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Lower expression of tight junction protein 1 gene and increased FOXP3 expression in the small bowel mucosa in coeliac disease and associated type 1 diabetes mellitus.

机译:乳糜泻和相关的1型糖尿病的小肠粘膜中紧密连接蛋白1基因的表达降低,而FOXP3表达升高。

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BACKGROUND: The role of regulatory T cells expressing FOXP3 in the pathogenesis of coeliac disease (CD) and type 1 diabetes (T1D) has been reported. Recent data have placed special focus on the interplay between the intestinal barrier and immunoregulatory processes. We aimed to determine whether the expression of tight junction protein 1 (TJP1), which reflects small bowel mucosa permeability, is changed in CD and T1D. METHODS: Transcription levels of TJP1 and FOXP3 genes were evaluated in the small bowel biopsies of 14 children with CD, 12 with CD and coexisting T1D and 40 controls using real-time PCR. Serum IgA and IgG to deamidated gliadin, bovine beta-lactoglobulin, bovine alpha-casein and human tissue transglutaminase (tTG) were determined by ELISA. RESULTS: The highest expression of FOXP3 mRNA was seen in patients with CD and T1D compared to patients with CD alone and controls (p = 0.02). In contrast, the lowest level of TJP1 mRNA expression was found in patients with CD and T1D (p = 0.01). The levels of IgA to deamidated gliadin and tTG were highest in patients with CD and T1D (p = 0.0001 and 0.01, respectively). The expression of FOXP3 mRNA correlated highly with the level of anti-gliadin IgA (p = 0.02) and anti-tTG IgA antibodies (p = 0.004). CONCLUSION: The significant decline in TJP1 expression in CD patients, particularly in those with coexisting T1D, was accompanied by an increase in FOXP3 expression. This might reflect an attempt to maintain immune tolerance to counterbalance the loss of mucosal integrity in the small intestine in CD associated with T1D.
机译:背景:已经报道了表达FOXP3的调节性T细胞在乳糜泻(CD)和1型糖尿病(T1D)发病中的作用。最近的数据特别关注肠屏障和免疫调节过程之间的相互作用。我们的目的是确定CD和T1D中反映小肠粘膜通透性的紧密连接蛋白1(TJP1)的表达是否改变。方法:实时荧光定量PCR检测14例CD患儿,12例CD患儿和共存的T1D患儿的小肠活检组织中TJP1和FOXP3基因的转录水平。通过ELISA测定了去酰胺化的麦醇溶蛋白,牛β-乳球蛋白,牛α-酪蛋白和人组织转谷氨酰胺酶(tTG)的血清IgA和IgG。结果:与单独的CD患者和对照组相比,CD和T1D患者中FOXP3 mRNA的表达最高(p = 0.02)。相反,CD和T1D患者的TJP1 mRNA表达最低(p = 0.01)。 CD和T1D患者的脱酰胺化麦醇溶蛋白和tTG的IgA水平最高(分别为p = 0.0001和0.01)。 FOXP3 mRNA的表达与抗麦胶蛋白IgA(p = 0.02)和抗tTG IgA抗体(p = 0.004)高度相关。结论:CD患者中TJP1表达的显着下降,尤其是与T1D共存的患者,伴随着FOXP3表达的增加。这可能反映了维持免疫耐受以平衡与T1D相关的CD小肠粘膜完整性损失的尝试。

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