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New autoantibodies in early rheumatoid arthritis
INTRODUCTION: Rheumatoid arthritis (RA) is a chronic inflammatory joint disease causing articular cartilage and bone destruction. Since irreversible joint destruction can be prevented by intervention at the early stages of disease, early diagnosis of RA is important. In this study, we identified new...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3978570/ https://www.ncbi.nlm.nih.gov/pubmed/23886014 http://dx.doi.org/10.1186/ar4255 |
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author | Charpin, Caroline Arnoux, Fanny Martin, Marielle Toussirot, Eric Lambert, Nathalie Balandraud, Nathalie Wendling, Daniel Diot, Elisabeth Roudier, Jean Auger, Isabelle |
author_facet | Charpin, Caroline Arnoux, Fanny Martin, Marielle Toussirot, Eric Lambert, Nathalie Balandraud, Nathalie Wendling, Daniel Diot, Elisabeth Roudier, Jean Auger, Isabelle |
author_sort | Charpin, Caroline |
collection | PubMed |
description | INTRODUCTION: Rheumatoid arthritis (RA) is a chronic inflammatory joint disease causing articular cartilage and bone destruction. Since irreversible joint destruction can be prevented by intervention at the early stages of disease, early diagnosis of RA is important. In this study, we identified new autoantibodies in the sera of patients with early (less than one year) RA. METHODS: We screened the sera of 20 RA patients with disease duration less than one year, 19 RA patients with disease duration more than five years and 23 controls on 8,268 human protein arrays. We confirmed the validity of protein array detection by ELISA assays. We then performed epitope mapping with overlapping 15-mers to analyze RA sera reactivity. RESULTS: WIBG (within BGCN homolog (Drosophila)), GABARAPL2 (GABA(A) receptor associated protein like 2) and ZNF706 (zinc finger protein 706) proteins are preferentially recognized by autoantibodies from early RA patients. Of interest, autoantibodies to WIBG are very specific for early RA. Indeed, 33% of early RA patients' sera recognize WIBG versus 5% of RA patients with disease duration more than 5 years and 2% of controls. We identified three linear peptides on WIBG GABARAPL2 and ZNF706 that are preferentially recognized by sera of early RA patients. CONCLUSIONS: We identified new autoantibodies associated with RA with disease duration less than one year. These autoantibodies could be used as diagnosis markers in RA patients. |
format | Online Article Text |
id | pubmed-3978570 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-39785702014-04-09 New autoantibodies in early rheumatoid arthritis Charpin, Caroline Arnoux, Fanny Martin, Marielle Toussirot, Eric Lambert, Nathalie Balandraud, Nathalie Wendling, Daniel Diot, Elisabeth Roudier, Jean Auger, Isabelle Arthritis Res Ther Research Article INTRODUCTION: Rheumatoid arthritis (RA) is a chronic inflammatory joint disease causing articular cartilage and bone destruction. Since irreversible joint destruction can be prevented by intervention at the early stages of disease, early diagnosis of RA is important. In this study, we identified new autoantibodies in the sera of patients with early (less than one year) RA. METHODS: We screened the sera of 20 RA patients with disease duration less than one year, 19 RA patients with disease duration more than five years and 23 controls on 8,268 human protein arrays. We confirmed the validity of protein array detection by ELISA assays. We then performed epitope mapping with overlapping 15-mers to analyze RA sera reactivity. RESULTS: WIBG (within BGCN homolog (Drosophila)), GABARAPL2 (GABA(A) receptor associated protein like 2) and ZNF706 (zinc finger protein 706) proteins are preferentially recognized by autoantibodies from early RA patients. Of interest, autoantibodies to WIBG are very specific for early RA. Indeed, 33% of early RA patients' sera recognize WIBG versus 5% of RA patients with disease duration more than 5 years and 2% of controls. We identified three linear peptides on WIBG GABARAPL2 and ZNF706 that are preferentially recognized by sera of early RA patients. CONCLUSIONS: We identified new autoantibodies associated with RA with disease duration less than one year. These autoantibodies could be used as diagnosis markers in RA patients. BioMed Central 2013 2013-07-25 /pmc/articles/PMC3978570/ /pubmed/23886014 http://dx.doi.org/10.1186/ar4255 Text en Copyright © 2013 Charpin et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Charpin, Caroline Arnoux, Fanny Martin, Marielle Toussirot, Eric Lambert, Nathalie Balandraud, Nathalie Wendling, Daniel Diot, Elisabeth Roudier, Jean Auger, Isabelle New autoantibodies in early rheumatoid arthritis |
title | New autoantibodies in early rheumatoid arthritis |
title_full | New autoantibodies in early rheumatoid arthritis |
title_fullStr | New autoantibodies in early rheumatoid arthritis |
title_full_unstemmed | New autoantibodies in early rheumatoid arthritis |
title_short | New autoantibodies in early rheumatoid arthritis |
title_sort | new autoantibodies in early rheumatoid arthritis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3978570/ https://www.ncbi.nlm.nih.gov/pubmed/23886014 http://dx.doi.org/10.1186/ar4255 |
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