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早期生活前体、表观遗传学与食物过敏的发生发展。

Early life precursors, epigenetics, and the development of food allergy.

机构信息

Center on the Early Life Origins of Disease, Department of Population, Family and Reproductive Health, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, MD 21205-2179, USA.

出版信息

Semin Immunopathol. 2012 Sep;34(5):655-69. doi: 10.1007/s00281-012-0323-y. Epub 2012 Jul 10.

Abstract

Food allergy (FA), a major clinical and public health concern worldwide, is caused by a complex interplay of environmental exposures, genetic variants, gene-environment interactions, and epigenetic alterations. This review summarizes recent advances surrounding these key factors, with a particular focus on the potential role of epigenetics in the development of FA. Epidemiologic studies have reported a number of nongenetic factors that may influence the risk of FA, such as timing of food introduction and feeding pattern, diet/nutrition, exposure to environmental tobacco smoking, prematurity and low birth weight, microbial exposure, and race/ethnicity. Current studies on the genetics of FA are mainly conducted using candidate gene approaches, which have linked more than 10 genes to the genetic susceptibility of FA. Studies on gene-environment interactions of FA are very limited. Epigenetic alteration has been proposed as one of the mechanisms to mediate the influence of early life environmental exposures and gene-environment interactions on the development of diseases later in life. The role of epigenetics in the regulation of the immune system and the epigenetic effects of some FA-associated environmental exposures are discussed in this review. There is a particular lack of large-scale prospective birth cohort studies that simultaneously assess the interrelationships of early life exposures, genetic susceptibility, epigenomic alterations, and the development of FA. The identification of these key factors and their independent and joint contributions to FA will allow us to gain important insight into the biological mechanisms by which environmental exposures and genetic susceptibility affect the risk of FA and will provide essential information to develop more effective new paradigms in the diagnosis, prevention, and management of FA.

摘要

食物过敏(FA)是一个全球性的主要临床和公共卫生问题,由环境暴露、遗传变异、基因-环境相互作用和表观遗传改变等多种因素的复杂相互作用引起。本综述总结了这些关键因素的最新进展,特别关注了表观遗传在 FA 发生发展中的潜在作用。流行病学研究报告了许多非遗传因素可能影响 FA 的风险,例如食物引入和喂养模式的时间、饮食/营养、暴露于环境烟草烟雾、早产和低出生体重、微生物暴露和种族/民族。目前关于 FA 遗传学的研究主要采用候选基因方法进行,该方法已将 10 多个基因与 FA 的遗传易感性联系起来。FA 的基因-环境相互作用研究非常有限。表观遗传改变被提出作为介导早期生活环境暴露和基因-环境相互作用对生命后期疾病发展影响的机制之一。本综述讨论了表观遗传在免疫系统调节中的作用以及一些与 FA 相关的环境暴露的表观遗传效应。特别缺乏同时评估生命早期暴露、遗传易感性、表观遗传改变与 FA 发生发展之间相互关系的大规模前瞻性出生队列研究。确定这些关键因素及其对 FA 的独立和联合贡献,将使我们能够深入了解环境暴露和遗传易感性影响 FA 风险的生物学机制,并为 FA 的诊断、预防和管理提供新的有效范式提供重要信息。

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