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Importance of intestinal colonisation in the maturation ofhumoral immunity in early infancy: a prospective follow up study ofhealthy infants aged 0-6 months

机译:小肠定植在成熟中的重要性婴儿早期的体液免疫:一项前瞻性随访研究0-6个月的健康婴儿

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摘要

AIM—To evaluate the role of intestinal microflora and early formula feeding in the maturation of humoral immunity in healthy newborn infants.
STUDY DESIGN—Sixty four healthy infants were studied. Faecal colonisation with Bacteroides fragilis group, Bifidobacterium-like, and Lactobacillus-like bacteria was examined at 1, 2, and 6 months of age, and also the number of IgA-secreting, IgM-secreting, and IgG-secreting cells (detected by ELISPOT) at 0, 2, and 6 months of age.
RESULTS—Intestinal colonisation with bacteria from the B fragilis group was more closely associated with maturation of IgA-secreting and IgM-secreting cells than colonisation with the other bacterial genera studied or diet. Infants colonised with B fragilis at 1month of age had more IgA-secreting and IgM-secreting cells/106 mononuclear cells at 2 months of age (geometric mean (95% confidence interval) 1393 (962 to 2018) and 754 (427 to 1332) respectively) than infants not colonised (1015 (826 to 1247) and 394 (304 to 511) respectively); p = 0.04 andp = 0.009 respectively.
CONCLUSIONS—The typeof bacteria colonising the intestine of newborns and the timing maydetermine the immunomodulation of the naive immune system.

机译:目的—评估肠道菌群和早期配方食品喂养对健康新生儿体液免疫成熟的作用。
研究设计—研究了64例健康婴儿。在1、2和6个月大时检查了脆弱的拟杆菌,类双歧杆菌和类乳杆菌的粪便定植,以及分泌IgA,分泌IgM和IgG的细胞数量(通过ELISPOT)分别在0、2和6个月大。
结果-脆弱的B组细菌在肠道中的定殖与分泌IgA和IgM的细胞的成熟更紧密相关,而不是与其他细菌属定殖研究或饮食。 1个月大时以脆弱的B菌定殖的婴儿在2个月大时具有更多的IgA分泌和IgM分泌细胞/ 10 6 单核细胞(几何平均值(95%置信区间))1393(962至2018 )和754(分别为427至1332)和没有定居的婴儿(分别为1015(826至1247)和394(304至511))。 p = 0.04和p分别为0.009。
结论—类型细菌定居新生儿肠道的时间确定原始免疫系统的免疫调节。

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