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Antibodies against 4 Atypical Post-Translational Protein Modifications in Patients with Rheumatoid Arthritis
Patients with rheumatoid arthritis (RA) show autoantibodies against post-translational protein modifications (PTMs), such as anti-citrullinated protein antibodies. However, the range of recognized PTMs is unknown. Here, we addressed four PTMs: chlorination, non-enzymatic glycation, nitration, and ho...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8870974/ https://www.ncbi.nlm.nih.gov/pubmed/35204444 http://dx.doi.org/10.3390/diagnostics12020352 |
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author | Rodríguez-Martínez, Lorena Regueiro, Cristina Amhaz-Escanlar, Sámer Pena, Carmen Herbello-Hermelo, Paloma Moreda-Piñeiro, Antonio Rodriguez-Garcia, Javier Mera-Varela, Antonio Pérez-Pampín, Eva González, Antonio |
author_facet | Rodríguez-Martínez, Lorena Regueiro, Cristina Amhaz-Escanlar, Sámer Pena, Carmen Herbello-Hermelo, Paloma Moreda-Piñeiro, Antonio Rodriguez-Garcia, Javier Mera-Varela, Antonio Pérez-Pampín, Eva González, Antonio |
author_sort | Rodríguez-Martínez, Lorena |
collection | PubMed |
description | Patients with rheumatoid arthritis (RA) show autoantibodies against post-translational protein modifications (PTMs), such as anti-citrullinated protein antibodies. However, the range of recognized PTMs is unknown. Here, we addressed four PTMs: chlorination, non-enzymatic glycation, nitration, and homocysteinylation, identified as targets of atypical RA autoantibodies in studies whose protocols we have followed. The modified antigens included collagen type II, an extract of synovial proteins and a selection of peptides. We interpreted the results according to the optical density (OD) obtained in an enzyme-linked immunosorbent assay ( ELISA) with the modified antigen and the corrected OD obtained after subtracting the reactivity against the unmodified antigen. The results showed evidence of specific antibodies against glycated collagen type II, as the corrected ODs were higher in the 182 patients with RA than in the 164 healthy controls (p = 0.0003). However, the relevance of these antibodies was doubtful because the magnitude of the specific signal was small (median OD = 0.072 vs. 0.027, respectively). There were no specific antibodies against any of the other three PTMs. Therefore, our results showed that the four PTMs are not inducing a significant autoantibody response in patients with RA. These results indicated that the repertoire of PTM autoantigens in RA is restricted. |
format | Online Article Text |
id | pubmed-8870974 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-88709742022-02-25 Antibodies against 4 Atypical Post-Translational Protein Modifications in Patients with Rheumatoid Arthritis Rodríguez-Martínez, Lorena Regueiro, Cristina Amhaz-Escanlar, Sámer Pena, Carmen Herbello-Hermelo, Paloma Moreda-Piñeiro, Antonio Rodriguez-Garcia, Javier Mera-Varela, Antonio Pérez-Pampín, Eva González, Antonio Diagnostics (Basel) Article Patients with rheumatoid arthritis (RA) show autoantibodies against post-translational protein modifications (PTMs), such as anti-citrullinated protein antibodies. However, the range of recognized PTMs is unknown. Here, we addressed four PTMs: chlorination, non-enzymatic glycation, nitration, and homocysteinylation, identified as targets of atypical RA autoantibodies in studies whose protocols we have followed. The modified antigens included collagen type II, an extract of synovial proteins and a selection of peptides. We interpreted the results according to the optical density (OD) obtained in an enzyme-linked immunosorbent assay ( ELISA) with the modified antigen and the corrected OD obtained after subtracting the reactivity against the unmodified antigen. The results showed evidence of specific antibodies against glycated collagen type II, as the corrected ODs were higher in the 182 patients with RA than in the 164 healthy controls (p = 0.0003). However, the relevance of these antibodies was doubtful because the magnitude of the specific signal was small (median OD = 0.072 vs. 0.027, respectively). There were no specific antibodies against any of the other three PTMs. Therefore, our results showed that the four PTMs are not inducing a significant autoantibody response in patients with RA. These results indicated that the repertoire of PTM autoantigens in RA is restricted. MDPI 2022-01-29 /pmc/articles/PMC8870974/ /pubmed/35204444 http://dx.doi.org/10.3390/diagnostics12020352 Text en © 2022 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 Rodríguez-Martínez, Lorena Regueiro, Cristina Amhaz-Escanlar, Sámer Pena, Carmen Herbello-Hermelo, Paloma Moreda-Piñeiro, Antonio Rodriguez-Garcia, Javier Mera-Varela, Antonio Pérez-Pampín, Eva González, Antonio Antibodies against 4 Atypical Post-Translational Protein Modifications in Patients with Rheumatoid Arthritis |
title | Antibodies against 4 Atypical Post-Translational Protein Modifications in Patients with Rheumatoid Arthritis |
title_full | Antibodies against 4 Atypical Post-Translational Protein Modifications in Patients with Rheumatoid Arthritis |
title_fullStr | Antibodies against 4 Atypical Post-Translational Protein Modifications in Patients with Rheumatoid Arthritis |
title_full_unstemmed | Antibodies against 4 Atypical Post-Translational Protein Modifications in Patients with Rheumatoid Arthritis |
title_short | Antibodies against 4 Atypical Post-Translational Protein Modifications in Patients with Rheumatoid Arthritis |
title_sort | antibodies against 4 atypical post-translational protein modifications in patients with rheumatoid arthritis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8870974/ https://www.ncbi.nlm.nih.gov/pubmed/35204444 http://dx.doi.org/10.3390/diagnostics12020352 |
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