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抑制剂的流行病学及当前治疗策略。

Epidemiology of inhibitors and current treatment strategies.

作者信息

Kreuz Wolfhart, Ettingshausen Carmen Escuriola, Auerswald Günter, Saguer Inmaculada Martinez, Becker Sabine, Funk Markus, Heller Christine, Klarmann Dieter, Klingebiel Thomas

机构信息

Centre of Pediatrics III, Department of Hematology and Oncology, Comprehensive Care Center of Thrombosis and Hemostasis Johann-Wolfgang-Goethe-University Hospital, Frankfurt am Main, Germany.

出版信息

Haematologica. 2003 Jun;88(6):EREP04.

Abstract

The development of inhibitors is currently one of the most serious complications in the treatment of hemophilic children. Prospective studies of previously untreated patients (PUP) showed that up to 52% of patients with severe hemophilia A developed inhibitors during the first 50 exposure days (ED) (>100 for outliers). Inhibitor development is influenced by the type of hemophilia, the severity and the type of mutation. No significant differences in inhibitor incidence were found in prospective studies conducted with plasma-derived or recombinant products. However, no comparative study has been finished yet. A still ongoing prospective, multi-center PUP-study initiated by the German, Austrian and the Swiss Society of Thrombosis and Hemostasis Research (GTH) foresees the direct comparison of different types of concentrates with regard to inhibitor development. Preliminary results (update February 2002) show a slightly higher inhibitor development (p=0.08) in severely affected hemophilia A patients treated with recombinant factor (F) VIII concentrates. However, the groups are very small and statistically reliable statements cannot be made at the moment. In case of inhibitor development rapid inhibitor elimination and immune tolerance induction (ITI) is the preferred way to reduce the high risk of bleeding episodes. In this respect, various therapeutic regimens, such as the administration of high doses of FVIII twice daily (Bonn protocol), or lower doses three times weekly (van Creveld protocol), have been attempted. Elimination of inhibitors from plasma by immune adsorption followed by immune suppression (Malmö protocol) has also been used. The influence of the type of concentrate used for ITI has never been investigated comparatively. A longitudinal study of ITI at our center showed a significantly decreased success rate since the introduction of high purity plasma derived and recombinant FVIII products using the Bonn protocol. In inhibitor patients who showed an unsatisfactory response to treatment with FVIII concentrates with very little or no VWF the change to concentrates containing high amounts of von Willebrand factor (VWF) increased success rates up to 90%. These observations raise the question of whether VWF plays an important role in the induction of immune tolerance.

摘要

目前,抑制剂的产生是血友病患儿治疗过程中最严重的并发症之一。对既往未接受治疗患者(PUP)的前瞻性研究表明,高达52%的重度甲型血友病患者在最初50个暴露日(ED)(异常值>100)期间产生了抑制剂。抑制剂的产生受血友病类型、严重程度及突变类型的影响。在使用血浆源性或重组产品进行的前瞻性研究中,未发现抑制剂发生率有显著差异。然而,尚无比较研究完成。由德国、奥地利和瑞士血栓与止血研究学会(GTH)发起的一项仍在进行的前瞻性多中心PUP研究预计将对不同类型的凝血因子浓缩剂在抑制剂产生方面进行直接比较。初步结果(2002年2月更新)显示,接受重组凝血因子(F)VIII浓缩剂治疗的重度甲型血友病患者中,抑制剂产生率略高(p=0.08)。然而,各研究组规模很小,目前无法做出统计学上可靠的陈述。如果产生了抑制剂,快速清除抑制剂和诱导免疫耐受(ITI)是降低出血发作高风险的首选方法。在这方面,已经尝试了各种治疗方案,例如每日两次给予高剂量FVIII(波恩方案),或每周三次给予较低剂量(范克里维尔德方案)。通过免疫吸附从血浆中清除抑制剂,随后进行免疫抑制(马尔默方案)也已被采用。从未对用于ITI的浓缩剂类型的影响进行过比较研究。我们中心对ITI的一项纵向研究表明,自采用波恩方案引入高纯度血浆源性和重组FVIII产品以来,成功率显著下降。在对FVIII浓缩剂治疗反应不佳的抑制剂患者中,若FVIII浓缩剂含很少或不含血管性血友病因子(VWF),改用含大量VWF的浓缩剂后成功率提高至90%。这些观察结果引发了一个问题,即VWF在免疫耐受诱导中是否起重要作用。

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