母体补充益生菌预防特应性皮炎后后代的全身炎症蛋白。

Q2 Medicine
Dinastry Pramadita Zakiudin, Anne Dorthea Bjerkenes Rø, Vibeke Videm, Torbjørn Øien, Melanie Rae Simpson
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引用次数: 0

摘要

背景:母亲补充益生菌对预防婴儿特应性皮炎(AD)有很好的效果。在一项名为“益生菌预防特隆赫姆儿童过敏”(proact)的随机对照研究中,母亲服用益生菌可使子女2岁时AD的累积发病率降低40%。然而,我们对益生菌如何预防AD的了解仍然有限,并且母体补充益生菌后炎症蛋白在婴儿中的作用尚不清楚。我们假设母体益生菌降低了2岁儿童的促炎蛋白,增加了抗炎蛋白,这是一种预防AD的机制。我们的目的是探索这一假设,以及这些蛋白与AD的存在、AD的严重程度以及益生菌的预防作用程度之间的关系。方法:在proact研究期间收集2岁儿童(n = 202)的血浆样本,proact是一项随机安慰剂对照试验,用于母体益生菌补充。这些样本使用多重接近延伸法分析了92种炎症蛋白。炎症蛋白与AD的存在和严重程度之间的关联,以及预防效果的程度,分别使用回归分析和无监督聚类分析进行估计。结果:组间观察到若干蛋白存在差异。益生菌组的CCL11和IL-17C较低,而AD患儿的IL-17C、MCP-4、uPA和CD6较高。细胞因子CCL20和IL-18与AD的严重程度有中度相关性(r = 0.35和r = 0.46)。聚类分析显示,在免疫检查点受体和炎症抑制酶含量最高的样本群中,益生菌对AD的预防作用最大。结论:与母体益生菌补充和AD存在及其严重程度相关的蛋白质值得关注,因为它们具有潜在的生物学相关性。当考虑哪些亚群从益生菌补充中受益时,聚类分析可能提供新的见解。需要更大规模的研究来证实这一结果。试验注册号:该研究于2005年9月12日在ClinicalTrials.gov (NCT00159523)上回顾性注册。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Systemic inflammatory proteins in offspring following maternal probiotic supplementation for atopic dermatitis prevention.

Systemic inflammatory proteins in offspring following maternal probiotic supplementation for atopic dermatitis prevention.

Systemic inflammatory proteins in offspring following maternal probiotic supplementation for atopic dermatitis prevention.

Background: Maternal probiotic supplementation has a promising effect on atopic dermatitis (AD) prevention in infancy. In the randomised controlled study, Probiotics in the Prevention of Allergy among Children in Trondheim (ProPACT), maternal probiotics reduced the cumulative incidence of AD in their offspring by 40% at 2 years of age. However, our understanding on how probiotics prevented AD is still limited, and the role of inflammatory proteins in infants following maternal probiotic supplementation is unclear. We hypothesised that maternal probiotics lowered pro-inflammatory proteins and increased anti-inflammatory proteins in their 2-year-old children as a mechanism of AD prevention. We aimed to explore this hypothesis and the association between these proteins and the presence of AD, severity of AD, and the degree of preventive effect of probiotics.

Methods: Plasma samples were collected from 2-year-old children (n = 202) during the ProPACT study, a randomised placebo-controlled trial of maternal probiotic supplementation. These samples were analysed for 92 inflammatory proteins using a multiplex proximity extension assay. Associations between inflammatory proteins and the presence and severity of AD, and the degree of preventive effect, was estimated individually using regression analysis and then collectively using unsupervised cluster analysis.

Results: Several proteins were observed to differ between the groups. The probiotic group had lower CCL11 and IL-17C, while children with AD had higher IL-17C, MCP-4, uPA, and CD6. Cytokine CCL20 and IL-18 had moderate correlation (r = 0.35 and r = 0.46) with the severity of AD. The cluster analysis revealed that children in the cluster of samples with the highest value of immune checkpoint receptors and inflammatory suppressor enzymes showed the greatest AD preventive effect from probiotics.

Conclusions: The proteins associated with both maternal probiotic supplementation and the presence and severity of AD warrant attention because of their potential biological relevance. Cluster analysis may provide a new insight when considering which subgroups benefit from probiotic supplementation. Larger studies are needed to confirm the results.

Trial registration number: The study was retrospectively registered at ClinicalTrials.gov (NCT00159523) on 12nd September 2005.

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来源期刊
Clinical and Molecular Allergy
Clinical and Molecular Allergy Medicine-Immunology and Allergy
CiteScore
8.20
自引率
0.00%
发文量
11
审稿时长
13 weeks
期刊介绍: Clinical and Molecular Allergy is an open access, peer-reviewed, online journal that publishes research on human allergic and immunodeficient disease (immune deficiency not related to HIV infection/AIDS). The scope of the journal encompasses all aspects of the clinical, genetic, molecular and inflammatory aspects of allergic-respiratory (Type 1 hypersensitivity) and non-AIDS immunodeficiency disorders. However, studies of allergic/hypersensitive aspects of HIV infection/AIDS or drug desensitization protocols in AIDS are acceptable. At the basic science level, this includes original work and reviews on the genetic and molecular mechanisms underlying the inflammatory response.
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