TNF-α -308G/A gene polymorphism in bullous pemphigoid and alopecia areata

Hamideh Moravvej, Pardis Sadat Tabatabaei-Panah, Elaheh Ebrahimi, Nafiseh Esmaeili, Sayyed Mohammad Hossein Ghaderian, Ralf J. Ludwig, Reza Akbarzadeh*

*Corresponding author for this work

Abstract

Background: TNF-α -308G/A polymorphism has been investigated in few studies for an association with susceptibility to bullous pemphigoid (BP) and alopecia areata (AA). Yet, these findings had so far not been independently replicated, and no data on a possible association of TNFα -308G/A polymorphism with these diseases in Iranian population were available. Objectives: In the present study, a possible effect of TNF-α -308G/A variation on susceptibility to BP or AA disease was evaluated. Methods: Genomic DNA was extracted from the blood of the patients with BP and AA as well as control subjects which genotyped for the TNF-α -308 G/A polymorphism. TNF-α gene expression levels were analyzed by real-time RT-PCR. Results: No association was observed between the TNF-α -308 G/A variation and susceptibility to BP or AA diseases in our Iranian cohort. In contrast to AA patients, expression of TNF-α gene was significantly higher in BP patients compared to control group. TNF-α gene was found to be similarly expressed in mutant and wild-type genotypes. Conclusions: TNF-α -308G/A polymorphism is not associated with the risk to develop of BP and AA in our Iranian cohort. Furthermore, this polymorphism is contributed to altering the levels of gene expression in BP disease.

Original languageEnglish
JournalHuman Antibodies
Volume26
Issue number4
Pages (from-to)201-207
Number of pages7
ISSN1093-2607
DOIs
Publication statusPublished - 01.01.2018

Fingerprint

Dive into the research topics of 'TNF-α -308G/A gene polymorphism in bullous pemphigoid and alopecia areata'. Together they form a unique fingerprint.

Cite this