Emerging Treatment Options in Atopic Dermatitis: Topical Therapies

被引:83
作者
Nygaard, Uffe [1 ]
Deleuran, Mette [1 ]
Vestergaard, Christian [1 ]
机构
[1] Aarhus Univ Hosp, Dept Dermatol & Venereol, PP Orumsgade 11, DK-8000 Aarhus C, Denmark
关键词
Atopic dermatitis; Eczema; Pruritus; Topical treatment; Calcineurin inhibitors; Corticosteroids; Phosphodiesterase-4; inhibitors; JAK inhibitors; PHOSPHODIESTERASE-4 INHIBITOR E6005; ATTENTION-DEFICIT/HYPERACTIVITY DISORDER; LINOLENIC ACID PREVENTS; DOUBLE-BLIND; PDE4; INHIBITOR; SKIN BARRIER; CALCINEURIN INHIBITORS; TRPV1; ANTAGONIST; OPEN-LABEL; PHASE; 2A;
D O I
10.1159/000484407
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Atopic dermatitis is a chronic inflammatory skin disorder affecting children and adults, with the majority presenting mild to moderate disease severity. The use of topical corticosteroids (TCSs) in combination with emollients has been the mainstay for treating mild to moderate atopic dermatitis since the 1950s, and as a supplement to systemic treatment in severe disease. However, while very effective, TCSs are often accompanied by poor adherence due to corticophobia (fear of using corticosteroids in patients or doctors), unwanted side effects, and in some cases insufficient clinical response. Topical calcineurin inhibitors (TCIs) are able to inhibit the activation of T-lymphocytes and thereby diminish inflammation. In some patients the use of TCIs has been limited due to a localized burning sensation on the first days of treatment, and also due to fear of other adverse effects. Consequently, there has been a need for the development of new topical products for atopic dermatitis. Novel topical therapies are in the pipeline and comprise both new doses and formulations of well-known pharmaceutical molecules and novel approaches targeting unique inflammatory pathways and mechanisms of disease, with a promise of higher efficacy and less harmful side effects. We review topical drugs in the pipeline for atopic dermatitis, and focus on those available in the clinicaltrials.gov database with a first received date from January 1, 2014 to May 31, 2017. (c) 2017 S. Karger AG, Basel
引用
收藏
页码:333 / 343
页数:11
相关论文
共 102 条
[1]   Dihomo-γ-linolenic acid prevents the development of atopic dermatitis through prostaglandin D1 production in NC/Tnd mice [J].
Amagai, Yosuke ;
Oida, Kumiko ;
Matsuda, Akira ;
Jung, Kyungsook ;
Kakutani, Said ;
Tanaka, Takao ;
Matsuda, Kenshiro ;
Jang, Hyosun ;
Ahn, Ginae ;
Xia, Yan ;
Kawashima, Hiroshi ;
Shibata, Hiroshi ;
Matsuda, Hiroshi ;
Tanaka, Akane .
JOURNAL OF DERMATOLOGICAL SCIENCE, 2015, 79 (01) :30-37
[2]   Comorbidities of Atopic Dermatitis: Beyond Rhinitis and Asthma [J].
Andersen Y.M.F. ;
Egeberg A. ;
Skov L. ;
Thyssen J.P. .
Current Dermatology Reports, 2017, 6 (1) :35-41
[3]   Involvement of Leukotriene B4 Released from Keratinocytes in Itch-associated Response to Intradermal Interleukin-31 in Mice [J].
Andoh, Tsugunobu ;
Harada, Ayako ;
Kuraishi, Yasushi .
ACTA DERMATO-VENEREOLOGICA, 2017, 97 (08) :922-927
[4]  
[Anonymous], ORL DERM AESTH CLIN
[5]   Biomarkers in atopic dermatitis: it is time to stratify [J].
Ardern-Jones, M. R. ;
Bieber, T. .
BRITISH JOURNAL OF DERMATOLOGY, 2014, 171 (02) :207-208
[6]   Management of Difficult-to-Treat Atopic Dermatitis [J].
Arkwright, Peter D. ;
Motala, Cassim ;
Subramanian, Hamsa ;
Spergel, Jonathan ;
Schneider, Lynda C. ;
Wollenberg, Andreas .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY-IN PRACTICE, 2013, 1 (02) :142-151
[7]  
Baeumer Wolfgang, 2007, Inflammation & Allergy Drug Targets, V6, P17, DOI 10.2174/187152807780077318
[8]  
Bao Lei, 2013, JAKSTAT, V2, pe24137, DOI 10.4161/jkst.24137
[9]   Atopic dermatitis 2.0: from the clinical phenotype to the molecular taxonomy and stratified medicine [J].
Bieber, Th. .
ALLERGY, 2012, 67 (12) :1475-1482
[10]   Mechanisms of disease: Atopic dermatitis [J].
Bieber, Thomas .
NEW ENGLAND JOURNAL OF MEDICINE, 2008, 358 (14) :1483-1494