Association between Multiple Sclerosis and FOXP3 Gene Promoter Region Mutations
Abstract
Regulatory T-Cells (Treg Cells), as one of the immune system components, have been highly effective in the autoimmune diseases prevention, particularly multiple sclerosis (MS). MS is a chronic inflammatory and autoimmune disease characterized by immune infiltration and inflammation in the central nervous system. Regulatory T (Treg) cells play an important role in the control of autoimmunity. Expression and action of the transcription factor FOXP3 controls the development and function of Treg cell. The aim of this study was to investigate the association between MS and FOXP3 gene promoter region polymorphisms rs2232365 (-924A/G) and rs3761548 (-3279A/C) in a Turkish population. In this case-control study we investigated these polymorphisms in 80 MS patients and 80 healthy controls using PCR-RFLP methods.
Results of our study showed that while there is significant correlation between MS and FOXP3 rs3761548 polymorphism (p=0.031), FOXP3 rs2232365 polymorphism, has not been found to be associated with the disease (p=0.31). As FOXP3 gene is one of the most important genes in the regulation of the immune cells, it may be concluded that the expression of this gene is important in MS patients. As this SNP is located in the promoter region of the gene, it may affect the expression level of FOXP3 protein.
Keywords
References
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Details
Primary Language
English
Subjects
Health Care Administration
Journal Section
Research Article
Authors
Nilgun Cekin
Türkiye
Ergun Pinarbasi
*
Türkiye
Aslihan Esra Bildirici
Türkiye
Seyda Akin
Türkiye
Ozlem Kayim Yildiz
Türkiye
Publication Date
September 30, 2018
Submission Date
April 27, 2018
Acceptance Date
July 4, 2018
Published in Issue
Year 1970 Volume: 40 Number: 3
Cited By
Association of FOXP3 Polymorphisms with Susceptibility to Multiple Sclerosis: A Meta-Analysis on Genetic Association Studies
Current Pharmacogenomics and Personalized Medicine
https://doi.org/10.2174/1875692118666200122163559