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Autoantibody Profiling and Anti-Kinesin Reactivity in ANCA-Associated Vasculitis

ANCA-associated vasculitides (AAV) are rare autoimmune diseases causing inflammation and damage to small blood vessels. New autoantibody biomarkers are needed to improve the diagnosis and treatment of AAV patients. In this study, we aimed to profile the autoantibody repertoire of AAV patients using...

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Autores principales: Mescia, Federica, Bayati, Shaghayegh, Brouwer, Elisabeth, Heeringa, Peter, Toonen, Erik J. M., Beenes, Marijke, Ball, Miriam J., Rees, Andrew J., Kain, Renate, Lyons, Paul A., Nilsson, Peter, Pin, Elisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10607136/
https://www.ncbi.nlm.nih.gov/pubmed/37895021
http://dx.doi.org/10.3390/ijms242015341
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author Mescia, Federica
Bayati, Shaghayegh
Brouwer, Elisabeth
Heeringa, Peter
Toonen, Erik J. M.
Beenes, Marijke
Ball, Miriam J.
Rees, Andrew J.
Kain, Renate
Lyons, Paul A.
Nilsson, Peter
Pin, Elisa
author_facet Mescia, Federica
Bayati, Shaghayegh
Brouwer, Elisabeth
Heeringa, Peter
Toonen, Erik J. M.
Beenes, Marijke
Ball, Miriam J.
Rees, Andrew J.
Kain, Renate
Lyons, Paul A.
Nilsson, Peter
Pin, Elisa
author_sort Mescia, Federica
collection PubMed
description ANCA-associated vasculitides (AAV) are rare autoimmune diseases causing inflammation and damage to small blood vessels. New autoantibody biomarkers are needed to improve the diagnosis and treatment of AAV patients. In this study, we aimed to profile the autoantibody repertoire of AAV patients using in-house developed antigen arrays to identify previously unreported antibodies linked to the disease per se, clinical subgroups, or clinical activity. A total of 1743 protein fragments representing 1561 unique proteins were screened in 229 serum samples collected from 137 AAV patients at presentation, remission, and relapse. Additionally, serum samples from healthy individuals and patients with other type of vasculitis and autoimmune-inflammatory conditions were included to evaluate the specificity of the autoantibodies identified in AAV. Autoreactivity against members of the kinesin protein family were identified in AAV patients, healthy volunteers, and disease controls. Anti-KIF4A antibodies were significantly more prevalent in AAV. We also observed possible associations between anti-kinesin antibodies and clinically relevant features within AAV patients. Further verification studies will be needed to confirm these findings.
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spelling pubmed-106071362023-10-28 Autoantibody Profiling and Anti-Kinesin Reactivity in ANCA-Associated Vasculitis Mescia, Federica Bayati, Shaghayegh Brouwer, Elisabeth Heeringa, Peter Toonen, Erik J. M. Beenes, Marijke Ball, Miriam J. Rees, Andrew J. Kain, Renate Lyons, Paul A. Nilsson, Peter Pin, Elisa Int J Mol Sci Article ANCA-associated vasculitides (AAV) are rare autoimmune diseases causing inflammation and damage to small blood vessels. New autoantibody biomarkers are needed to improve the diagnosis and treatment of AAV patients. In this study, we aimed to profile the autoantibody repertoire of AAV patients using in-house developed antigen arrays to identify previously unreported antibodies linked to the disease per se, clinical subgroups, or clinical activity. A total of 1743 protein fragments representing 1561 unique proteins were screened in 229 serum samples collected from 137 AAV patients at presentation, remission, and relapse. Additionally, serum samples from healthy individuals and patients with other type of vasculitis and autoimmune-inflammatory conditions were included to evaluate the specificity of the autoantibodies identified in AAV. Autoreactivity against members of the kinesin protein family were identified in AAV patients, healthy volunteers, and disease controls. Anti-KIF4A antibodies were significantly more prevalent in AAV. We also observed possible associations between anti-kinesin antibodies and clinically relevant features within AAV patients. Further verification studies will be needed to confirm these findings. MDPI 2023-10-19 /pmc/articles/PMC10607136/ /pubmed/37895021 http://dx.doi.org/10.3390/ijms242015341 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Mescia, Federica
Bayati, Shaghayegh
Brouwer, Elisabeth
Heeringa, Peter
Toonen, Erik J. M.
Beenes, Marijke
Ball, Miriam J.
Rees, Andrew J.
Kain, Renate
Lyons, Paul A.
Nilsson, Peter
Pin, Elisa
Autoantibody Profiling and Anti-Kinesin Reactivity in ANCA-Associated Vasculitis
title Autoantibody Profiling and Anti-Kinesin Reactivity in ANCA-Associated Vasculitis
title_full Autoantibody Profiling and Anti-Kinesin Reactivity in ANCA-Associated Vasculitis
title_fullStr Autoantibody Profiling and Anti-Kinesin Reactivity in ANCA-Associated Vasculitis
title_full_unstemmed Autoantibody Profiling and Anti-Kinesin Reactivity in ANCA-Associated Vasculitis
title_short Autoantibody Profiling and Anti-Kinesin Reactivity in ANCA-Associated Vasculitis
title_sort autoantibody profiling and anti-kinesin reactivity in anca-associated vasculitis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10607136/
https://www.ncbi.nlm.nih.gov/pubmed/37895021
http://dx.doi.org/10.3390/ijms242015341
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