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Influence of early gut microbiota on the maturation of childhood mucosal and systemic immune responses.

机译:早期肠道菌群对儿童粘膜和全身免疫反应成熟的影响。

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INTRODUCTION: Among sensitized infants, those with high, as compared with low levels, of salivary secretory IgA (SIgA) are less likely to develop allergic symptoms. Also, early colonization with certain gut microbiota, e.g. Lactobacilli and Bifidobacterium species, might be associated with less allergy development. Although animal and in vitro studies emphasize the role of the commensal gut microbiota in the development of the immune system, the influence of the gut microbiota on immune development in infants is unclear. OBJECTIVE: To assess whether early colonization with certain gut microbiota species associates with mucosal and systemic immune responses i.e. salivary SIgA and the spontaneous Toll-like receptor (TLR) 2 and TLR4 mRNA expression and lipopolysaccharide (LPS)-induced cytokine/chemokine responses in peripheral blood mononuclear cells (PBMCs). METHODS: Fecal samples were collected at 1 week, 1 month and 2 months after birth from 64 Swedish infants, followed prospectively up to 5 years of age. Bacterial DNA was analysed with real-time PCR using primers binding to Clostridium difficile, four species of bifidobacteria, two lactobacilli groups and Bacteroides fragilis. Saliva was collected at age 6 and 12 months and at 2 and 5 years and SIgA was measured with ELISA. The PBMCs, collected 12 months after birth, were analysed for TLR2 and TLR4 mRNA expression with real-time PCR. Further, the PBMCs were stimulated with LPS, and cytokine/chemokine responses were measured with Luminex. RESULTS: The number of Bifidobacterium species in the early fecal samples correlated significantly with the total levels of salivary SIgA at 6 months. Early colonization with Bifidobacterium species, lactobacilli groups or C. difficile did not influence TLR2 and TLR4 expression in PBMCs. However, PBMCs from infants colonized early with high amounts of Bacteroides fragilis expressed lower levels of TLR4 mRNA spontaneously. Furthermore, LPS-induced production of inflammatory cytokines and chemokines, e.g. IL-6 and CCL4 (MIP-1 beta), was inversely correlated to the relative amounts of Bacteroides fragilis in the early fecal samples. CONCLUSION: Bifidobacterial diversity may enhance the maturation of the mucosal SIgA system and early intense colonization with Bacteroides fragilis might down-regulate LPS responsiveness in infancy.
机译:简介:在致敏婴儿中,唾液分泌性IgA(SIgA)含量高而水平低的婴儿则不太可能出现过敏症状。同样,早期定植某些肠道菌群,例如乳酸杆菌和双歧杆菌可能与较少的过敏发展有关。尽管动物和体外研究强调了共生肠道菌群在免疫系统发育中的作用,但尚不清楚肠道菌群对婴儿免疫发育的影响。目的:评估某些肠道菌群物种的早期定殖是否与粘膜和全身免疫反应有关,即唾液SIgA和自发的Toll样受体(TLR)2和TLR4 mRNA表达以及脂多糖(LPS)诱导的外周细胞因子/趋化因子反应血液单核细胞(PBMC)。方法:在出生后1周,1个月和2个月时收集了64名瑞典婴儿的粪便样本,预期随访至5岁。使用结合艰难梭菌,四种双歧杆菌,两个乳杆菌组和脆弱拟杆菌的引物,通过实时PCR分析细菌DNA。在6、12个月,2和5岁时收集唾液,并通过ELISA测量SIgA。用实时PCR分析出生后12个月收集的PBMC的TLR2和TLR4 mRNA表达。此外,用LPS刺激PBMC,并用Luminex测量细胞因子/趋化因子反应。结果:早期粪便样品中双歧杆菌的数量与6个月时唾液SIgA的总水平显着相关。双歧杆菌,乳酸杆菌或艰难梭菌的早期定殖不会影响PBMC中TLR2和TLR4的表达。但是,早期定植在大量脆弱类拟杆菌中的婴儿的PBMC自发表达了较低水平的TLR4 mRNA。此外,LPS诱导的炎性细胞因子和趋化因子的产生,例如。 IL-6和CCL4(MIP-1 beta)与早期粪便样品中脆弱拟杆菌的相对含量成反比。结论:双歧杆菌的多样性可能会增强粘膜SIgA系统的成熟,而早期脆弱的拟杆菌的强烈定殖可能会下调婴儿期LPS的反应能力。

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