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Natural autoantibodies reactive with glycosaminoglycans in rheumatoid arthritis

INTRODUCTION: Although natural autoantibodies make up the majority of circulating immunoglobulins and are also present in high numbers in therapeutically used intravenous immunoglobulin preparations, they have received little attention and their precise role remains largely unknown. An increasing aw...

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Autores principales: György, Bence, Tóthfalusi, László, Nagy, György, Pásztói, Mária, Géher, Pál, Lörinc, Zsolt, Polgár, Anna, Rojkovich, Bernadett, Ujfalussy, Ilona, Poór, Gyula, Pócza, Péter, Wiener, Zoltán, Misják, Petra, Koncz, Agnes, Falus, András, Buzás, Edit I
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2592792/
https://www.ncbi.nlm.nih.gov/pubmed/18789149
http://dx.doi.org/10.1186/ar2507
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author György, Bence
Tóthfalusi, László
Nagy, György
Pásztói, Mária
Géher, Pál
Lörinc, Zsolt
Polgár, Anna
Rojkovich, Bernadett
Ujfalussy, Ilona
Poór, Gyula
Pócza, Péter
Wiener, Zoltán
Misják, Petra
Koncz, Agnes
Falus, András
Buzás, Edit I
author_facet György, Bence
Tóthfalusi, László
Nagy, György
Pásztói, Mária
Géher, Pál
Lörinc, Zsolt
Polgár, Anna
Rojkovich, Bernadett
Ujfalussy, Ilona
Poór, Gyula
Pócza, Péter
Wiener, Zoltán
Misják, Petra
Koncz, Agnes
Falus, András
Buzás, Edit I
author_sort György, Bence
collection PubMed
description INTRODUCTION: Although natural autoantibodies make up the majority of circulating immunoglobulins and are also present in high numbers in therapeutically used intravenous immunoglobulin preparations, they have received little attention and their precise role remains largely unknown. An increasing awareness of the importance of posttranslational autoantigen modifications and glycobiology led us to explore carbohydrate-reactive natural autoantibodies in patients with rheumatoid arthritis. This study examined systematic antibodies reactive to glycosaminoglycans (GAGs), the carbohydrate components of proteoglycans that are released in large amounts from degrading cartilage. METHODS: To measure antibodies reactive to six different types of GAGs, a specialised ELISA was used in which the carbohydrates were covalently linked to the plastic surface through a 2 nm spacer. Sera from rheumatoid arthritis patients (n = 66), umbilical cord serum samples (n = 11) and adult controls (n = 54) were studied. In order to explore cross-reactivity with microbial antigens, bacterial peptidoglycans and fungal polysaccharides were used. Sera and synovial fluid samples were also tested using a GlycoChip carbohydrate array to characterise individual carbohydrate recognition patterns. We followed a multistep statistical screening strategy for screening GAG-reactive antibodies as predictive disease markers. RESULTS: While anti-GAG antibodies were absent in the umbilical cord sera, they were readily detectable in adult controls and were significantly elevated in patients with rheumatoid arthritis (p < 0.001). Anti-GAG antibodies showed significant cross-reactivity among different types of GAGs. They also reacted with bacterial peptidoglycans and fungal polysaccharides. Interestingly, anti-chondroitin sulphate C IgM antibody levels showed inverse correlation both with the Disease Activity Score (DAS) 28 scores and C-reactive protein (CRP) levels in rheumatoid arthritis. CONCLUSION: The highly abundant and cross-reactive, GAG-specific natural autoantibodies in serum may serve as novel disease-state markers in patients with rheumatoid arthritis.
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spelling pubmed-25927922008-12-03 Natural autoantibodies reactive with glycosaminoglycans in rheumatoid arthritis György, Bence Tóthfalusi, László Nagy, György Pásztói, Mária Géher, Pál Lörinc, Zsolt Polgár, Anna Rojkovich, Bernadett Ujfalussy, Ilona Poór, Gyula Pócza, Péter Wiener, Zoltán Misják, Petra Koncz, Agnes Falus, András Buzás, Edit I Arthritis Res Ther Research Article INTRODUCTION: Although natural autoantibodies make up the majority of circulating immunoglobulins and are also present in high numbers in therapeutically used intravenous immunoglobulin preparations, they have received little attention and their precise role remains largely unknown. An increasing awareness of the importance of posttranslational autoantigen modifications and glycobiology led us to explore carbohydrate-reactive natural autoantibodies in patients with rheumatoid arthritis. This study examined systematic antibodies reactive to glycosaminoglycans (GAGs), the carbohydrate components of proteoglycans that are released in large amounts from degrading cartilage. METHODS: To measure antibodies reactive to six different types of GAGs, a specialised ELISA was used in which the carbohydrates were covalently linked to the plastic surface through a 2 nm spacer. Sera from rheumatoid arthritis patients (n = 66), umbilical cord serum samples (n = 11) and adult controls (n = 54) were studied. In order to explore cross-reactivity with microbial antigens, bacterial peptidoglycans and fungal polysaccharides were used. Sera and synovial fluid samples were also tested using a GlycoChip carbohydrate array to characterise individual carbohydrate recognition patterns. We followed a multistep statistical screening strategy for screening GAG-reactive antibodies as predictive disease markers. RESULTS: While anti-GAG antibodies were absent in the umbilical cord sera, they were readily detectable in adult controls and were significantly elevated in patients with rheumatoid arthritis (p < 0.001). Anti-GAG antibodies showed significant cross-reactivity among different types of GAGs. They also reacted with bacterial peptidoglycans and fungal polysaccharides. Interestingly, anti-chondroitin sulphate C IgM antibody levels showed inverse correlation both with the Disease Activity Score (DAS) 28 scores and C-reactive protein (CRP) levels in rheumatoid arthritis. CONCLUSION: The highly abundant and cross-reactive, GAG-specific natural autoantibodies in serum may serve as novel disease-state markers in patients with rheumatoid arthritis. BioMed Central 2008 2008-09-12 /pmc/articles/PMC2592792/ /pubmed/18789149 http://dx.doi.org/10.1186/ar2507 Text en Copyright © 2008 György 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
György, Bence
Tóthfalusi, László
Nagy, György
Pásztói, Mária
Géher, Pál
Lörinc, Zsolt
Polgár, Anna
Rojkovich, Bernadett
Ujfalussy, Ilona
Poór, Gyula
Pócza, Péter
Wiener, Zoltán
Misják, Petra
Koncz, Agnes
Falus, András
Buzás, Edit I
Natural autoantibodies reactive with glycosaminoglycans in rheumatoid arthritis
title Natural autoantibodies reactive with glycosaminoglycans in rheumatoid arthritis
title_full Natural autoantibodies reactive with glycosaminoglycans in rheumatoid arthritis
title_fullStr Natural autoantibodies reactive with glycosaminoglycans in rheumatoid arthritis
title_full_unstemmed Natural autoantibodies reactive with glycosaminoglycans in rheumatoid arthritis
title_short Natural autoantibodies reactive with glycosaminoglycans in rheumatoid arthritis
title_sort natural autoantibodies reactive with glycosaminoglycans in rheumatoid arthritis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2592792/
https://www.ncbi.nlm.nih.gov/pubmed/18789149
http://dx.doi.org/10.1186/ar2507
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