Department of Dermatology, Emory University School of Medicine, Atlanta, Georgia.
Department of Dermatology, Emory University School of Medicine, Atlanta, Georgia.
J Am Acad Dermatol. 2018 Mar;78(3 Suppl 1):S63-S66. doi: 10.1016/j.jaad.2017.12.023. Epub 2017 Dec 15.
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.
瞬时受体电位 (TRP) 离子通道是全身感觉信号转导的重要介质。在过去的十年中,我们对 TRP 对多种皮肤生理过程的贡献的理解有了很大的提高。TRP 阳离子通道亚家族 V 成员 1 (TRPV1) 是该大型离子通道家族中研究较为深入的成员之一,它影响瘙痒涉及的多种途径。此外,TRPV1 似乎在维持皮肤屏障功能中发挥作用。这些特性使 TRPV1 成为特应性皮炎新疗法的成熟靶点。神经激肽拮抗剂可能影响类似的途径,并已对此进行了研究。早期试验数据表明,这些疗法是安全的,但由于我们正在等待 II 期和 III 期临床试验数据的公布,因此评估它们在特应性皮炎中的疗效仍有待观察。