Division of Dermatology, Baylor University Medical Center, Dallas, TX, USA.
Expert Rev Clin Immunol. 2014 Feb;10(2):189-202. doi: 10.1586/1744666X.2014.878649.
Ustekinumab is a fully human monoclonal antibody directed against the p40 subunit shared by interleukin 12 and interleukin 23, two naturally occurring protein regulators that play an important role in immune-mediated inflammatory diseases, including psoriatic arthritis (PsA). In September of 2009, the US FDA approved ustekinumab for the treatment of adult patients with moderate to severe plaque psoriasis. Beginning in November of 2009, Janssen Biotech (formerly Centocor Biotech), the developer of ustekinumab, initiated clinical trials to investigate the efficacy of ustekinumab in the treatment of other inflammatory disorders, including PsA. Phase II and Phase III studies showed both a good safety profile and significant efficacy for ustekinumab in the treatment of PsA, leading to the drug's approval in both Europe and the USA. In an immunotherapy market currently dominated by anti-TNF-α drugs for the treatment of PsA, ustekinumab offers an alternative option for patients with PsA, including those unresponsive to methotrexate and the TNF-α inhibitory agents currently approved for this potentially debilitating disease.
乌司奴单抗是一种针对白细胞介素 12 和白细胞介素 23 的 p40 亚单位的全人源单克隆抗体,这两种天然存在的蛋白质调节剂在免疫介导的炎症性疾病中发挥着重要作用,包括银屑病关节炎(PsA)。2009 年 9 月,美国食品药品监督管理局(FDA)批准乌司奴单抗用于治疗中重度斑块状银屑病的成年患者。2009 年 11 月开始,乌司奴单抗的开发商詹森生物科技(原先名为千禧制药)启动了临床试验,以研究乌司奴单抗在治疗其他炎症性疾病,包括银屑病关节炎中的疗效。Ⅱ期和Ⅲ期研究表明,乌司奴单抗在治疗银屑病关节炎方面具有良好的安全性和显著疗效,这使得该药物在欧洲和美国获得批准。在目前以抗 TNF-α 药物为主导的银屑病关节炎免疫疗法市场中,乌司奴单抗为包括对甲氨蝶呤和目前批准用于治疗这种潜在致残性疾病的 TNF-α 抑制剂无应答的银屑病关节炎患者提供了一种替代选择。