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Antibodies to a strain-specific citrullinated Epstein-Barr virus peptide diagnoses rheumatoid arthritis

Rheumatoid arthritis (RA) is a chronic systemic autoimmune disease. Anti-citrullinated protein antibodies (ACPA) are crucial for the serological diagnosis of RA, where Epstein-Barr virus (EBV) has been suggested to be an environmental agent in triggering the onset of the disease. This study aimed to...

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Autores principales: Trier, Nicole Hartwig, Holm, Bettina Eide, Heiden, Julie, Slot, Ole, Locht, Henning, Lindegaard, Hanne, Svendsen, Anders, Nielsen, Christoffer Tandrup, Jacobsen, Søren, Theander, Elke, Houen, Gunnar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5829227/
https://www.ncbi.nlm.nih.gov/pubmed/29487382
http://dx.doi.org/10.1038/s41598-018-22058-6
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author Trier, Nicole Hartwig
Holm, Bettina Eide
Heiden, Julie
Slot, Ole
Locht, Henning
Lindegaard, Hanne
Svendsen, Anders
Nielsen, Christoffer Tandrup
Jacobsen, Søren
Theander, Elke
Houen, Gunnar
author_facet Trier, Nicole Hartwig
Holm, Bettina Eide
Heiden, Julie
Slot, Ole
Locht, Henning
Lindegaard, Hanne
Svendsen, Anders
Nielsen, Christoffer Tandrup
Jacobsen, Søren
Theander, Elke
Houen, Gunnar
author_sort Trier, Nicole Hartwig
collection PubMed
description Rheumatoid arthritis (RA) is a chronic systemic autoimmune disease. Anti-citrullinated protein antibodies (ACPA) are crucial for the serological diagnosis of RA, where Epstein-Barr virus (EBV) has been suggested to be an environmental agent in triggering the onset of the disease. This study aimed to analyse antibody reactivity to citrullinated EBV nuclear antigen-2 (EBNA-2) peptides from three different EBV strains (B95-8, GD1 and AG876) using streptavidin capture enzyme-linked immunosorbent assay. One peptide, only found in a single strain (AG876), obtained a sensitivity and specificity of 77% and 95%, respectively and showed high sequence similarity to the filaggrin peptide originally used for ACPA detection. Comparison of antibody reactivity to commercial assays found that the citrullinated peptide was as effective in detecting ACPA as highly sensitive and specific commercial assays. The data presented demonstrate that the citrullinated EBNA-2 peptide indeed is recognised specifically by RA sera and that the single peptide is able to compete with assays containing multiple peptides. Furthermore, it could be hypothesized that RA may be caused by (a) specific strain(s) of EBV.
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spelling pubmed-58292272018-03-01 Antibodies to a strain-specific citrullinated Epstein-Barr virus peptide diagnoses rheumatoid arthritis Trier, Nicole Hartwig Holm, Bettina Eide Heiden, Julie Slot, Ole Locht, Henning Lindegaard, Hanne Svendsen, Anders Nielsen, Christoffer Tandrup Jacobsen, Søren Theander, Elke Houen, Gunnar Sci Rep Article Rheumatoid arthritis (RA) is a chronic systemic autoimmune disease. Anti-citrullinated protein antibodies (ACPA) are crucial for the serological diagnosis of RA, where Epstein-Barr virus (EBV) has been suggested to be an environmental agent in triggering the onset of the disease. This study aimed to analyse antibody reactivity to citrullinated EBV nuclear antigen-2 (EBNA-2) peptides from three different EBV strains (B95-8, GD1 and AG876) using streptavidin capture enzyme-linked immunosorbent assay. One peptide, only found in a single strain (AG876), obtained a sensitivity and specificity of 77% and 95%, respectively and showed high sequence similarity to the filaggrin peptide originally used for ACPA detection. Comparison of antibody reactivity to commercial assays found that the citrullinated peptide was as effective in detecting ACPA as highly sensitive and specific commercial assays. The data presented demonstrate that the citrullinated EBNA-2 peptide indeed is recognised specifically by RA sera and that the single peptide is able to compete with assays containing multiple peptides. Furthermore, it could be hypothesized that RA may be caused by (a) specific strain(s) of EBV. Nature Publishing Group UK 2018-02-27 /pmc/articles/PMC5829227/ /pubmed/29487382 http://dx.doi.org/10.1038/s41598-018-22058-6 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Trier, Nicole Hartwig
Holm, Bettina Eide
Heiden, Julie
Slot, Ole
Locht, Henning
Lindegaard, Hanne
Svendsen, Anders
Nielsen, Christoffer Tandrup
Jacobsen, Søren
Theander, Elke
Houen, Gunnar
Antibodies to a strain-specific citrullinated Epstein-Barr virus peptide diagnoses rheumatoid arthritis
title Antibodies to a strain-specific citrullinated Epstein-Barr virus peptide diagnoses rheumatoid arthritis
title_full Antibodies to a strain-specific citrullinated Epstein-Barr virus peptide diagnoses rheumatoid arthritis
title_fullStr Antibodies to a strain-specific citrullinated Epstein-Barr virus peptide diagnoses rheumatoid arthritis
title_full_unstemmed Antibodies to a strain-specific citrullinated Epstein-Barr virus peptide diagnoses rheumatoid arthritis
title_short Antibodies to a strain-specific citrullinated Epstein-Barr virus peptide diagnoses rheumatoid arthritis
title_sort antibodies to a strain-specific citrullinated epstein-barr virus peptide diagnoses rheumatoid arthritis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5829227/
https://www.ncbi.nlm.nih.gov/pubmed/29487382
http://dx.doi.org/10.1038/s41598-018-22058-6
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