益生菌在治疗和预防儿童过敏中的作用。

Bioscience and microflora Pub Date : 2011-01-01 Epub Date: 2011-11-17 DOI:10.12938/bifidus.30.119
Erkki Savilahti
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引用次数: 1

摘要

几项关于人类和实验动物过敏发病机制的研究继续表明,胃肠道中共生细菌在刺激和指导免疫系统方面的重要性。近年来,人们对用益生菌和益生菌调节共生菌群来预防和治疗食物过敏的兴趣成倍增加。我们最近研究了230名患有特应性皮炎和疑似牛奶过敏的婴儿。婴儿被随机分为三组,分别给予乳酸菌GG (LGG)、四种益生菌菌株混合(MIX)或安慰剂治疗4周。我们推测益生菌可诱导全身可检测的低度炎症,这可能解释了PBMC诱导的临床效果和细胞因子的分泌模式。为了研究益生菌预防儿童过敏的能力,我们招募了1223名携带过敏风险增加的胎儿的孕妇进行双盲安慰剂对照试验。母亲们从怀孕第36周开始使用四种益生菌的混合物或安慰剂。他们的婴儿连续6个月服用相同的益生菌和益生元半乳糖低聚糖。在2年的随访中,共有925名婴儿参与。过敏性疾病的累积发病率在合成菌组和安慰剂组之间没有显著差异。然而,合成抗生素能显著减少湿疹。合生剂对ige相关疾病的预防作用更为明显。在5年随访中,1018名有意治疗的婴儿中有891名(88%)参加了治疗。在益生菌组和安慰剂组中,过敏症状和与ige相关的过敏性疾病和致敏的频率相似,湿疹的频率在两组之间没有差异。特应性湿疹、变应性鼻炎和哮喘在各组中出现的频率相同。然而,在给予益生菌的剖腹产婴儿中,较少发生与ige相关的过敏性疾病。在剖腹产分娩的儿童中,我们注意到服用安慰剂的儿童双歧杆菌恢复的延迟上升,这是通过补充益生元和益生元来纠正的。对6个月大婴儿的粪便和血液的研究表明,益生菌可以增强肠道的炎症和免疫防御。益生菌治疗进一步刺激了免疫系统的成熟,因为给予益生菌的婴儿对呼吸道感染的抵抗力增强,疫苗抗体反应改善。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Probiotics in the treatment and prevention of allergies in children.

Probiotics in the treatment and prevention of allergies in children.

Probiotics in the treatment and prevention of allergies in children.

Probiotics in the treatment and prevention of allergies in children.

Several studies on the pathogenesis of allergy both in man and experimental animals continue to show the importance of commensal bacteria in the gastrointestinal tract in stimulating and directing the immune system. The interest in modulating commensal bacteria flora with pre- and probiotics to prevent and treat food allergy has multiplied in recent years. We recently studied 230 infants with atopic dermatitis and suspected cow's milk allergy. The infants were randomly allocated to groups which received Lactobacillus GG (LGG), a mixture of four probiotic strains (MIX) or placebo for 4 weeks. We inferred that probiotics induce systemically detectable low-grade inflammation, which may explain the clinical effects and the secretion pattern of cytokines induced by PBMC. To study the ability of probiotics to prevent allergy in children, we recruited 1223 pregnant women carrying fetuses at increased risk of allergy for a double-blind placebo-controlled trial. Mothers used a mixture of four probiotic bacteria or a placebo from the 36th week of gestation. Their infants received the same probiotics plus prebiotic galacto-oligosaccharides for 6 months. At the 2-year follow-up, a total of 925 infants participated. The cumulative incidence of allergic disease did not differ significantly between the synbiotic and the placebo group. However, synbiotics significantly reduced eczema. The preventive effect of synbiotics was more pronounced against IgE-associated diseases. At the 5 year follow-up, 891(88%) of the 1018 intention-to-treat infants attended. In the probiotic and placebo groups, frequencies of allergic symptoms and IgE-associated allergic disease and sensitization were similar, and the frequencies of eczema did not differ between the groups. Atopic eczema, allergic rhinitis and asthma appeared equal frequency in the groups. However, less IgE-associated allergic disease occurred in the cesarean-delivered infants given probiotics. In cesarean-delivered childen, we noticed a delayed rise in bifidobacteria recovery in placebo-treated children which was corrected by pro- and prebiotic supplementation. Indications from studies of feces and blood at the age 6 months suggest that probiotics may enhance both inflammation and immune defence of the gut. The probiotic treatment further stimulated maturation of the immune system since the infants given probiotics showed increased resistance to respiratory infections and improved vaccine antibody responses.

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