by one of the most frequently used commercial-based MPO-ANCA enzyme-linked immunosorbent assays (ELISAs) in Japan. Interestingly, the patients who tested positive with our nMPO-ANCA assay alone showed clinical features of AAV marked by continuous fever, polyarthritis, and mild nephritis. The titers of nMPO-ANCA decreased in association with clinical improvement after treatment. Conclusions: Our data suggest that a positive nMPO-ANCA result, which identifies antibodies to human native MPO antigen, correlates with AAV disease activity. Moreover, the nMPO-ANCA test has clinical utility in detecting AAV-affected patients who have tested negative using commercially available assays. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14397595
Volume :
23
Issue :
5
Database :
Complementary Index
Journal :
Modern Rheumatology
Publication Type :
Academic Journal
Accession number :
90309690
Full Text :
https://doi.org/10.3109/s10165-012-0781-z