创新之痒:芳基烃受体激动剂作为特应性皮炎未来疗法的作用。

IF 3.7 4区 医学 Q1 DERMATOLOGY Clinical and Experimental Dermatology Pub Date : 2024-11-21 DOI:10.1093/ced/llae502
Areen Wazir, Edel A O'Toole
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引用次数: 0

摘要

特应性皮炎(AD)是一种慢性炎症性皮肤病,影响着全球 2 亿多人,患者通常表现为皮肤干燥、瘙痒和疼痛。寻找特应性皮炎最佳治疗方法所面临的挑战源于该疾病的异质性及其多方面的病因:皮肤屏障功能障碍、免疫系统失调、遗传因素、环境因素和皮肤微生物的改变。皮质类固醇激素、钙调磷酸酶抑制剂和免疫抑制剂等传统的 AD 治疗方法存在一些局限性,如停药后症状复发、缺乏靶向作用和不良反应风险。本文献综述旨在探讨和总结芳基烃受体(AHR)激动剂(即塔皮那洛夫)作为未来治疗 AD 的潜在药物的作用。AHR 激动剂有望克服传统 AD 疗法的局限性,通过维持皮肤屏障的完整性、抵御氧化应激、调节免疫活动和炎症以及恢复健康的皮肤微生物群来发挥其治疗价值。Tapinarof是一种局部AHR激动剂,目前正在进行3期试验(ADORING 3),显示出良好的效果。要将 Tapinarof 纳入注意力缺失症的治疗途径,必须在大量不同的患者群体中,对其在不同注意力缺失症亚型中的疗效、持久性、潜在缓解作用和安全性进行进一步研究。此外,还需要考虑 Tapinarof 与外用药相比的成本效益,并需要研究人员、临床医生和政策制定者之间的多学科合作。
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Itching for innovation: role of aryl hydrocarbon receptor agonists as a future therapy for atopic dermatitis.

Atopic dermatitis (AD) is a chronic, inflammatory skin condition which affects over 200 million people worldwide, with patients commonly presenting with dry, itchy and sore skin. The challenge in finding optimal treatment for AD stems from the heterogenous nature of the disease and its multifaceted aetiology: skin barrier dysfunction, immune system dysregulation, genetic factors, environmental factors and alterations in skin microorganisms. Traditional treatments for AD such as corticosteroids, calcineurin inhibitors and immunosuppressants have several limitations such as reoccurrence of symptoms when discontinued, lack of targeted action and risk of adverse effects. The aim of this literature review was to explore and summarise the role of aryl hydrocarbon receptor (AHR) agonists (namely Tapinarof) as potential future therapy for AD. AHR agonists hope to overcome the limitations of traditional AD therapies and exert their therapeutic value by maintaining integrity of the skin barrier, defending against oxidative stress, modulating immune activity and inflammation and restoring a healthy skin microbiome. Tapinarof, a topical AHR agonist, is showing promising results and is currently in phase 3 trials (ADORING 3). For Tapinarof to be integrated into the AD treatment pathway, further research must be conducted on its efficacy, durability, potential remittive effect and safety across different AD subtypes in a large, diverse patient population. In addition, Tapinarof's cost-effectiveness compared to its topical counterparts needs to be considered and multidisciplinary collaboration is required between researchers, clinicians and policy makers.

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来源期刊
CiteScore
3.20
自引率
2.40%
发文量
389
审稿时长
3-8 weeks
期刊介绍: Clinical and Experimental Dermatology (CED) is a unique provider of relevant and educational material for practising clinicians and dermatological researchers. We support continuing professional development (CPD) of dermatology specialists to advance the understanding, management and treatment of skin disease in order to improve patient outcomes.
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