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Evaluation of Clinical Interest of Anti-Aquaporin-4 Autoantibody Followup in Neuromyelitis Optica

Neuromyelitis optica (NMO) is an autoimmune disease in which a specific biomarker named NMO-IgG and directed against aquaporin-4 (AQP4) has been found. A correlation between disease activity and anti-AQP4 antibody (Ab) serum concentration or complement-mediated cytotoxicity has been reported, but th...

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Autores principales: Chanson, Jean-Baptiste, Alame, Melissa, Collongues, Nicolas, Blanc, Frédéric, Fleury, Marie, Rudolf, Gabrielle, de Seze, Jérôme, Vincent, Thierry
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3655457/
https://www.ncbi.nlm.nih.gov/pubmed/23710199
http://dx.doi.org/10.1155/2013/146219
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author Chanson, Jean-Baptiste
Alame, Melissa
Collongues, Nicolas
Blanc, Frédéric
Fleury, Marie
Rudolf, Gabrielle
de Seze, Jérôme
Vincent, Thierry
author_facet Chanson, Jean-Baptiste
Alame, Melissa
Collongues, Nicolas
Blanc, Frédéric
Fleury, Marie
Rudolf, Gabrielle
de Seze, Jérôme
Vincent, Thierry
author_sort Chanson, Jean-Baptiste
collection PubMed
description Neuromyelitis optica (NMO) is an autoimmune disease in which a specific biomarker named NMO-IgG and directed against aquaporin-4 (AQP4) has been found. A correlation between disease activity and anti-AQP4 antibody (Ab) serum concentration or complement-mediated cytotoxicity has been reported, but the usefulness of longitudinal evaluation of these parameters remains to be evaluated in actual clinical practice. Thirty serum samples from 10 NMO patients positive for NMO-IgG were collected from 2006 to 2011. Anti-AQP4 Ab serum concentration and complement-mediated cytotoxicity were measured by flow cytometry using two quantitative cell-based assays (CBA) and compared with clinical parameters. We found a strong correlation between serum anti-AQP4 Ab concentration and complement-mediated cytotoxicity (P < 0.0001). Nevertheless, neither relapse nor worsening of impairment level was closely associated with a significant increase in serum Ab concentration or cytotoxicity. These results suggest that complement-mediated serum cytotoxicity assessment does not provide extra insight compared to anti-AQP4 Ab serum concentration. Furthermore, none of these parameters appears closely related to disease activity and/or severity. Therefore, in clinical practice, serum anti-AQP4 reactivity seems not helpful as a predictive biomarker in the followup of NMO patients as a means of predicting the onset of a relapse and adapting the treatment accordingly.
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spelling pubmed-36554572013-05-24 Evaluation of Clinical Interest of Anti-Aquaporin-4 Autoantibody Followup in Neuromyelitis Optica Chanson, Jean-Baptiste Alame, Melissa Collongues, Nicolas Blanc, Frédéric Fleury, Marie Rudolf, Gabrielle de Seze, Jérôme Vincent, Thierry Clin Dev Immunol Research Article Neuromyelitis optica (NMO) is an autoimmune disease in which a specific biomarker named NMO-IgG and directed against aquaporin-4 (AQP4) has been found. A correlation between disease activity and anti-AQP4 antibody (Ab) serum concentration or complement-mediated cytotoxicity has been reported, but the usefulness of longitudinal evaluation of these parameters remains to be evaluated in actual clinical practice. Thirty serum samples from 10 NMO patients positive for NMO-IgG were collected from 2006 to 2011. Anti-AQP4 Ab serum concentration and complement-mediated cytotoxicity were measured by flow cytometry using two quantitative cell-based assays (CBA) and compared with clinical parameters. We found a strong correlation between serum anti-AQP4 Ab concentration and complement-mediated cytotoxicity (P < 0.0001). Nevertheless, neither relapse nor worsening of impairment level was closely associated with a significant increase in serum Ab concentration or cytotoxicity. These results suggest that complement-mediated serum cytotoxicity assessment does not provide extra insight compared to anti-AQP4 Ab serum concentration. Furthermore, none of these parameters appears closely related to disease activity and/or severity. Therefore, in clinical practice, serum anti-AQP4 reactivity seems not helpful as a predictive biomarker in the followup of NMO patients as a means of predicting the onset of a relapse and adapting the treatment accordingly. Hindawi Publishing Corporation 2013 2013-04-28 /pmc/articles/PMC3655457/ /pubmed/23710199 http://dx.doi.org/10.1155/2013/146219 Text en Copyright © 2013 Jean-Baptiste Chanson et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Chanson, Jean-Baptiste
Alame, Melissa
Collongues, Nicolas
Blanc, Frédéric
Fleury, Marie
Rudolf, Gabrielle
de Seze, Jérôme
Vincent, Thierry
Evaluation of Clinical Interest of Anti-Aquaporin-4 Autoantibody Followup in Neuromyelitis Optica
title Evaluation of Clinical Interest of Anti-Aquaporin-4 Autoantibody Followup in Neuromyelitis Optica
title_full Evaluation of Clinical Interest of Anti-Aquaporin-4 Autoantibody Followup in Neuromyelitis Optica
title_fullStr Evaluation of Clinical Interest of Anti-Aquaporin-4 Autoantibody Followup in Neuromyelitis Optica
title_full_unstemmed Evaluation of Clinical Interest of Anti-Aquaporin-4 Autoantibody Followup in Neuromyelitis Optica
title_short Evaluation of Clinical Interest of Anti-Aquaporin-4 Autoantibody Followup in Neuromyelitis Optica
title_sort evaluation of clinical interest of anti-aquaporin-4 autoantibody followup in neuromyelitis optica
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3655457/
https://www.ncbi.nlm.nih.gov/pubmed/23710199
http://dx.doi.org/10.1155/2013/146219
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