Atopic dermatitis - Perspectives and unmet medical needs

被引:0
|
作者
Buhl, Timo [1 ,2 ]
Werfel, Thomas [3 ,4 ]
机构
[1] Univ Med Ctr Gottingen, Dept Dermatol Venereol & Allergol, Robert Koch Str 40, Gottingen D-37075, Germany
[2] Univ Gottingen, Lower Saxony Inst Occupat Dermatol, Gottingen, Germany
[3] Hannover Med Sch, Dept Dermatol & Allergy, Div Immunodermatol & Allergy Res, Hannover, Germany
[4] Hannover Med Sch, Lower Saxony Inst Occupat Dermatol, Hannover, Germany
关键词
atopic eczema; contact allergic eczema; irritative-toxic eczema; JAK inhibitors; STAPHYLOCOCCUS-AUREUS; EFFICACY; PHASE-3; TRPV1; ITCH;
D O I
10.1111/ddg.15050
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Atopic dermatitis (AD) is a chronic inflammatory skin disease for which many new insights have been gained in recent years through a better understanding of pathophysiology, concomitant diseases and therapeutics in particular. In this review, new and practice-relevant results from current research are presented. Many studies have been performed on the diagnosis of AD and on different subtypes, yet no diagnostic biomarker or clinical predictor of treatment response has been established. For topical treatment, some agents such as Janus kinase (JAK) inhibitors are in advanced stages of clinical trials or already approved in some countries, which will be available in Europe for the treatment of certain eczema subtypes in the foreseeable future. Current systemic therapies in Europe include two antibodies for inhibition of the interleukin (IL)-4/13 signaling cascades and three oral JAK inhibitors with somewhat different efficacy and safety profiles. Among the antibody therapies for AD already advanced in development, promising new targets include blockade of IL-31, of neurokinin-1 receptor on sensory neurons, and inhibition of the OX40/OX40L axis for cutaneous dendritic cell and T lymphocyte interaction. Primary prevention and modulation of sequential disease progression as well as effects on concomitant diseases by early therapeutic intervention will be important questions in future research on AD.
引用
收藏
页码:354 / 354
页数:1
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