Berni Canani Roberto, Paparo Lorella, Nocerino Rita, Cosenza Linda, Pezzella Vincenza, Di Costanzo Margherita, Capasso Mario, Del Monaco Valentina, D'Argenio Valeria, Greco Luigi, Salvatore Francesco
Department of Translational Medical Science, University of Naples 'Federico II', Via S.Pansini, 5 80131 Naples, Italy ; European Laboratory for the Investigation of Food-Induced Diseases, University of Naples 'Federico II', Via S.Pansini, 5 80131 Naples, Italy ; CEINGE-Biotecnologie Avanzate s.c.ar.l, University of Naples 'Federico II', Via S.Pansini, 5 80131 Naples, Italy.
Department of Translational Medical Science, University of Naples 'Federico II', Via S.Pansini, 5 80131 Naples, Italy.
Clin Epigenetics. 2015 Mar 31;7(1):38. doi: 10.1186/s13148-015-0070-8. eCollection 2015.
Epigenetic changes in DNA methylation could regulate the expression of several allergy-related genes. We investigated whether tolerance acquisition in children with immunoglobulin E (IgE)-mediated cow's milk allergy (CMA) is characterized by a specific DNA methylation profile of Th2 (IL-4, IL-5) and Th1 (IL-10, IFN-γ)-associated cytokine genes.
DNA methylation of CpGs in the promoting regions of genes from peripheral blood mononuclear cells and serum level of IL-4, IL-5, IL-10 and INF-γ were assessed in children with active IgE-mediated CMA (group 1), in children who acquired tolerance to cow's milk proteins (group 2) and in healthy children (group 3). Forty children (24 boys, aged 3 to 18 months) were enrolled: 10 in group 1, 20 in group 2, and 10 in the control group. The DNA methylation profiles clearly separated active CMA patients from healthy controls. We observed an opposite pattern comparing subjects with active IgE-mediated CMA with healthy controls and group 2 children who outgrew CMA. The IL-4 and IL-5 DNA methylation was significantly lower, and IL-10 and INF-γ DNA methylation was higher in active IgE-mediated CMA patients. Gene promoter DNA methylation rates of all cytokines and respective serum levels were strongly correlated. Formula selection significantly influenced cytokine DNA methylation profiles in group 2.
Tolerance acquisition in children with IgE-mediated CMA is characterized by a distinct Th1 and Th2 cytokine gene DNA methylation pattern. These results suggest that DNA methylation may be a target for CMA prevention and treatment.
DNA甲基化的表观遗传变化可调节多个过敏相关基因的表达。我们研究了免疫球蛋白E(IgE)介导的牛奶过敏(CMA)儿童获得耐受是否以Th2(IL-4、IL-5)和Th1(IL-10、IFN-γ)相关细胞因子基因的特定DNA甲基化谱为特征。
评估了活动性IgE介导的CMA儿童(第1组)、获得牛奶蛋白耐受的儿童(第2组)和健康儿童(第3组)外周血单个核细胞基因启动子区域CpG的DNA甲基化以及IL-4、IL-5、IL-10和INF-γ的血清水平。共纳入40名儿童(24名男孩,年龄3至18个月):第1组10名,第2组20名,对照组10名。DNA甲基化谱清楚地将活动性CMA患者与健康对照区分开。与健康对照和已克服CMA的第2组儿童相比,活动性IgE介导的CMA受试者呈现相反的模式。活动性IgE介导的CMA患者中,IL-4和IL-5的DNA甲基化显著降低,而IL-10和INF-γ的DNA甲基化较高。所有细胞因子的基因启动子DNA甲基化率与各自的血清水平密切相关。配方选择对第2组细胞因子DNA甲基化谱有显著影响。
IgE介导的CMA儿童获得耐受的特征是Th1和Th2细胞因子基因有独特的DNA甲基化模式。这些结果表明DNA甲基化可能是CMA预防和治疗的靶点。