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: Gisela Nogales-Gadea, Alba Ramos-Fransi, Xavier Suárez-Calvet, Miquel Navas, Ricard Rojas-García, Jose Luis Mosquera, Jordi Díaz-Manera, Luis Querol, Eduard Gallardo, Isabel Illa
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Publicado: Public Library of Science (PLoS) 2014
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spelling oai:doaj.org-article:680a1d439c5c465e996a66ad2745698b2021-11-18T08:27:51ZAnalysis of serum miRNA profiles of myasthenia gravis patients.1932-620310.1371/journal.pone.0091927https://doaj.org/article/680a1d439c5c465e996a66ad2745698b2014-01-01T00:00:00Zhttps://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24637658/pdf/?tool=EBIhttps://doaj.org/toc/1932-6203Myasthenia 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.Gisela Nogales-GadeaAlba Ramos-FransiXavier Suárez-CalvetMiquel NavasRicard Rojas-GarcíaJose Luis MosqueraJordi Díaz-ManeraLuis QuerolEduard GallardoIsabel IllaPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 9, Iss 3, p e91927 (2014)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Gisela Nogales-Gadea
Alba Ramos-Fransi
Xavier Suárez-Calvet
Miquel Navas
Ricard Rojas-García
Jose Luis Mosquera
Jordi Díaz-Manera
Luis Querol
Eduard Gallardo
Isabel Illa
Analysis of serum miRNA profiles of myasthenia gravis patients.
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.
format article
author Gisela Nogales-Gadea
Alba Ramos-Fransi
Xavier Suárez-Calvet
Miquel Navas
Ricard Rojas-García
Jose Luis Mosquera
Jordi Díaz-Manera
Luis Querol
Eduard Gallardo
Isabel Illa
author_facet Gisela Nogales-Gadea
Alba Ramos-Fransi
Xavier Suárez-Calvet
Miquel Navas
Ricard Rojas-García
Jose Luis Mosquera
Jordi Díaz-Manera
Luis Querol
Eduard Gallardo
Isabel Illa
author_sort Gisela Nogales-Gadea
title Analysis of serum miRNA profiles of myasthenia gravis patients.
title_short 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_sort analysis of serum mirna profiles of myasthenia gravis patients.
publisher Public Library of Science (PLoS)
publishDate 2014
url https://doaj.org/article/680a1d439c5c465e996a66ad2745698b
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