Tobacco Inc, Toxicology Research Laboratories, Central Pharmaceutical Research Institute, Kanagawa, Japan.
Toxicol Pathol. 2020 Dec;48(8):1008-1016. doi: 10.1177/0192623320970896. Epub 2020 Dec 2.
Delgocitinib ointment 0.5% is the world's first topical Janus kinase inhibitor product and was approved for treatment of atopic dermatitis (AD) in Japan. Although topical corticosteroids (TCSs) have been the mainstay of pharmacotherapy in AD over the past decades, long-term use of TCSs causes skin atrophy and alteration of the epidermal tight junction (TJ) leading to epidermal barrier dysfunction. In this study, delgocitinib ointment 0.5% or representative TCSs of different potencies were applied dermally once daily to the ear pinna of normal ICR mice for 14 days, and ear pinna thickness, histopathology, and immunohistochemistry for epidermal TJ proteins claudin-1 and -4 were evaluated. All the TCSs caused decreases in ear pinna thickness with epidermal thinning, sebaceous gland atrophy, and atrophy/decreased number of the subcutaneous adipocytes and decreased immunohistochemical staining intensity for epidermal claudins. In contrast, delgocitinib ointment 0.5% did not cause any of those changes. In conclusion, once daily topical delgocitinib ointment 0.5% for 14 days did not cause skin atrophy or decreased immunohistochemical staining of epidermal claudins, which are common safety concerns associated with TCSs. These characteristics suggest that delgocitinib ointment 0.5% has an improved safety profile over currently available TCS therapies particular for the long-term AD treatment.
0.5%地夸磷索钠软膏是全球首款局部应用的 Janus 激酶抑制剂产品,已在日本获批用于治疗特应性皮炎(AD)。尽管皮质类固醇(TCSs)在过去几十年中一直是 AD 药物治疗的主要方法,但长期使用 TCSs 会导致皮肤萎缩和表皮紧密连接(TJ)改变,从而导致表皮屏障功能障碍。在这项研究中,将 0.5%地夸磷索钠软膏或不同效力的代表性 TCSs 每天一次涂于正常 ICR 小鼠的耳郭,持续 14 天,评估耳郭厚度、组织病理学和表皮 TJ 蛋白闭合蛋白-1 和 -4 的免疫组织化学。所有 TCSs 均导致耳郭厚度减小,表皮变薄、皮脂腺萎缩、皮下脂肪细胞萎缩/减少,表皮闭合蛋白的免疫组织化学染色强度降低。相比之下,0.5%地夸磷索钠软膏未引起任何这些变化。总之,每天一次局部应用 0.5%地夸磷索钠软膏 14 天不会导致皮肤萎缩或表皮闭合蛋白免疫组织化学染色降低,这是与 TCSs 相关的常见安全性问题。这些特征表明,0.5%地夸磷索钠软膏与目前可用的 TCS 治疗方法相比,具有更好的安全性,特别是在长期 AD 治疗方面。