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Autoantibodies in Wilson disease: Impact on clinical course

Symptoms of Wilson disease (WD) vary and additional factors such as autoimmunity may play an important role in WD pathogenesis. The presence of antinuclear antibodies (ANA), anti‐neutrophil cytoplasmic antibodies, neuronal surface antibodies, and onconeural antibodies in WD was investigated using st...

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Autores principales: Antczak‐Kowalska, Magdalena, Członkowska, Anna, Eyileten, Ceren, Palejko, Anna, Cudna, Agnieszka, Wolska, Marta, Piechal, Agnieszka, Litwin, Tomasz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9458613/
https://www.ncbi.nlm.nih.gov/pubmed/36101827
http://dx.doi.org/10.1002/jmd2.12317
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author Antczak‐Kowalska, Magdalena
Członkowska, Anna
Eyileten, Ceren
Palejko, Anna
Cudna, Agnieszka
Wolska, Marta
Piechal, Agnieszka
Litwin, Tomasz
author_facet Antczak‐Kowalska, Magdalena
Członkowska, Anna
Eyileten, Ceren
Palejko, Anna
Cudna, Agnieszka
Wolska, Marta
Piechal, Agnieszka
Litwin, Tomasz
author_sort Antczak‐Kowalska, Magdalena
collection PubMed
description Symptoms of Wilson disease (WD) vary and additional factors such as autoimmunity may play an important role in WD pathogenesis. The presence of antinuclear antibodies (ANA), anti‐neutrophil cytoplasmic antibodies, neuronal surface antibodies, and onconeural antibodies in WD was investigated using standardized indirect immunofluorescence assays and Western Blot analysis. The presence of all studied autoantibodies was higher in WD patients in comparison to healthy subjects, but there was no statistically significant difference in autoantibodies frequency according to disease manifestation. D‐penicillamine treatment was associated with a higher presence of ANA than zinc sulfate but without an increase in autoimmune diseases rate.
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spelling pubmed-94586132022-09-12 Autoantibodies in Wilson disease: Impact on clinical course Antczak‐Kowalska, Magdalena Członkowska, Anna Eyileten, Ceren Palejko, Anna Cudna, Agnieszka Wolska, Marta Piechal, Agnieszka Litwin, Tomasz JIMD Rep Research Reports Symptoms of Wilson disease (WD) vary and additional factors such as autoimmunity may play an important role in WD pathogenesis. The presence of antinuclear antibodies (ANA), anti‐neutrophil cytoplasmic antibodies, neuronal surface antibodies, and onconeural antibodies in WD was investigated using standardized indirect immunofluorescence assays and Western Blot analysis. The presence of all studied autoantibodies was higher in WD patients in comparison to healthy subjects, but there was no statistically significant difference in autoantibodies frequency according to disease manifestation. D‐penicillamine treatment was associated with a higher presence of ANA than zinc sulfate but without an increase in autoimmune diseases rate. John Wiley & Sons, Inc. 2022-07-22 /pmc/articles/PMC9458613/ /pubmed/36101827 http://dx.doi.org/10.1002/jmd2.12317 Text en © 2022 The Authors. JIMD Reports published by John Wiley & Sons Ltd on behalf of SSIEM. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Reports
Antczak‐Kowalska, Magdalena
Członkowska, Anna
Eyileten, Ceren
Palejko, Anna
Cudna, Agnieszka
Wolska, Marta
Piechal, Agnieszka
Litwin, Tomasz
Autoantibodies in Wilson disease: Impact on clinical course
title Autoantibodies in Wilson disease: Impact on clinical course
title_full Autoantibodies in Wilson disease: Impact on clinical course
title_fullStr Autoantibodies in Wilson disease: Impact on clinical course
title_full_unstemmed Autoantibodies in Wilson disease: Impact on clinical course
title_short Autoantibodies in Wilson disease: Impact on clinical course
title_sort autoantibodies in wilson disease: impact on clinical course
topic Research Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9458613/
https://www.ncbi.nlm.nih.gov/pubmed/36101827
http://dx.doi.org/10.1002/jmd2.12317
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