Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/110396
Title: Transcriptome Analysis Describing New Immunity and Defense Genes in Peripheral Blood Mononuclear Cells of Rheumatoid Arthritis Patients
Authors: Teixeira, Vitor Hugo 
Olaso, Robert
Martin-Magniette, Marie-Laure
Lasbleiz, Sandra 
Jacq, Laurent 
Oliveira, Catarina Resende 
Hilliquin, Pascal 
Gut, Ivo
Cornélis, François 
Petit-Teixeira, Elisabeth 
Issue Date: 2009
Publisher: Public Library of Science
Project: Association Franc¸aise des Polyarthritiques, Socie´te´ Franc¸aise de Rhumatologie, Association Rhumatisme et Travail, European Union for AutoCure, Association Polyarctique, Agence Franc¸aise de Se´curite´ Sanitaire des Produits de Sante´ , Groupe Taitbout, Genopole, Federation Franc¸aise de Cardiologie, Societe Francaise de Cardiologie, Boehringer Ingelheim and the French Ministry of Research and Education 
SFRH/BD/23304/2005 
Serial title, monograph or event: PLoS ONE
Volume: 4
Issue: 8
Abstract: Background: Large-scale gene expression profiling of peripheral blood mononuclear cells from Rheumatoid Arthritis (RA) patients could provide a molecular description that reflects the contribution of diverse cellular responses associated with this disease. The aim of our study was to identify peripheral blood gene expression profiles for RA patients, using Illumina technology, to gain insights into RA molecular mechanisms. Methodology/Principal Findings: The Illumina Human-6v2 Expression BeadChips were used for a complete genome-wide transcript profiling of peripheral blood mononuclear cells (PBMCs) from 18 RA patients and 15 controls. Differential analysis per gene was performed with one-way analysis of variance (ANOVA) and P values were adjusted to control the False Discovery Rate (FDR,5%). Genes differentially expressed at significant level between patients and controls were analyzed using Gene Ontology (GO) in the PANTHER database to identify biological processes. A differentially expression of 339 Reference Sequence genes (238 down-regulated and 101 up-regulated) between the two groups was observed. We identified a remarkably elevated expression of a spectrum of genes involved in Immunity and Defense in PBMCs of RA patients compared to controls. This result is confirmed by GO analysis, suggesting that these genes could be activated systemically in RA. No significant down-regulated ontology groups were found. Microarray data were validated by real time PCR in a set of nine genes showing a high degree of correlation. Conclusions/Significance: Our study highlighted several new genes that could contribute in the identification of innovative clinical biomarkers for diagnostic procedures and therapeutic interventions.
URI: https://hdl.handle.net/10316/110396
ISSN: 1932-6203
DOI: 10.1371/journal.pone.0006803
Rights: openAccess
Appears in Collections:FMUC Medicina - Artigos em Revistas Internacionais
I&D CNC - Artigos em Revistas Internacionais

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