医学
乌斯特基努马
阿达木单抗
依那西普
英夫利昔单抗
银屑病
耐受性
斑块性银屑病
皮肤病科
达巴万星
塞库金单抗
内科学
肿瘤科
银屑病性关节炎
不利影响
肿瘤坏死因子α
细菌
生物
万古霉素
金黄色葡萄球菌
遗传学
作者
Joyce Leman,A. David Burden
标识
DOI:10.1111/j.1365-2133.2012.11209.x
摘要
A number of biologic agents, including the tumour necrosis factor (TNF) antagonists etanercept, adalimumab and infliximab, and the interleukin (IL)-12/IL-23 antagonist ustekinumab, are available for the treatment of moderate-to-severe plaque psoriasis in the U.K. Currently, the selection of the first biologic, and the choice of sequential biologics in the event of efficacy/tolerability concerns, is made using a limited evidence base. The efficacy of biologics, the potential mechanisms of primary and secondary failure and the evidence for sequencing therapy among TNF antagonists and between TNF antagonists and IL-12/IL-23 blockade are reviewed. As psoriasis biologics registers begin to produce long-term safety and efficacy data, therapy decisions in plaque psoriasis may become more objective, and it may be possible to individualize treatment based on clinical or pharmacogenetic information.
科研通智能强力驱动
Strongly Powered by AbleSci AI