Literature DB >> 24360854

Future treatment options for atopic dermatitis - small molecules and beyond.

Knut Schäkel1, Thomas Döbel2, Ina Bosselmann2.   

Abstract

Atopic dermatitis (AD) is a common eczematous skin disease with a chronic and relapsing course. Current therapeutic options for moderate to severe AD in children and adults are unsatisfactory. Along with the success of basic research to define pathogenesis-related targets, novel small molecule inhibitors and biologics for the treatment of AD have been developed. These compounds focus on the specific reduction of pruritus, interfere with the pro-allergic Th2-deviation of the immune system or inhibit inflammatory pathways in the skin. Based on studies registered at ClinicalTrials.gov we present novel treatment strategies of AD, their molecular mechanisms of action, and discuss the current status of the clinical results. As many of the new compounds target pathogenesis-related traits of the disease, we face a new era in the treatment and understanding of AD.
Copyright © 2013 Japanese Society for Investigative Dermatology. Published by Elsevier Ireland Ltd. All rights reserved.

Entities:  

Keywords:  Atopic dermatitis; IgE; Pruritus; Review; Th2; Therapy

Mesh:

Substances:

Year:  2013        PMID: 24360854     DOI: 10.1016/j.jdermsci.2013.11.009

Source DB:  PubMed          Journal:  J Dermatol Sci        ISSN: 0923-1811            Impact factor:   4.563


  4 in total

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Authors:  Sewoong Kim; Dongrae Cho; Jihun Kim; Manjae Kim; Sangyeon Youn; Jae Eun Jang; Minkyu Je; Dong Hun Lee; Boreom Lee; Daniel L Farkas; Jae Youn Hwang
Journal:  Biomed Opt Express       Date:  2016-11-28       Impact factor: 3.732

2.  SERPINB3/B4 contributes to early inflammation and barrier dysfunction in an experimental murine model of atopic dermatitis.

Authors:  Umasundari Sivaprasad; Kayla G Kinker; Mark B Ericksen; Mark Lindsey; Aaron M Gibson; Stacey A Bass; Nicolas S Hershey; Jingyuan Deng; Mario Medvedovic; Gurjit K Khurana Hershey
Journal:  J Invest Dermatol       Date:  2014-08-11       Impact factor: 8.551

3.  IL-1β-Induced Protection of Keratinocytes against Staphylococcus aureus-Secreted Proteases Is Mediated by Human β-Defensin 2.

Authors:  Bingjie Wang; Brian J McHugh; Ayub Qureshi; Dominic J Campopiano; David J Clarke; J Ross Fitzgerald; Julia R Dorin; Richard Weller; Donald J Davidson
Journal:  J Invest Dermatol       Date:  2016-10-01       Impact factor: 8.551

4.  Determining the Value of Two Biologic Drugs for Chronic Inflammatory Skin Diseases: Results of a Multi-Criteria Decision Analysis.

Authors:  Néboa Zozaya; Lucía Martínez-Galdeano; Bleric Alcalá; Jose Carlos Armario-Hita; Concepción Carmona; Jose Manuel Carrascosa; Pedro Herranz; María Jesús Lamas; Marta Trapero-Bertran; Álvaro Hidalgo-Vega
Journal:  BioDrugs       Date:  2018-06       Impact factor: 5.807

  4 in total

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