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胃内给予转谷氨酰胺酶修饰的麦胶蛋白可干扰 DQ8 转基因小鼠对麦胶蛋白的全身和肠道免疫应答。

Intragastric administration of transamidated gliadin interferes with the systemic and intestinal immune responses to wheat gliadin in DQ8 transgenic mice.

机构信息

Institute of Food Sciences, CNR, via Roma 64, 83100 Avellino, Italy.

Institute of Food Sciences, CNR, via Roma 64, 83100 Avellino, Italy.

出版信息

Cytokine. 2024 Oct;182:156722. doi: 10.1016/j.cyto.2024.156722. Epub 2024 Aug 8.

DOI:10.1016/j.cyto.2024.156722
PMID:39116536
Abstract

We have previously shown the ability of transamidated gluten (spf) to modulate both innate and adaptive intestinal immunity elicited by wheat gliadin in HLA-DQ8 transgenic mice (DQ8 mice), a model of gluten sensitivity. Herein, we evaluated the influence of spf when administered intragastrically on the immune response to native gliadin in DQ8 mice. To address the issue, we analysed three regimens of antigen administration: before immunisation (pre-treatment), during immunisation (co-treatment) and through breast milk during the lactating phase (suckling treatment). Mice were immunised mucosally by intranasal delivery of digested wheat gliadin along with cholera toxin in multiple doses. After sacrifice, isolated spleen and mesenteric lymph node (MLN) cells were challenged in vitro and the cytokine profile of culture supernatants assessed by ELISA and multiparametric assay. We found that only pre-treatment with spf was effective in down-regulating the gliadin-specific IFN-γ response and only in spleen cells. Interestingly, spf pre-treatment also induced systemic IL-6, IL-17A and TNF-α. By contrast, we found that spf pre-treatment upregulated INF-γ in MLN but also significantly decreased IL-2. In conclusion, our data provide evidence that the preventive intragastric administration of transamidated gluten is able to interfere with the classical cytokine profile induced by gliadin via mucosal immunisation in a transgenic model expressing one of the HLA molecules associated with coeliac disease.

摘要

我们之前已经证明,转酰胺化面筋(spf)能够调节 HLA-DQ8 转基因小鼠(DQ8 小鼠)中由小麦醇溶蛋白引起的先天和适应性肠道免疫,这是一种乳糜泻敏感的模型。在此,我们评估了 spf 经胃内给药对 DQ8 小鼠天然醇溶蛋白免疫反应的影响。为了解决这个问题,我们分析了三种抗原给药方案:免疫前(预处理)、免疫期间(共同治疗)和哺乳期(哺乳治疗)。通过鼻内递送消化后的小麦醇溶蛋白和霍乱毒素多次对小鼠进行黏膜免疫。处死小鼠后,分离脾和肠系膜淋巴结(MLN)细胞进行体外挑战,并通过 ELISA 和多参数测定法评估培养上清液的细胞因子谱。我们发现,只有 spf 预处理才能有效下调醇溶蛋白特异性 IFN-γ 反应,且仅在脾细胞中。有趣的是,spf 预处理还诱导了全身 IL-6、IL-17A 和 TNF-α。相比之下,我们发现 spf 预处理增加了 MLN 中的 INF-γ,但也显著降低了 IL-2。总之,我们的数据提供了证据,表明经胃内预防性给予转酰胺化面筋能够通过在表达与乳糜泻相关的 HLA 分子之一的转基因模型中经黏膜免疫来干扰由醇溶蛋白引起的经典细胞因子谱。

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Intragastric administration of transamidated gliadin interferes with the systemic and intestinal immune responses to wheat gliadin in DQ8 transgenic mice.胃内给予转谷氨酰胺酶修饰的麦胶蛋白可干扰 DQ8 转基因小鼠对麦胶蛋白的全身和肠道免疫应答。
Cytokine. 2024 Oct;182:156722. doi: 10.1016/j.cyto.2024.156722. Epub 2024 Aug 8.
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