Search

This study has been conducted to evaluate the allele, genotype and haplotype frequencies of the polymorphic gene coding TGF-β in recurrent aphthous stomatitis (RAS). TGF-β gene typing was done by polymerase chain reaction with sequence-specific primers (PCR-SSP) assay. Allele frequencies were estimated by direct gene counting. C allele at codon 25 was significantly increased, while G allele at this position was significantly decreased in patients compared to the controls. A significantly higher frequency of CG genotype at codon 25 was found in control group. CC genotype and TT genotype at codon 10 of the gene was significantly decreased, while CT genotype at the same position was significantly increased in patients, indicating that CT heterozygosity at codon 10 TGF-β is associated with greater risk of RAS. CG and TG haplotypes were significantly decreased while CC and TC haplotypes were significantly increased in patients compared with controls. This study indicates the TGF-β single nucleotide polymorphisms could play a role in RAS pathogenesis. Thereby certain SNPs of TGF-β gene have an association with RAS pathogenesis. © 2017 Tehran University of Medical Sciences. All rights reserved. [ABSTRACT FROM AUTHOR]

Recurrent aphthous stomatitis (RAS) is known as the most common chronic disease of the oral cavity, which affects a range of 5-25% of the population. RAS appears to be associated with some human leukocyte antigen (HLA) class II alleles and haplotypes. This study attempts to survey the distribution of HLA-DRB and -DQB alleles among Iranian RAS patients and healthy controls. In order to evaluate the association of HLA-DR and DQ alleles and haplotypes, 54 patients with RAS and 100 unrelated healthy subjects as control group were investigated. Our data indicated that DRB1*13:17, DRB1*15:01, and DRB5*01 were significantly more frequent in RAS patients in comparison to controls. However, DRB3:01allele frequency was higher in the controls compared to the patients. The significantly frequent allele in the patients compared with the healthy subjects was HLA-DQB1*03:02. However, both HLA-DQB1*02:01 and HLA-DQB1*03:01 alleles were most frequent in the healthy individuals rather than the patients. The DRB*04/DQB1*03:01 and DRB*01:01/DQB1*02:01 haplotypes were significantly distributed in healthy subjects compared with patients. However, DRB*07:01/DQB1*03:02 haplotype was found to be significantly frequent in patients than controls. In respect of HLA genes, factors are involved in the incidence of RAS; various HLA-DRB and HLA-DQB1 alleles and the related haplotypes are suggested to be the three main RAS susceptibility factors in our population study. [ABSTRACT FROM AUTHOR]

Recurrent aphthous stomatitis (RAS) is a common oral inflammatory disease with unknown etiology in which the immune system seems to have a role in oral tolerance. Interleukin (IL)-10 is a cytokine synthesis inhibitory factor. Single nucleotide polymorphisms (SNPs) of IL10 gene could alter this cytokine production. The aim of this study was to investigate frequencies of IL10 alleles and genotypes in a group of individuals with RAS. Genomic DNA of 60 Iranian patients with RAS were typed for IL10 gene (C/A −1082, C/T −819, and C/A −592), using PCR-SSP method. Frequency of each allele and genotype was compared to control group. A significantly higher frequencies of the T allele at position −819 ( p = 0.006) and the A allele at position of −592 ( p < 0.001) were found in the patients with RAS group, when compared to the controls. IL10 GA genotype at position −1082 ( p = 0.007), CA genotype at position −592 ( p = 0.001), and CT genotype at position −819 ( p = 0.001) were significantly higher in the RAS patients. The results of this study suggest that certain SNPs of IL10 gene have association with predisposition of individuals to RAS. However, further multicenter studies should be conducted to confirm the results of this study. [ABSTRACT FROM AUTHOR]

Objective: Chronic urticaria is one of the most frequent cutaneous disorders. It is classified as chronic spontaneous and chronic inducible urticaria. Although mast cells are considered as the key cells that play the central role in the pathogenesis of chronic urticaria, other inflammatory cells including neutrophil, eosinophil and mononuclear cells along with T cells might also take part in the pathogenesis of chronic urticaria. The serum level of the inflammatory and anti-inflammatory cytokines such as IL-1β IL-4, IL-6, IL-13, TGF-β and TNF-α has been shown to be altered in the patients with chronic urticaria. In the current study, the IL-1α and IL-1β gene polymorphism was evaluated in patients with chronic urticaria comparing to the control group. Material and Methods: The study was designed as a matched case- control survey. IL-1α (in position -889 C>T) and IL-1β (in positions -511 and +3962 C>T) gene polymorphism was done by single specific primer-polymerase chain reaction (SSP- PCR) in a total of 90 patients with chronic spontaneous urticaria and 140 healthy controls. Autologous serum skin test (ASST) was done based on the universal guidelines. A thorough history was taken to confirm the diagnosis and rule out the inducible form of chronic urticaria. Results: Autoimmune chronic urticaria was found in 39 patients (43.8%) who showed positive ASST. At the position of -889 C>T in the IL-1α gene, C allele was the most frequent one. The frequency of TT genotype was the least, however TC and CC genotypes were found to have nearly the same frequency. At the -511 and +3962 C>T position in the gene of IL-1β, the most frequent allele in both group was C, however TC at -511 and CC at +3962 were the most frequent genotypes. No significant difference was found in the frequency of the alleles and genotypes in the polymorphic site of the IL-1α and IL-1β gene comparing to the controls (p>0.05). Conclusion: IL-1α and IL-1β gene polymorphism do not predispose patients to chronic spontaneous urticaria. [ABSTRACT FROM AUTHOR]

A letter to the editor in response to the article "Lack of Association between Interleukin-12 Gene Polymorphisms and Recurrent Aphthous Stomatitis," that was published in a previous issue of the journal is presented.

Transforming growth factor β (TGF-β) and interleukin 10 (IL-10) are two anti-inflammatory cytokines that are implicated in the pathogenesis of urticaria. The goal of this study was to examine the possible association of polymorphisms of TGF-β and IL-10 genes with susceptibility to chronic idiopathic urticaria (CIU). This study was conducted on 90 patients with CIU. Polymerase chain reaction (PCR) was done to determine the genotype at 5 polymorphic sites; TGF-β (codon10C/T and codon25G/C) and IL-10 (-1082G/A, -819C/T, and -592C/A). The C allele at codon 25 of TGF-β was more prevalent in CIU patients compared to controls (OR = 9.5, 95% CI = 5.4-16.8, P<0.001). Genotypes of CT and CG at 10 and 25 codons of TGF-β gene, respectively, and AG, CT, and CA for loci of -1082, -819, and -592 of IL-10 gene were significantly higher in CIU patients (P<0.001). In haplotype analysis, frequency of TGF-β haplotypes differed between patients with CIU and controls; CC haplotype was overrepresented, while CG and TG haplotypes were underrepresented (P<0.001). These results suggest that TGF-β and IL-10 genetic variability could contribute to susceptibility to CIU. Additionally, patients with CIU seem to have genotypes leading to high production of TGF-β and IL-10.