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剖宫产婴儿肠道微生物多样性减少、拟杆菌定植延迟和 Th1 反应减弱。

Decreased gut microbiota diversity, delayed Bacteroidetes colonisation and reduced Th1 responses in infants delivered by caesarean section.

机构信息

Department of Preparedness, Swedish Institute for Communicable Disease Control, , Solna, Sweden.

出版信息

Gut. 2014 Apr;63(4):559-66. doi: 10.1136/gutjnl-2012-303249. Epub 2013 Aug 7.

Abstract

OBJECTIVE

The early intestinal microbiota exerts important stimuli for immune development, and a reduced microbial exposure as well as caesarean section (CS) has been associated with the development of allergic disease. Here we address how microbiota development in infants is affected by mode of delivery, and relate differences in colonisation patterns to the maturation of a balanced Th1/Th2 immune response.

DESIGN

The postnatal intestinal colonisation pattern was investigated in 24 infants, born vaginally (15) or by CS (nine). The intestinal microbiota were characterised using pyrosequencing of 16S rRNA genes at 1 week and 1, 3, 6, 12 and 24 months after birth. Venous blood levels of Th1- and Th2-associated chemokines were measured at 6, 12 and 24 months.

RESULTS

Infants born through CS had lower total microbiota diversity during the first 2 years of life. CS delivered infants also had a lower abundance and diversity of the Bacteroidetes phylum and were less often colonised with the Bacteroidetes phylum. Infants born through CS had significantly lower levels of the Th1-associated chemokines CXCL10 and CXCL11 in blood.

CONCLUSIONS

CS was associated with a lower total microbial diversity, delayed colonisation of the Bacteroidetes phylum and reduced Th1 responses during the first 2 years of life.

摘要

目的

早期肠道微生物群对免疫发育具有重要的刺激作用,而微生物暴露减少以及剖宫产(CS)与过敏疾病的发展有关。在这里,我们探讨了婴儿的肠道微生物群如何受分娩方式的影响,并将定植模式的差异与平衡 Th1/Th2 免疫反应的成熟相关联。

设计

本研究在 24 名婴儿中调查了产后肠道定植模式,这些婴儿通过阴道(15 名)或 CS(9 名)分娩。在出生后 1 周、1、3、6、12 和 24 个月时,通过 16S rRNA 基因焦磷酸测序来描述肠道微生物群。在 6、12 和 24 个月时测量静脉血中 Th1 和 Th2 相关趋化因子的水平。

结果

CS 分娩的婴儿在生命的头 2 年中总微生物多样性较低。CS 分娩的婴儿还具有较低的拟杆菌门丰度和多样性,并且较少定植拟杆菌门。CS 分娩的婴儿血液中 Th1 相关趋化因子 CXCL10 和 CXCL11 的水平显著较低。

结论

CS 与总微生物多样性降低、拟杆菌门定植延迟以及生命头 2 年 Th1 反应减少有关。

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