Interleukin-33 gene expression and rs1342326 polymorphism in Behcet's disease

被引:11
作者
Talei, Mahsa [1 ,2 ]
Abdi, Ali [1 ,4 ,5 ]
Shanebandi, Dariush [2 ]
Jadidi-Niaragh, Farhad [2 ,5 ]
Khabazi, Alireza [1 ]
Babaie, Farhad [5 ,7 ]
Alipour, Shahriar [1 ]
Afkari, Babak [2 ,5 ]
Sakhinia, Ebrahim [1 ,6 ]
Babaloo, Zohreh [1 ,2 ,3 ,5 ]
机构
[1] Tabriz Univ Med Sci, Connect Tissue Res Ctr, Tabriz, Iran
[2] Tabriz Univ Med Sci, Immunol Res Ctr, Tabriz, Iran
[3] Tabriz Univ Med Sci, Drug Appl Res Ctr, Tabriz, Iran
[4] Tabriz Univ Med Sci, Student Res Comm, Tabriz, Iran
[5] Tabriz Univ Med Sci, Dept Immunol, Sch Med, Tabriz, Iran
[6] Tabriz Univ Med Sci, Dept Genet, Fac Med, Tabriz, Iran
[7] Urmia Univ Med Sci, Cellular & Mol Res Ctr, Orumiyeh, Iran
关键词
IL-33; Behcet; Disease; Gene polymorphism; VITAMIN-D; IL-33; ASSOCIATION; CYTOKINE; PATHOGENESIS; INSIGHTS; CHINESE; LEVEL; ST2;
D O I
10.1016/j.imlet.2018.11.005
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objective: Beheet's disease (BD) is a chronic multi-factorial inflammatory disease with the important role of genetic in activation of its inflammatory response. Interleukin (IL)-33 is a member of the IL-1 family of cytokines that affects innate and adaptive immune systems to promote inflammatory responses. In the current study, we investigated the association of IL-33 gene rs1342326 polymorphism and expression levels of this gene in peripheral blood mononuclear cells (PBMCs) with the susceptibility to BD in Azari population of Iran. Methods: We recruited 44 patients with BD and 61 age and sex-matched healthy controls in this cross-sectional study. The existence of rs1342326 T/G IL-33 gene single nucleotide polymorphism was investigated using Tetra Amplification Refractory Mutation System (Tetra-ARMS)-PCR. Allele and genotype distributions were evaluated among groups using chi-square or Fisher's test. Moreover, the mRNA levels of IL-33 in PBMCs were assessed through the Real-time PCR. Results: Patients with BD exhibited a significantly higher prevalence of the T/G genotype of rs1342326 polymorphism compared with the control group. Moreover, the expression level of IL-33 in PBMCs was significantly higher in the BD group compared to the healthy controls. Interestingly, the rs1342326 T/G polymorphism was associated with higher IL-33 expression in patients with BD. There was no association between the clinical manifestation of BD and disease activity with rs1342326 polymorphism and IL-33 expression. Conclusions: Our study implies that rs1342326 T/G polymorphism of the IL-33 gene may contribute to the genetic susceptibility to BD in part through regulation of the IL-33 expression.
引用
收藏
页码:120 / 124
页数:5
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