Division of Infection, Inflammation and Immunity, School of Medicine, University of Southampton, Southampton, United Kingdom.
J Allergy Clin Immunol. 2010 Feb;125(2 Suppl 2):S81-94. doi: 10.1016/j.jaci.2009.10.071.
Allergic diseases are complex genetic diseases resulting from the effect of multiple genetic and interacting environmental factors on their pathophysiology. Recent years have seen considerable progress in unraveling the contribution of these factors to an individual subject's susceptibility to, subsequent development of, and severity of disease. This has resulted in increasing insight into novel areas of allergic disease pathophysiology, for example the significant role played by locally acting tissue susceptibility factors like epithelial/epidermal barrier function and remodeling, such as filaggrin, ADAM33, and GSDML/ORMDL3, in patients with atopic dermatitis and asthma. Furthermore, studies of gene-environment interactions and Mendelian randomization approaches have led to increased insight into the importance of environmental triggers for allergic disease. Studies of the timing of action of genetic variants in determining disease susceptibility have highlighted the importance of in utero development and early life in determining susceptibility to allergic disease. In the future, genetic discoveries in allergic disease will potentially lead to better endophenotyping, prognostication, prediction of treatment response, and insights into molecular pathways to develop more targeted therapy for these conditions.
过敏疾病是复杂的遗传疾病,由多种遗传和相互作用的环境因素对其病理生理学的影响导致。近年来,在揭示这些因素对个体易感性、随后疾病的发展和严重程度的贡献方面取得了相当大的进展。这导致人们对过敏疾病病理生理学的新领域有了更多的了解,例如局部作用的组织易感性因素(如上皮/表皮屏障功能和重塑),如丝聚蛋白、ADAM33 和 GSDML/ORMDL3,在特应性皮炎和哮喘患者中的重要作用。此外,对基因-环境相互作用和孟德尔随机化方法的研究增加了对环境触发因素在过敏疾病中的重要性的了解。对决定疾病易感性的遗传变异作用时间的研究强调了在子宫内发育和生命早期对确定过敏疾病易感性的重要性。在未来,过敏疾病的遗传发现可能会导致更好的内表型、预后、治疗反应预测,并深入了解分子途径,为这些疾病开发更有针对性的治疗方法。