Zaghi Daniel, Krueger Gerald G, Callis Duffin Kristina
Department of Dermatology, School of Medicine, University of Utah School of Medicine, Salt Lake City, UT 84132, USA.
J Drugs Dermatol. 2012 Feb;11(2):160-7.
Psoriasis is a complex, multigenic immune/inflammatory-mediated disorder that variably affects the skin, nails, and joints. In September 2009, ustekinumab (Stelara®), a monoclonal antibody that targets interleukin 12 (IL-12) and 23 (IL-23), was approved in the United States for treatment of moderate-to-severe plaque psoriasis. The drug's mechanism of action is derived from extensive immunologic and genomic research identifying IL-12 and IL-23 of the Th1 and Th17 inflammatory pathways, respectively, as key mediators of psoriasis. Ustekinumab is a completely human monoclonal antibody to the shared p40 subunit of IL-12 and IL-23. The drug has demonstrated efficacy, short-term safety, and convenience of use in the treatment of plaque psoriasis and psoriatic arthritis. Though long-term safety concerns remain, ustekinumab adds to the current treatment armamentarium and holds promise to improve quality of life. This is a concise and current review of ustekinumab in the treatment of plaque psoriasis and psoriatic arthritis, with focus on data from the seven published clinical trials.
银屑病是一种复杂的、多基因免疫/炎症介导的疾病,可不同程度地影响皮肤、指甲和关节。2009年9月,优特克单抗(喜达诺®),一种靶向白细胞介素12(IL-12)和23(IL-23)的单克隆抗体,在美国被批准用于治疗中度至重度斑块状银屑病。该药物的作用机制源自广泛的免疫学和基因组学研究,分别确定Th1和Th17炎症途径中的IL-12和IL-23为银屑病的关键介质。优特克单抗是一种针对IL-12和IL-23共享p40亚基的完全人源化单克隆抗体。该药物在治疗斑块状银屑病和银屑病关节炎方面已显示出疗效、短期安全性和使用便利性。尽管长期安全性问题仍然存在,但优特克单抗增加了当前的治疗手段,并有望改善生活质量。这是一篇关于优特克单抗治疗斑块状银屑病和银屑病关节炎的简明且最新的综述,重点关注七项已发表临床试验的数据。