Bantz Selene K, Zhu Zhou, Zheng Tao
Section of Allergy and Clinical Immunology, Yale University, School of Medicine, New Haven, 06520, USA.
J Clin Cell Immunol. 2014 Apr;5(2). doi: 10.4172/2155-9899.1000202.
The development of atopic dermatitis (AD) in infancy and subsequent allergic rhinitis and asthma in later childhood is known as the atopic march. This progressive atopy is dependent on various underlying factors such as the presence of filaggrin mutations as well as the time of onset and severity of AD. Clinical manifestations vary among individuals. Previously it was thought that atopic disorders may be unrelated with sequential development. Recent studies support the idea of a causal link between AD and later onset atopic disorders. These studies suggest that a dysfunctional skin barrier serves as a site for allergic sensitization to antigens and colonization of bacterial super antigens. This induces systemic Th2 immunity that predisposes patients to allergic nasal responses and promotes airway hyper reactivity. While AD often starts early in life and is a chronic condition, new research signifies that there may be an optimal window of time in which targeting the skin barrier with therapeutic interventions may prevent subsequent atopic disorders. In this review we highlight recent studies describing factors important in the development of atopic disorders and new insights in our understanding of the pathogenesis of the atopic march.
婴儿期特应性皮炎(AD)的发生以及随后儿童期后期的过敏性鼻炎和哮喘被称为特应性进程。这种渐进性特应性取决于多种潜在因素,如丝聚合蛋白突变的存在以及AD的发病时间和严重程度。个体的临床表现各不相同。以前认为特应性疾病可能与顺序发展无关。最近的研究支持AD与后期发生的特应性疾病之间存在因果联系的观点。这些研究表明,功能失调的皮肤屏障是对抗原过敏致敏和细菌超抗原定植的部位。这会诱导全身性Th2免疫,使患者易发生过敏性鼻反应并促进气道高反应性。虽然AD通常在生命早期开始且是一种慢性疾病,但新的研究表明,可能存在一个最佳时间窗,在此期间通过治疗干预针对皮肤屏障可能预防随后的特应性疾病。在本综述中,我们重点介绍了描述特应性疾病发展中重要因素的最新研究以及我们对特应性进程发病机制理解的新见解。