Suppr超能文献

在高反应不良风险的血友病A抑制物患者中,使用高纯度血管性血友病因子/ VIII复合物浓缩物诱导免疫耐受。

Immune tolerance induction with a high purity von Willebrand factor/VIII complex concentrate in haemophilia A patients with inhibitors at high risk of a poor response.

作者信息

Gringeri A, Musso R, Mazzucconi M G, Piseddu G, Schiavoni M, Pignoloni P, Mannucci P M

机构信息

A. Bianchi Bonomi Haemophilia and Thrombosis Centre, Department of Medicine and Medical Specialties, University of Milan and IRCCS Maggiore Hospital, Milan, Italy.

出版信息

Haemophilia. 2007 Jul;13(4):373-9. doi: 10.1111/j.1365-2516.2007.01484.x.

Abstract

Immune tolerance induction (ITI) is effective in approximately 70% of haemophilia patients with inhibitors. Poor prognostic factors are age >6 years, ITI started >1 year from inhibitor development, inhibitor peaks >200 BU, inhibitor titre >10 BU when ITI is started and previously failed ITI. The objective of this study was to identify the effectiveness in ITI of a high purity von Willebrand factor/factor VIII (VWF/FVIII) complex concentrate in inhibitor patients at high risk of failure. Patients with severe or moderate haemophilia A and high responding inhibitors who had at least one poor prognostic factor for ITI failure were prospectively followed-up. Success was defined by undetectable inhibitor, recovery and half life >66% of expected values. ITI dose regimens were chosen by each haemophilia centre. Seventeen haemophiliacs (16 severe, one moderate), aged 4-54 years (median 23) were followed-up for 6-71 months. Poor prognostic factors were delayed-onset ITI (n = 16), age >6 years (n = 16), previously failed ITI (n = 4), inhibitor peak >200 BU (n = 2) and inhibitor >10 BU when ITI was started (n = 4). Complete success was obtained in nine patients (53%) after 4-30 months of treatment (median 24), including two of four patients who had previously failed ITI. Seven patients achieved a partial success, with sustained low inhibitor titres (median 1.5 BU, range 1.1-2.8) but abnormal recovery and/or half-life, while the remaining patient withdrew ITI after 12 months when the inhibitor titer was still 70 BU. These findings suggest that high purity VWF/FVIII complex concentrates are effective in ITI, even in patients at high risk of failure.

摘要

免疫耐受诱导(ITI)对约70%的血友病抑制物患者有效。预后不良因素包括年龄>6岁、ITI在抑制物产生后>1年开始、抑制物峰值>200 BU、开始ITI时抑制物滴度>10 BU以及既往ITI失败。本研究的目的是确定高纯度血管性血友病因子/凝血因子VIII(VWF/FVIII)复合浓缩物对有高失败风险的抑制物患者进行ITI治疗的有效性。对患有重度或中度甲型血友病且抑制物反应高且至少有一个ITI失败预后不良因素的患者进行前瞻性随访。成功的定义为抑制物检测不到、恢复且半衰期>预期值的66%。每个血友病中心选择ITI剂量方案。17例血友病患者(16例重度,1例中度),年龄4 - 54岁(中位数23岁),随访6 - 71个月。预后不良因素包括延迟启动ITI(n = 16)、年龄>6岁(n = 16)、既往ITI失败(n = 4)、抑制物峰值>200 BU(n = 2)以及开始ITI时抑制物>10 BU(n = 4)。9例患者(53%)在治疗4 - 30个月(中位数24个月)后获得完全成功,包括4例既往ITI失败患者中的2例。7例患者获得部分成功,抑制物滴度持续较低(中位数1.5 BU,范围1.1 - 2.8),但恢复和/或半衰期异常,而其余1例患者在12个月后当抑制物滴度仍为70 BU时停止ITI治疗。这些发现表明,高纯度VWF/FVIII复合浓缩物在ITI治疗中有效,即使对有高失败风险的患者也是如此。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验