Primary Atopic Disorders

被引:50
作者
Milner, Joshua D. [1 ]
机构
[1] Columbia Univ, Irving Med Ctr, Dept Pediat, New York, NY 10032 USA
来源
ANNUAL REVIEW OF IMMUNOLOGY, VOL 38 | 2020年 / 38卷
关键词
allergy; genetics; primary atopic disorders; monogenic; Th2; mast cell function; skin barrier; ALDRICH-SYNDROME PROTEIN; OF-FUNCTION MUTATIONS; HYPER-IGE SYNDROME; REGULATORY T-CELLS; SYSTEMIC LUPUS-ERYTHEMATOSUS; SKIN BARRIER FUNCTION; COMBINED IMMUNODEFICIENCY; PROLIDASE DEFICIENCY; HYPERIMMUNOGLOBULINEMIA-E; IMMUNE DYSREGULATION;
D O I
10.1146/annurev-immunol-042718-041553
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Primary atopic disorders describes a series of monogenic diseases that have allergy- or atopic effector-related symptoms as a substantial feature. The underlying pathogenic genetic lesions help illustrate fundamental pathways in atopy, opening up diagnostic and therapeutic options for further study in those patients, but ultimately for common allergic diseases as well. Key pathways affected in these disorders include T cell receptor and B cell receptor signaling, cytokine signaling, skin barrier function, and mast cell function, as well as pathways that have not yet been elucidated. While comorbidities such as classically syndromic presentation or immune deficiency are often present, in some cases allergy alone is the presenting symptom, suggesting that commonly encountered allergic diseases exist on a spectrum of monogenic and complex genetic etiologies that are impacted by environmental risk factors.
引用
收藏
页码:785 / 808
页数:24
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