Thomas Sarah A, Lajoie Stephane
W. Harry Feinstone Department of Molecular Microbiology and Immunology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.
Department of Otolaryngology-Head and Neck Surgery, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
J Clin Invest. 2025 May 1;135(9). doi: 10.1172/JCI188352.
Type 2 (Th2) allergic diseases are chronic conditions characterized by a Th2-polarized immune response to allergens. These diseases can be categorized by affected barrier sites: skin (atopic dermatitis, allergic contact dermatitis), gut (food allergy), and respiratory tract (e.g., asthma, chronic rhinosinusitis). The global prevalence of Th2 allergic diseases has increased the need for a deeper understanding of their pathophysiology. Several associations have been identified between genetic variants in the genes encoding components of the complement system and allergic disease. Moreover, levels of several complement proteins are elevated in patients with allergy. Experimental evidence demonstrates that the complement system plays a critical role in the development of these diseases across barrier sites. While site-specific differences exist in the complement components involved, key pathways, particularly C3 and C5, are prominent across the skin, gut, and lung.
2型(Th2)过敏性疾病是一种慢性疾病,其特征是对过敏原产生Th2极化的免疫反应。这些疾病可根据受影响的屏障部位进行分类:皮肤(特应性皮炎、过敏性接触性皮炎)、肠道(食物过敏)和呼吸道(如哮喘、慢性鼻-鼻窦炎)。全球Th2过敏性疾病患病率的上升增加了深入了解其病理生理学的必要性。已经确定了补体系统成分编码基因中的遗传变异与过敏性疾病之间的几种关联。此外,过敏患者体内几种补体蛋白的水平升高。实验证据表明,补体系统在这些跨屏障部位疾病的发展中起关键作用。虽然所涉及的补体成分存在部位特异性差异,但关键途径,特别是C3和C5,在皮肤、肠道和肺部都很突出。