Chiricozzi Andrea, Faleri Sara, Saraceno Rosita, Bianchi Luca, Buonomo Oreste, Chimenti Sergio, Chimenti Maria Sole
Dermatology Department, University of Rome Tor Vergata, Rome, Italy.
Expert Rev Clin Immunol. 2015 Apr;11(4):443-55. doi: 10.1586/1744666X.2015.1013534. Epub 2015 Feb 10.
Because of the increased knowledge about the underlying cytokine network in psoriasis, selective systemic agents for the treatment of moderate-to-severe psoriasis have been developed during the past decade. The marked upregulation of JAK/STAT pathways in psoriasis and the identification of multiple key mediators in psoriasis pathogenesis that signal through JAK/STAT pathways led to investigation of JAK proteins as potential therapeutic targets for psoriasis treatment. A novel JAK-STAT inhibitor, tofacitinib, has been tested in preclinical studies for the treatment of psoriasis. Considering the satisfactory safety profile and the encouraging efficacy observed in the Phase II and Phase III trials, tofacitinib may represent an important therapeutic to be included into the psoriasis paradigm.
由于对银屑病潜在细胞因子网络的认识不断增加,在过去十年中已开发出用于治疗中重度银屑病的选择性全身用药。银屑病中JAK/STAT通路的显著上调以及银屑病发病机制中通过JAK/STAT通路发出信号的多种关键介质的鉴定,促使人们研究JAK蛋白作为银屑病治疗的潜在靶点。一种新型JAK-STAT抑制剂托法替布已在治疗银屑病的临床前研究中进行了测试。鉴于在II期和III期试验中观察到的令人满意的安全性和令人鼓舞的疗效,托法替布可能成为银屑病治疗模式中的一种重要治疗药物。