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Hum Antibodies ; 26(4): 219-224, 2018.
Article in English | MEDLINE | ID: mdl-29889063

ABSTRACT

Multiple sclerosis (MS) is an autoimmune disease characterized by recurrent episodes of demyelination and loss of oligodendrocytes. The demyelination process is caused by various subsets of CD4+ T cells with a Th1 and Th17 phenotype. The retinoid acid-related orphan receptor A (RORA) is expressed in Th17 cells and promote Th17 differentiation. In this study, we compared the expression level of RORA gene in the blood of 50 relapsing-remitting MS (RRMS) patients who were treated with IFN-ß and 50 healthy controls by TaqMan Quantitative Real-Time PCR.We found that RORA expression was significantly down-regulated in MS patients compared with controls (P= 0.006). However, there was no significant correlation between RORA gene expression and Kurtzke Expanded Disability Status Scale (EDSS). Our findings suggest a possible contribution of IFN-ß in the downregulation of RORA. In addition, RORA downregulation may be a potential indicator of positive response to interferon beta treatment of multiple sclerosis patients.


Subject(s)
Multiple Sclerosis, Relapsing-Remitting/blood , Nuclear Receptor Subfamily 1, Group F, Member 1/blood , Adult , Age of Onset , Case-Control Studies , Disability Evaluation , Down-Regulation , Female , Humans , Interferon-alpha/therapeutic use , Interferon-beta/metabolism , Male , Multiple Sclerosis, Relapsing-Remitting/genetics , Nuclear Receptor Subfamily 1, Group F, Member 1/genetics , Real-Time Polymerase Chain Reaction , Th17 Cells
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