Emerging therapies for atopic dermatitis: TRPV1 antagonists

被引:30
|
作者
Bonchak, Jonathan G. [1 ]
Swerlick, Robert A. [1 ]
机构
[1] Emory Univ, Sch Med, Dept Dermatol, 1525 Clifton Rd,Suite 100, Atlanta, GA 30329 USA
关键词
atopic dermatitis; clinical trials; pruritus; skin barrier; transient receptor potential; TRPV1/substance P inhibitors; ITCH; SAFETY;
D O I
10.1016/j.jaad.2017.12.023
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Transient receptor potential (TRP) ion channels are important mediators of somatosensory signaling throughout the body. Our understanding of the contribution of TRPs to a multitude of cutaneous physiologic processes has grown substantially in the past decade. TRP cation channel subfamily V member 1 (TRPV1), one of the better-understood members of this large family of ion channels, affects multiple pathways involved in pruritus. Further, TRPV1 appears to play a role in maintaining skin barrier function. Together, these properties make TRPV1 a ripe target for new therapies in atopic dermatitis. Neurokinin antagonists may affect similar pathways and have been studied to this effect. Early trials data suggest that these therapies are safe, but assessment of their efficacy in atopic dermatitis is pending as we await publication of phase II and III clinical trials data. (J Am Acad Dermatol 2018; 78: S63-6.)
引用
收藏
页码:S63 / S66
页数:4
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