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Simultaneous Automated Screening and Confirmatory Testing for Vasculitis-Specific ANCA
Anti-neutrophil cytoplasmic antibodies (ANCA) are the serological hallmark of small vessel vasculitis, so called ANCA-associated vasculitis. The international consensus requires testing by indirect immunofluorescence (IIF) on human ethanol-fixed neutrophils (ethN) as screening followed by confirmati...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4166465/ https://www.ncbi.nlm.nih.gov/pubmed/25225805 http://dx.doi.org/10.1371/journal.pone.0107743 |
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author | Sowa, Mandy Grossmann, Kai Knütter, Ilka Hiemann, Rico Röber, Nadja Anderer, Ursula Csernok, Elena Bogdanos, Dimitrios P. Borghi, Maria Orietta Meroni, Pier Luigi Schierack, Peter Reinhold, Dirk Conrad, Karsten Roggenbuck, Dirk |
author_facet | Sowa, Mandy Grossmann, Kai Knütter, Ilka Hiemann, Rico Röber, Nadja Anderer, Ursula Csernok, Elena Bogdanos, Dimitrios P. Borghi, Maria Orietta Meroni, Pier Luigi Schierack, Peter Reinhold, Dirk Conrad, Karsten Roggenbuck, Dirk |
author_sort | Sowa, Mandy |
collection | PubMed |
description | Anti-neutrophil cytoplasmic antibodies (ANCA) are the serological hallmark of small vessel vasculitis, so called ANCA-associated vasculitis. The international consensus requires testing by indirect immunofluorescence (IIF) on human ethanol-fixed neutrophils (ethN) as screening followed by confirmation with enzyme-linked immunosorbent assays (ELISAs). This study evaluates the combination of cell- and microbead-based digital IIF analysis of ANCA in one reaction environment by the novel multiplexing CytoBead technology for simultaneous screening and confirmatory ANCA testing. Sera of 592 individuals including 118 patients with ANCA-associated vasculitis, 133 with rheumatoid arthritis, 49 with infectious diseases, 77 with inflammatory bowel syndrome, 20 with autoimmune liver diseases, 70 with primary sclerosing cholangitis and 125 blood donors were tested for cytoplasmic ANCA (C-ANCA) and perinuclear ANCA (P-ANCA) by classical IIF and ANCA to proteinase 3 (PR3) and myeloperoxidase (MPO) by ELISA. These findings were compared to respective ANCA results determined by automated multiplex CytoBead technology using ethN and antigen-coated microbeads for microbead immunoassays. There was a good agreement for PR3- and MPO-ANCA and a very good one for P-ANCA and C-ANCA by classical and multiplex analysis (Cohen's kappa [κ] = 0.775, 0.720, 0.876, 0.820, respectively). The differences between classical testing and CytoBead analysis were not significant for PR3-ANCA, P-ANCA, and C-ANCA (p<0.05, respectively). The prevalence of confirmed positive ANCA findings by classical testing (IIF and ELISA) compared with multiplex CytoBead analysis (IIF and microbead immunoassay positive) resulted in a very good agreement (κ = 0.831) with no significant difference of both methods (p = 0.735). Automated endpoint-ANCA titer detection in one dilution demonstrated a very good agreement with classical analysis requiring dilution of samples (κ = 0.985). Multiplexing by CytoBead technology can be employed for simultaneous screening and quantitative confirmation of ANCA. This novel technique provides fast and cost-effective ANCA analysis by automated digital IIF for the first time. |
format | Online Article Text |
id | pubmed-4166465 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-41664652014-09-22 Simultaneous Automated Screening and Confirmatory Testing for Vasculitis-Specific ANCA Sowa, Mandy Grossmann, Kai Knütter, Ilka Hiemann, Rico Röber, Nadja Anderer, Ursula Csernok, Elena Bogdanos, Dimitrios P. Borghi, Maria Orietta Meroni, Pier Luigi Schierack, Peter Reinhold, Dirk Conrad, Karsten Roggenbuck, Dirk PLoS One Research Article Anti-neutrophil cytoplasmic antibodies (ANCA) are the serological hallmark of small vessel vasculitis, so called ANCA-associated vasculitis. The international consensus requires testing by indirect immunofluorescence (IIF) on human ethanol-fixed neutrophils (ethN) as screening followed by confirmation with enzyme-linked immunosorbent assays (ELISAs). This study evaluates the combination of cell- and microbead-based digital IIF analysis of ANCA in one reaction environment by the novel multiplexing CytoBead technology for simultaneous screening and confirmatory ANCA testing. Sera of 592 individuals including 118 patients with ANCA-associated vasculitis, 133 with rheumatoid arthritis, 49 with infectious diseases, 77 with inflammatory bowel syndrome, 20 with autoimmune liver diseases, 70 with primary sclerosing cholangitis and 125 blood donors were tested for cytoplasmic ANCA (C-ANCA) and perinuclear ANCA (P-ANCA) by classical IIF and ANCA to proteinase 3 (PR3) and myeloperoxidase (MPO) by ELISA. These findings were compared to respective ANCA results determined by automated multiplex CytoBead technology using ethN and antigen-coated microbeads for microbead immunoassays. There was a good agreement for PR3- and MPO-ANCA and a very good one for P-ANCA and C-ANCA by classical and multiplex analysis (Cohen's kappa [κ] = 0.775, 0.720, 0.876, 0.820, respectively). The differences between classical testing and CytoBead analysis were not significant for PR3-ANCA, P-ANCA, and C-ANCA (p<0.05, respectively). The prevalence of confirmed positive ANCA findings by classical testing (IIF and ELISA) compared with multiplex CytoBead analysis (IIF and microbead immunoassay positive) resulted in a very good agreement (κ = 0.831) with no significant difference of both methods (p = 0.735). Automated endpoint-ANCA titer detection in one dilution demonstrated a very good agreement with classical analysis requiring dilution of samples (κ = 0.985). Multiplexing by CytoBead technology can be employed for simultaneous screening and quantitative confirmation of ANCA. This novel technique provides fast and cost-effective ANCA analysis by automated digital IIF for the first time. Public Library of Science 2014-09-16 /pmc/articles/PMC4166465/ /pubmed/25225805 http://dx.doi.org/10.1371/journal.pone.0107743 Text en © 2014 Sowa et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Sowa, Mandy Grossmann, Kai Knütter, Ilka Hiemann, Rico Röber, Nadja Anderer, Ursula Csernok, Elena Bogdanos, Dimitrios P. Borghi, Maria Orietta Meroni, Pier Luigi Schierack, Peter Reinhold, Dirk Conrad, Karsten Roggenbuck, Dirk Simultaneous Automated Screening and Confirmatory Testing for Vasculitis-Specific ANCA |
title | Simultaneous Automated Screening and Confirmatory Testing for Vasculitis-Specific ANCA |
title_full | Simultaneous Automated Screening and Confirmatory Testing for Vasculitis-Specific ANCA |
title_fullStr | Simultaneous Automated Screening and Confirmatory Testing for Vasculitis-Specific ANCA |
title_full_unstemmed | Simultaneous Automated Screening and Confirmatory Testing for Vasculitis-Specific ANCA |
title_short | Simultaneous Automated Screening and Confirmatory Testing for Vasculitis-Specific ANCA |
title_sort | simultaneous automated screening and confirmatory testing for vasculitis-specific anca |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4166465/ https://www.ncbi.nlm.nih.gov/pubmed/25225805 http://dx.doi.org/10.1371/journal.pone.0107743 |
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