Effect of short-term liver X receptor activation on epidermal barrier features in mild to moderate atopic dermatitis

丝状蛋白 斯科拉德 特应性皮炎 经皮失水 洛里克林 湿疹面积及严重程度指数 总苞素 胸腺基质淋巴细胞生成素 医学 耐受性 促炎细胞因子 势垒函数 免疫学 内科学 银屑病 生物 炎症 病理 角质形成细胞 不利影响 角质层 皮肤科生活质量指数 生物化学 体外 细胞生物学
作者
Tali Czarnowicki,Anders B. Dohlman,Kunal Malik,Diane Antonini,Robert Bissonnette,Tom C. Chan,Lisa Zhou,Huei‐Chi Wen,Yeriel Estrada,Hui Xu,Catherine Bryson,Jie Shen,Deepak S. Lala,Avi Ma’ayan,Gerard M. McGeehan,Richard E. Gregg,Emma Guttman‐Yassky
出处
期刊:Annals of Allergy Asthma & Immunology [Elsevier BV]
卷期号:120 (6): 631-640.e11 被引量:32
标识
DOI:10.1016/j.anai.2018.03.013
摘要

Background Liver X receptors (LXRs) are involved in maintaining epidermal barrier and suppressing inflammatory responses in model systems. The LXR agonist VTP-38543 showed promising results in improving barrier function and inflammatory responses in model systems. Objective To assess the safety, tolerability, cellular and molecular changes, and clinical efficacy of the topical VTP-38543 in adults with mild to moderate atopic dermatitis (AD). Methods A total of 104 ambulatory patients with mild to moderate AD were enrolled in this randomized, double-blind, vehicle-controlled trial between December 2015 and September 2016. VTP-38543 cream in 3 concentrations (0.05%, 0.15%, and 1.0%) or placebo was applied twice daily for 28 days. Pretreatment and posttreatment skin biopsy specimens were obtained from a subset of 33 patients. Changes in SCORing of Atopic Dermatitis, Eczema Area and Severity Index, Investigator's Global Assessment, and tissue biomarkers (by real-time polymerase chain reaction and immunostaining) were evaluated. Results Topical VTP-38543 was safe and well tolerated. VTP-38543 significantly increased messenger RNA (mRNA) expression of epidermal barrier differentiation (loricrin and filaggrin, P = .02) and lipid (adenosine triphosphate–binding cassette subfamily G member 1 and sterol regulatory element binding protein 1c, P < .01) measures and reduced epidermal hyperplasia markers (thickness, keratin 16 mRNA). VTP-38543 nonsignificantly suppressed cellular infiltrates and down-regulated mRNA expression of several TH17/TH22-related (phosphatidylinositol 3, S100 calcium-binding protein A12) and innate immunity (interleukin 6) markers. Conclusion Topical VTP-38543 is safe and well tolerated. Its application led to improvement in barrier differentiation and lipids. Longer-term studies are needed to clarify whether a barrier-based approach can induce meaningful suppression of immune abnormalities. Trial Registration clinicaltrials.gov Identifier: NCT02655679.

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