Weisenseel Peter, Prinz Jörg Christoph
Department of Dermatology, Ludwig-Maximilians-University, Munich, Germany.
Cutis. 2006 Sep;78(3):197-9.
Generalized pustular psoriasis is a dramatic potentially life-threatening psoriasis variant and represents a major therapeutic challenge. Tumor necrosis factor alpha (TNF-alpha) inhibitors have been shown to be highly effective in psoriasis vulgaris and psoriasis arthritis. Currently, TNF-alpha can be targeted therapeutically by 2 different approaches. TNF-alpha antibodies show a fast onset of action and a long-lasting activity. Soluble TNF-alpha receptors have a slower onset and a shorter duration of activity, which allows a rapid cessation of the drug's activity in the case of adverse events. Here we report that a remission of generalized pustular psoriasis achieved by the TNF-alpha antibody infliximab was maintained by long-term application of the soluble TNF-alpha receptor etanercept. Sequential therapy with TNF-alpha antibodies and TNF-alpha receptors may represent a novel concept that combines a rapid onset of action in the initiation therapy with a lower risk for severe adverse events in the maintenance treatment of pustular psoriasis.
泛发性脓疱型银屑病是一种严重的、可能危及生命的银屑病变体,是一个重大的治疗挑战。肿瘤坏死因子α(TNF-α)抑制剂已被证明在寻常型银屑病和银屑病关节炎中非常有效。目前,TNF-α可以通过两种不同的方法进行靶向治疗。TNF-α抗体起效快且活性持久。可溶性TNF-α受体起效较慢且活性持续时间较短,这使得在出现不良事件时能够迅速停止药物活性。在此我们报告,通过长期应用可溶性TNF-α受体依那西普可维持由TNF-α抗体英夫利昔单抗实现的泛发性脓疱型银屑病缓解。TNF-α抗体和TNF-α受体序贯治疗可能代表了一种新的概念,即将初始治疗中的快速起效与脓疱型银屑病维持治疗中严重不良事件风险较低相结合。