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母乳中的转化生长因子 β (TGFβ1) 与婴儿特应性的指标在出生队列中的关系。

Transforming growth factor beta (TGFβ1) in breast milk and indicators of infant atopy in a birth cohort.

机构信息

Department of Public Health Sciences, Henry Ford Hospital, Detroit, MI, USA; Center for Allergy, Asthma and Immunology Research, Henry Ford Hospital, Detroit, MI, USA.

出版信息

Pediatr Allergy Immunol. 2014 May;25(3):257-63. doi: 10.1111/pai.12205. Epub 2014 Feb 13.

Abstract

BACKGROUND

The infant gut's ability to suppress immunologic reactions to food proteins could be influenced by levels of TGFβ in breast milk. We hypothesized that lower levels of TGFβ(1) in the breast milk (BM) of mothers in the WHEALS birth cohort are associated with atopy at infant age 2-3 yrs.

METHODS

We used data collected during infancy in addition to the results of skin prick tests (SPT+) and measures of specific IgE >0.35 IU/ml (spIgE) to milk, egg, and peanut at infant age 2-3 years. Infants were classified as food allergic (FA) based on parental report of infant symptoms/diagnoses and information from clinical assessments.

RESULTS

Data for 304 cohort members were analyzed. Among non-black infants, BM-TGFβ(1) was lower for those classified as FA (vs. no FA) and those SPT+ (vs., SPT-), geometric mean = 1100 pg/ml vs. 1417pg/ml, p = 0.081; and 1100 pg/ml vs. 1415pg/ml, p = 0.064, respectively. Among infants of non-atopic mothers, BM-TGFβ(1) was lower for those with elevated (vs. not elevated) sIgE, geometric mean = 1347 pg/ml vs. 1651 pg/ml, p = 0.047. Using logistic regression, adjusted odds ratios describing the association of BM-TGFβ1 to the presence of atopic indicators in the infant were in the hypothesized direction only for non-black infants of non-atopic mothers: aORs for FA, sIgE and SPT+ were 0.08, 0.34, and 0.26 respectively; p = 0.091, 0.13, and 0.23.

CONCLUSION

Immune benefit of BM-TGFβ(1) could inform prevention strategies. Evidence of an association appears greatly influenced by infant race and maternal atopy. More research can determine if these relationships represent a modifiable risk factor for the development of food allergy in certain subgroups.

摘要

背景

婴儿肠道抑制食物蛋白免疫反应的能力可能受母乳中 TGFβ 水平的影响。我们假设 WHEALS 出生队列中母亲母乳中 TGFβ(1)水平较低与婴儿 2-3 岁时出现特应性有关。

方法

我们利用婴儿期收集的数据以及婴儿 2-3 岁时皮肤点刺试验(SPT+)和牛奶、鸡蛋和花生特异性 IgE >0.35 IU/ml(spIgE)的检测结果。根据父母报告的婴儿症状/诊断和临床评估信息,将婴儿分为食物过敏(FA)。

结果

对 304 名队列成员进行了数据分析。在非黑人婴儿中,FA 婴儿(vs. 无 FA 婴儿)和 SPT+婴儿(vs. SPT-婴儿)的母乳-TGFβ(1)水平较低,几何均数=1100pg/ml vs. 1417pg/ml,p=0.081;1100pg/ml vs. 1415pg/ml,p=0.064。在非特应性母亲的婴儿中,sIgE 升高(vs. 不升高)的婴儿母乳-TGFβ(1)水平较低,几何均数=1347pg/ml vs. 1651pg/ml,p=0.047。使用逻辑回归,调整后描述母乳-TGFβ1 与婴儿特应性指标存在的关联的比值比仅在非特应性非黑人母亲的婴儿中呈假设方向:FA、sIgE 和 SPT+的比值比分别为 0.08、0.34 和 0.26;p=0.091、0.13 和 0.23。

结论

母乳-TGFβ(1)的免疫益处可以为预防策略提供信息。关联的证据受婴儿种族和母亲特应性的极大影响。更多的研究可以确定这些关系是否代表某些亚组中食物过敏发展的可改变风险因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/104a/3997590/b9dc976d5b88/nihms561290f1.jpg

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