Department of Translational Medical Science, University Federico II, Naples, Italy.
CEINGE-Biotecnologie Avanzate s.c.ar.l., University Federico II, Naples, Italy.
Sci Rep. 2019 Feb 26;9(1):2828. doi: 10.1038/s41598-019-38738-w.
Epigenetic mechanisms could drive the disease course of cow's milk allergy (CMA) and formula choice could modulate these pathways. We compared the effect of two different dietary approaches on epigenetic mechanisms in CMA children. Randomized controlled trial on IgE-mediated CMA children receiving a 12-month treatment with extensively hydrolyzed casein formula containing the probiotic L.rhamnosus GG (EHCF + LGG) or with soy formula (SF). At the baseline, after 6 and 12 months of treatment FoxP3 methylation rate and its expression in CD4 T cells were assessed. At same study points IL-4, IL-5, IL-10, and IFN-γ methylation rate, expression and serum concentration, miRNAs expression were also investigated. 20 children (10/group) were evaluated. Baseline demographic, clinical and epigenetic features were similar in the two study groups. At 6 and 12 months, EHCF + LGG group showed a significant increase in FoxP3 demethylation rate compared to SF group. At the same study points, EHCF + LGG group presented a higher increase in IL-4 and IL-5 and a higher reduction in IL-10 and IFN-γ DNA methylation rate compared to SF group. A different modulation of miR-155, -146a, -128 and -193a expression was observed in EHCF + LGG vs. SF. Dietary intervention could exert a different epigenetic modulation on the immune system in CMA children.
表观遗传机制可能会影响牛奶过敏(CMA)的疾病进程,而配方的选择可以调节这些途径。我们比较了两种不同饮食方法对 CMA 儿童表观遗传机制的影响。这是一项针对 IgE 介导的 CMA 儿童的随机对照试验,他们接受了为期 12 个月的治疗,分别使用含有益生菌鼠李糖乳杆菌 GG(EHCF+LGG)的深度水解酪蛋白配方或大豆配方(SF)。在基线、治疗 6 个月和 12 个月时,评估 CD4 T 细胞中 FoxP3 甲基化率及其表达。在相同的研究点,还研究了 IL-4、IL-5、IL-10 和 IFN-γ 的甲基化率、表达和血清浓度以及 miRNA 的表达。共评估了 20 名儿童(每组 10 名)。两组研究对象的基线人口统计学、临床和表观遗传特征相似。在 6 个月和 12 个月时,EHCF+LGG 组的 FoxP3 去甲基化率与 SF 组相比显著增加。在相同的研究点,EHCF+LGG 组的 IL-4 和 IL-5 增加幅度更高,IL-10 和 IFN-γ 的 DNA 甲基化率降低幅度更高。与 SF 组相比,EHCF+LGG 组观察到 miR-155、-146a、-128 和 -193a 的表达有不同的调节。饮食干预可能会对 CMA 儿童的免疫系统产生不同的表观遗传调节作用。