Department of Community Medicine and General Practice, Norwegian University of Science and Technology (NTNU), Trondheim, Norway.
Clin Exp Allergy. 2011 Nov;41(11):1545-54. doi: 10.1111/j.1365-2222.2011.03817.x. Epub 2011 Jul 13.
Intestinal microbiota undergoes substantial development during the first 2 years of life, important for intestinal immunologic development and maturation influencing systemic immune responses.
We aimed to investigate, using a prospective study design, whether allergen-specific IgE (sIgE) and atopic eczema are associated with variations in gut microbial colonization patterns in an unselected population during the first 2 years of life.
Faeces from 94 infants were repeatedly sampled from 10 days, 4 months, 1 and 2 years postnatal and analysed for 12 different bacterial species by quantitative real-time PCR. Venous blood samples from the infants were collected at 2 years of age and were analysed for sIgE for 12 specific allergens. The temporal gut colonization patterns for 42 sIgE-positive (sIgE≥0.35 kU/L) and 52 sIgE-negative children (sIgE<0.1 kU/L) were then compared. The association between colonization pattern and phenotype as atopic eczema according to UK Working Party (UKWP) criteria were also described.
Subjects with atopic sensitization had lower levels of Escherichia coli at 4 months and 1 year, higher levels of Bifidobacterium longum at 1 year and lower levels of Bacteroides fragilis at 2 years. For E. coli and B. longum, the differences were only transient and had disappeared by 2 years of age. For other species, there were no differences in colonization patterns, and we found no association between colonization pattern and atopic eczema.
We found temporal and transient variations in gut microbial colonization patterns associated with differences in sIgE sensitization at 2 years of age. A full understanding of the principles and mechanisms that underlie intestinal microbial colonization and diversity and host-microbiota relationships will be pivotal for the development of therapeutic approaches that manipulate the intestinal microbiota to maintain human health. [
ISRCTN28090297].
肠道微生物群在生命的头 2 年经历了显著的发展,这对肠道免疫发育和成熟以及影响全身免疫反应很重要。
我们旨在通过前瞻性研究设计,调查在生命的头 2 年内,未选择人群的过敏原特异性 IgE(sIgE)和特应性皮炎是否与肠道微生物定植模式的变化相关。
从 10 天、4 个月、1 岁和 2 岁的 94 名婴儿中反复采集粪便样本,并通过定量实时 PCR 分析 12 种不同的细菌种类。在 2 岁时采集婴儿的静脉血样,并分析 12 种特异性过敏原的 sIgE。然后比较 42 名 sIgE 阳性(sIgE≥0.35 kU/L)和 52 名 sIgE 阴性儿童(sIgE<0.1 kU/L)的肠道定植模式。还描述了根据英国工作组(UKWP)标准,定植模式与特应性皮炎表型(即特应性皮炎)的关联。
特应性致敏的受试者在 4 个月和 1 岁时的大肠杆菌水平较低,1 岁时双歧杆菌长双歧杆菌水平较高,2 岁时脆弱拟杆菌水平较低。对于大肠杆菌和长双歧杆菌,差异只是短暂的,到 2 岁时已经消失。对于其他物种,定植模式没有差异,我们没有发现定植模式与特应性皮炎之间的关联。
我们发现与 2 岁时 sIgE 致敏差异相关的肠道微生物定植模式存在时间和瞬时变化。全面了解肠道微生物定植和多样性以及宿主-微生物群关系的原理和机制,对于开发操纵肠道微生物群以维持人类健康的治疗方法至关重要。[注册号:ISRCTN28090297]。