Association between TH2 Cytokine Gene Polymorphisms and Risk of Bullous Pemphigoid

被引:18
|
作者
Tabatabaei-Panah, Pardis-Sadat [1 ]
Moravvej, Hamideh [2 ]
Alirajab, Marzieh [1 ]
Etaaty, Ahmad [1 ]
Geranmayeh, Maryam [1 ]
Hosseine, Farzaneh [1 ]
Khansari, Atousa [1 ]
Mahdian, Mohadeseh [1 ]
Mirhashemi, Mahsa [1 ]
Parvizi, Samira [1 ]
Sakhaie, Fatemeh [1 ]
Ludwig, Ralf J. [3 ]
Akbarzadeh, Reza [2 ,3 ,4 ]
机构
[1] Islamic Azad Univ, East Tehran Branch, Biol Dept, Tehran, Iran
[2] Shahid Beheshti Univ Med Sci, Skin Res Ctr, Tehran, Iran
[3] Univ Lubeck, Lubeck Inst Expt Dermatol, Lubeck, Germany
[4] Univ Lubeck, Inst Anat, D-23562 Lubeck, Germany
关键词
Bullous pemphigoid; autoimmune disease; Th2; cytokines; gene polymorphism; ATOPIC-DERMATITIS; BLISTER FLUID; IMMUNE DEVIATION; RECEPTOR GENE; SERUM; DISEASE; IL-13; INTERLEUKIN-4; EXPRESSION; IMPACT;
D O I
10.1080/08820139.2020.1832113
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: T-helper 2 (Th2)-associated cytokines are involved in the pathogenesis of bullous pemphigoid (BP), an autoimmune skin disease. Increased expression of Th2 cytokines such as interleukin-4 (IL-4), IL-5, IL-6, IL-10, and IL-13 have been observed in serum, skin biopsies and/or blister fluid. This study aimed to uncover a possible association between Th2 cytokine genetic variations and susceptibility to BP. Methods:In a cohort study, blood samples of BP patients and controls were obtained and variations in IL-4 (rs2243250 and rs2070874), IL-4R (rs1805010), IL-5 (rs2069812), IL-6 (rs1800795), IL-10 (rs1800896, rs1800871, and rs1800872), and IL-13 (rs1800925 and rs20541) were genotyped by PCR-RFLP assays. Furthermore, quantitative expression levels of IL-13 gene were evaluated by real-time RT-PCR analysis. Results:Among the studied variations, a significantly higher frequency of the C-allele was observed in IL-13 gene variation (rs1800925) in the healthy individuals than BP patients. This may indicate a protective effect of C-allele on predisposition to BP. Considering individuals carrying polymorphic genotypes compared to wild genotype, the minor G-allele of IL-4R rs1805010 and A-allele of IL-13 rs20541 had a promotive and protective effect, respectively, on predisposing to the development of BP. No significant difference in IL-13 mRNA expression was detected between BP patients and healthy individuals. Conclusions:Our results indicate that IL-13 rs1800925 variation may be a protective genetic marker for the development of BP. Given this preventive effect against BP, therapeutic strategies could potentially be developed interfering with the functions of IL-13 cytokine, which seems to be integral in the pathogenesis of eosinophilic inflammatory disorders, such as BP.
引用
收藏
页码:343 / 356
页数:14
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