Innate immunity, allergy and atopic dermatitis

被引:47
作者
Niebuhr, Margarete [1 ]
Werfel, Thomas [1 ]
机构
[1] Hannover Med Sch, Div Immunodermatol & Allergy Res, Dept Dermatol & Allergy, D-30449 Hannover, Germany
关键词
antimicrobial peptides; atopic dermatitis; epithelial barrier defect; filaggrin; innate immunity; TOLL-LIKE RECEPTOR-2; PLASMACYTOID DENDRITIC CELLS; STAPHYLOCOCCUS-AUREUS; BACTERIAL LIPOPROTEINS; FILAGGRIN MUTATIONS; RISK-FACTORS; ALPHA-TOXIN; SKIN; ECZEMA; POLYMORPHISM;
D O I
10.1097/ACI.0b013e32833e3163
中图分类号
R392 [医学免疫学];
学科分类号
100108 [医学免疫学];
摘要
Purpose of review We review here the recent discoveries in innate immunity that shed light on the pathophysiology of atopic dermatitis. Recent findings The mechanisms that promote the enhanced susceptibility to cutaneous infections in atopic dermatitis are complex interactions among several factors. They include skin barrier dysfunction, reduced skin lipid content, and abnormalities of the innate immune response. Some of the innate immune defects observed in atopic dermatitis are primary defects, such as epithelial barrier defects and defects in signaling or expression of innate receptors. Others may be secondary to the effects of the adaptive immune response. For example, deficiencies in antimicrobial peptides may be due to the overexpression of T helper 2 cytokines such as interleukin-4 and interleukin-13. However, how all components interact with each other remains to be fully investigated. Summary To break this vicious circle, a multiprolonged approach directed at healing or protecting the skin barrier and addressing the immune dysregulation is necessary to improve and control the disease.
引用
收藏
页码:463 / 468
页数:6
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