Aries Peer M, Lamprecht Peter, Gross Wolfgang L
University Hospital Schleswig-Holstein, Campus Luebeck, Department of Rheumatology and Rheumaklinik Bad Bramstedt, Ratzeburger Allee 160, 23538 Lübeck, Germany.
Expert Opin Biol Ther. 2007 Apr;7(4):521-33. doi: 10.1517/14712598.7.4.521.
Biological therapies enable us to apply highly selective targeting components to modulate the immune response. Until now, a few controlled studies investigated the efficacy of TNF-alpha blocking agents in systemic vasculitis have been carried out, but, in general, they were falling short of expectations. However, there is conducive evidence that TNF-alpha blockers are advantageous in antineutrophil cytoplasmic antibodies (ANCA)-associated vasculitis, at least in selected disease stages. Likewise, although the efficacy of the monoclonal CD20 antibody rituximab in ANCA-associated vasculitis is obvious, the effect on predominantly granulomatous disease activity in Wegener's granulomatosis is less clear. In addition, interferon-alpha is used for induction treatment particularly in Churg-Strauss syndrome. Even though the effectiveness and safety of short-term administration was confirmed by case series, severe side effects after long-term treatment relativized the initial results. This review presents the recent data on the use of biologicals in vasculitis and appraises the knowledge in the clinical context.
生物疗法使我们能够应用高度选择性的靶向成分来调节免疫反应。到目前为止,已经开展了一些关于肿瘤坏死因子-α(TNF-α)阻断剂在系统性血管炎中疗效的对照研究,但总体而言,这些研究并未达到预期效果。然而,有有利证据表明,TNF-α阻断剂在抗中性粒细胞胞浆抗体(ANCA)相关血管炎中具有优势,至少在特定疾病阶段如此。同样,尽管单克隆CD20抗体利妥昔单抗在ANCA相关血管炎中的疗效明显,但对韦格纳肉芽肿主要肉芽肿性疾病活动的影响尚不清楚。此外,α干扰素尤其用于变应性肉芽肿性血管炎的诱导治疗。尽管病例系列证实了短期给药的有效性和安全性,但长期治疗后的严重副作用使最初的结果有所折扣。本综述介绍了血管炎中生物制剂使用的最新数据,并在临床背景下评估了相关知识。