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糖巨肽治疗过敏的潜在新机制:肠道微生物群的变化、转化生长因子-β的上调以及肥大细胞的抑制。

Novel Mechanisms Underlying the Therapeutic Effect of Glycomacropeptide on Allergy: Change in Gut Microbiota, Upregulation of TGF-β, and Inhibition of Mast Cells.

作者信息

Jiménez Mariela, Cervantes-García Daniel, Muñoz Yualli Haydee, García Alejandra, Haro Luis Miguel, Salinas Eva

机构信息

Department of Microbiology, Basic Science Center, Autonomous University of Aguascalientes, Aguascalientes, Mexico.

出版信息

Int Arch Allergy Immunol. 2016;171(3-4):217-226. doi: 10.1159/000453035. Epub 2017 Jan 4.

Abstract

BACKGROUND

The prevalence of allergic diseases is globally increasing. We have previously described that glycomacropeptide (GMP), a bioactive milk peptide, has therapeutic value in experimental models of skin hypersensitivity, anaphylaxis, and asthma, as it prevents an excessive T helper type 2 cell immune response. The aim of this study was to analyze the effect of GMP on key elements directly involved in the development or control of allergy, in order to improve the precise knowledge about its mechanism of action.

METHODS

Rats were systemically sensitized with ovalbumin and orally treated with GMP. Levels of Lactobacillus, Bifidobacterium, and Bacteroides were analyzed in their feces. Splenocytes were isolated and the production of transforming growth factor (TGF)-β by allergens was measured. Intradermal skin reactions were developed to evaluate in vivo activation of mast cells. Peritoneal mast cells were isolated and activated by the allergen, and histamine secretion was determined.

RESULTS

GMP administration increased the amount of intestinal Lactobacillus and Bifidobacterium of allergen-sensitized animals after 3 days of treatment. The increase in Bacteroides was also significant, but only after 17 days of GMP administration. Ten days after treatment cessation, Lactobacillus and Bacteroides were still elevated. GMP intake also elevated the production of TGF-β in the splenocytes of sensitized animals. In addition, treatment with GMP attenuated mast cell activation by the allergen and inhibited histamine secretion, without affecting the number of mast cells.

CONCLUSIONS

The prebiotic action of GMP on allergy-protective microbiota, an increase in TGF-β production, and a reduction in mast cell response to allergens are novel mechanisms that explain the antiallergic activity of GMP.

摘要

背景

过敏性疾病的患病率在全球范围内呈上升趋势。我们之前曾描述过,糖巨肽(GMP)是一种具有生物活性的乳肽,在皮肤过敏、过敏反应和哮喘的实验模型中具有治疗价值,因为它能预防过度的2型辅助性T细胞免疫反应。本研究的目的是分析GMP对直接参与过敏发生或控制的关键因素的影响,以更准确地了解其作用机制。

方法

用卵清蛋白对大鼠进行全身致敏,并对其口服GMP进行治疗。分析其粪便中乳酸杆菌、双歧杆菌和拟杆菌的水平。分离脾细胞并检测变应原诱导的转化生长因子(TGF)-β的产生。通过皮内皮肤反应评估肥大细胞的体内活化情况。分离腹膜肥大细胞并用变应原进行活化,然后测定组胺分泌量。

结果

治疗3天后,给予GMP可增加致敏动物肠道中乳酸杆菌和双歧杆菌的数量。给予GMP 17天后,拟杆菌数量的增加也很显著。停止治疗10天后,乳酸杆菌和拟杆菌数量仍保持升高。摄入GMP还可提高致敏动物脾细胞中TGF-β的产生。此外,GMP治疗可减轻变应原对肥大细胞的活化作用并抑制组胺分泌,但不影响肥大细胞的数量。

结论

GMP对具有过敏保护作用的微生物群的益生元作用、TGF-β产生的增加以及肥大细胞对变应原反应的降低是解释GMP抗过敏活性的新机制。

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