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Analysis of Serum miRNA Profiles of Myasthenia Gravis Patients

Myasthenia gravis (MG) is an autoimmune disease characterized by the presence of autoantibodies, mainly against the acetylcholine receptor (AChR). The mechanisms triggering and maintaining this chronic disease are unknown. MiRNAs are regulatory molecules that play a key role in the immune system and...

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Autores principales: Nogales-Gadea, Gisela, Ramos-Fransi, Alba, Suárez-Calvet, Xavier, Navas, Miquel, Rojas-García, Ricard, Mosquera, Jose Luis, Díaz-Manera, Jordi, Querol, Luis, Gallardo, Eduard, Illa, Isabel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3956820/
https://www.ncbi.nlm.nih.gov/pubmed/24637658
http://dx.doi.org/10.1371/journal.pone.0091927
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author Nogales-Gadea, Gisela
Ramos-Fransi, Alba
Suárez-Calvet, Xavier
Navas, Miquel
Rojas-García, Ricard
Mosquera, Jose Luis
Díaz-Manera, Jordi
Querol, Luis
Gallardo, Eduard
Illa, Isabel
author_facet Nogales-Gadea, Gisela
Ramos-Fransi, Alba
Suárez-Calvet, Xavier
Navas, Miquel
Rojas-García, Ricard
Mosquera, Jose Luis
Díaz-Manera, Jordi
Querol, Luis
Gallardo, Eduard
Illa, Isabel
author_sort Nogales-Gadea, Gisela
collection PubMed
description Myasthenia gravis (MG) is an autoimmune disease characterized by the presence of autoantibodies, mainly against the acetylcholine receptor (AChR). The mechanisms triggering and maintaining this chronic disease are unknown. MiRNAs are regulatory molecules that play a key role in the immune system and are altered in many autoimmune diseases. The aim of this study was to evaluate miRNA profiles in serum of 61 AChR MG patients. We studied serum from patients with early onset MG (n = 22), late onset MG (n = 27) and thymoma (n = 12), to identify alterations in the specific subgroups. In a discovery cohort, we analysed 381 miRNA arrays from 5 patients from each subgroup, and 5 healthy controls. The 15 patients had not received any treatment. We found 32 miRNAs in different levels in MG and analysed 8 of these in a validation cohort that included 46 of the MG patients. MiR15b, miR122, miR-140-3p, miR185, miR192, miR20b and miR-885-5p were in lower levels in MG patients than in controls. Our study suggests that different clinical phenotypes in MG share common altered mechanisms in circulating miRNAs, with no additional contribution of the thymoma. MG treatment intervention does not modify the profile of these miRNAs. Novel insights into the pathogenesis of MG can be reached by the analysis of circulating miRNAs since some of these miRNAs have also been found low in MG peripheral mononuclear cells, and have targets with important roles in B cell survival and antibody production.
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spelling pubmed-39568202014-03-18 Analysis of Serum miRNA Profiles of Myasthenia Gravis Patients Nogales-Gadea, Gisela Ramos-Fransi, Alba Suárez-Calvet, Xavier Navas, Miquel Rojas-García, Ricard Mosquera, Jose Luis Díaz-Manera, Jordi Querol, Luis Gallardo, Eduard Illa, Isabel PLoS One Research Article Myasthenia gravis (MG) is an autoimmune disease characterized by the presence of autoantibodies, mainly against the acetylcholine receptor (AChR). The mechanisms triggering and maintaining this chronic disease are unknown. MiRNAs are regulatory molecules that play a key role in the immune system and are altered in many autoimmune diseases. The aim of this study was to evaluate miRNA profiles in serum of 61 AChR MG patients. We studied serum from patients with early onset MG (n = 22), late onset MG (n = 27) and thymoma (n = 12), to identify alterations in the specific subgroups. In a discovery cohort, we analysed 381 miRNA arrays from 5 patients from each subgroup, and 5 healthy controls. The 15 patients had not received any treatment. We found 32 miRNAs in different levels in MG and analysed 8 of these in a validation cohort that included 46 of the MG patients. MiR15b, miR122, miR-140-3p, miR185, miR192, miR20b and miR-885-5p were in lower levels in MG patients than in controls. Our study suggests that different clinical phenotypes in MG share common altered mechanisms in circulating miRNAs, with no additional contribution of the thymoma. MG treatment intervention does not modify the profile of these miRNAs. Novel insights into the pathogenesis of MG can be reached by the analysis of circulating miRNAs since some of these miRNAs have also been found low in MG peripheral mononuclear cells, and have targets with important roles in B cell survival and antibody production. Public Library of Science 2014-03-17 /pmc/articles/PMC3956820/ /pubmed/24637658 http://dx.doi.org/10.1371/journal.pone.0091927 Text en © 2014 Nogales-Gadea et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Nogales-Gadea, Gisela
Ramos-Fransi, Alba
Suárez-Calvet, Xavier
Navas, Miquel
Rojas-García, Ricard
Mosquera, Jose Luis
Díaz-Manera, Jordi
Querol, Luis
Gallardo, Eduard
Illa, Isabel
Analysis of Serum miRNA Profiles of Myasthenia Gravis Patients
title Analysis of Serum miRNA Profiles of Myasthenia Gravis Patients
title_full Analysis of Serum miRNA Profiles of Myasthenia Gravis Patients
title_fullStr Analysis of Serum miRNA Profiles of Myasthenia Gravis Patients
title_full_unstemmed Analysis of Serum miRNA Profiles of Myasthenia Gravis Patients
title_short Analysis of Serum miRNA Profiles of Myasthenia Gravis Patients
title_sort analysis of serum mirna profiles of myasthenia gravis patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3956820/
https://www.ncbi.nlm.nih.gov/pubmed/24637658
http://dx.doi.org/10.1371/journal.pone.0091927
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