Institute of Molecular Cancer Research, University of Zürich, Zürich, Switzerland.
Department Experimental Immunology, Helmholtz Center for Infection Research, Braunschweig, Germany.
Clin Exp Allergy. 2017 Oct;47(10):1331-1341. doi: 10.1111/cea.12996. Epub 2017 Sep 11.
Food allergy is an increasingly common health problem in Western populations. Epidemiological studies have suggested both positive and negative associations between food allergy and infection with the gastric bacterium Helicobacter pylori.
The objective of this work was to investigate whether experimental infection with H. pylori, or prophylactic treatment with H. pylori-derived immunomodulatory molecules, affects the onset and severity of food allergy, either positively or negatively.
We infected neonatal C57BL/6 or C3H mice with H. pylori or treated animals with H. pylori components (bacterial lysate or the immunomodulator VacA) and subsequently subjected them to four different protocols for food allergy induction, using either ovalbumin or peanut extract as allergens for sensitization and challenge. Readouts included anaphylaxis scoring, quantification of allergen-specific serum IgE and IgG1 and of the mast cell protease MCPT1, as well as splenic T-helper-2 cell-derived cytokine production. Mesenteric lymph node CD4 FoxP3 regulatory T cells were subjected to flow cytometric quantification and sorting followed by qRT-PCR, and to DNA methylation analyses of the Treg-specific demethylated region (TSDR) within the FOXP3 locus.
Mice that had been infected with H. pylori or treated with H. pylori-derived immunomodulators showed reduced anaphylaxis upon allergen sensitization and challenge, irrespective of the allergen used. Most of the immunologic assays confirmed a protective effect of H. pylori. CD4 FoxP3 T cells were more abundant in protected mice and exhibited a stable Treg phenotype characterized by FOXP3 TSDR demethylation.
Helicobacter pylori confers protection against the anaphylaxis associated with ovalbumin and peanut allergy and affects the epigenome of T cells, thereby promoting stable Treg differentiation and functionality. Prophylactic treatment with H. pylori-derived immunomodulators appears to be a promising strategy for food allergy prevention.
食物过敏是西方人群中日益常见的健康问题。流行病学研究表明,食物过敏与胃幽门螺杆菌(Helicobacter pylori)感染之间存在正相关和负相关关系。
本研究旨在探讨幽门螺杆菌的实验感染或幽门螺杆菌衍生的免疫调节分子的预防性治疗是否会对食物过敏的发生和严重程度产生积极或消极的影响。
我们用幽门螺杆菌感染新生 C57BL/6 或 C3H 小鼠,或用幽门螺杆菌成分(细菌裂解物或免疫调节剂 VacA)治疗动物,然后用卵清蛋白或花生提取物作为过敏原进行 4 种不同的食物过敏诱导方案,检测指标包括过敏反应评分、过敏原特异性血清 IgE 和 IgG1 以及肥大细胞蛋白酶 MCPT1 的定量,以及脾辅助性 T 细胞(Th2)衍生细胞因子的产生。肠系膜淋巴结 CD4 FoxP3 调节性 T 细胞进行流式细胞术定量和分选,然后进行 qRT-PCR,并对 FOXP3 基因座中 Treg 特异性去甲基化区(TSDR)进行 DNA 甲基化分析。
无论使用哪种过敏原,感染幽门螺杆菌或用幽门螺杆菌衍生的免疫调节剂治疗的小鼠在过敏原致敏和挑战时过敏反应减轻。大多数免疫测定证实了幽门螺杆菌的保护作用。受保护的小鼠中 CD4 FoxP3 T 细胞更为丰富,表现出稳定的 Treg 表型,其特征为 FOXP3 TSDR 去甲基化。
幽门螺杆菌可预防卵清蛋白和花生过敏相关的过敏反应,并影响 T 细胞的表观基因组,从而促进稳定的 Treg 分化和功能。用幽门螺杆菌衍生的免疫调节剂进行预防性治疗似乎是预防食物过敏的一种有前途的策略。