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在乳糜泻和相关的 1 型糖尿病患者的小肠黏膜中,紧密连接蛋白 1 基因的表达降低,FOXP3 表达增加。

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.

机构信息

Institute of General and Molecular Pathology, Department of Immunology, University of Tartu, Ravila 19, Tartu, Estonia.

出版信息

Int Arch Allergy Immunol. 2011;156(4):451-61. doi: 10.1159/000324456. Epub 2011 Aug 10.

Abstract

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 β-lactoglobulin, bovine α-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.

摘要

背景

已有研究报道,调节性 T 细胞(FOXP3 表达)在乳糜泻(CD)和 1 型糖尿病(T1D)发病机制中的作用。最近的数据特别关注肠道屏障与免疫调节过程之间的相互作用。我们旨在确定紧密连接蛋白 1(TJP1)的表达是否在 CD 和 T1D 中发生改变,TJP1 的表达反映了小肠黏膜通透性。

方法

通过实时 PCR 检测 14 例 CD 患儿、12 例 CD 合并 T1D 患儿和 40 例对照者小肠活检组织中 TJP1 和 FOXP3 基因的转录水平。通过 ELISA 法检测血清 IgA 和 IgG 对脱酰胺麦胶、牛β-乳球蛋白、牛α-酪蛋白和人组织转谷氨酰胺酶(tTG)的反应。

结果

FOXP3 mRNA 的表达水平在 CD 和 T1D 患儿中最高,明显高于 CD 患儿和对照组(p = 0.02)。相反,TJP1 mRNA 的表达水平在 CD 和 T1D 患儿中最低(p = 0.01)。CD 和 T1D 患儿血清中抗脱酰胺麦胶 IgA 和抗 tTG IgA 水平最高(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)水平呈高度相关。

结论

在 CD 患者,特别是在合并 T1D 的患者中,TJP1 表达的显著下降伴随着 FOXP3 表达的增加。这可能反映了试图维持免疫耐受,以平衡 CD 相关的 T1D 中小肠黏膜完整性的丧失。

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