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[高剂量FVIII与脉冲式静脉注射免疫球蛋白诱导免疫耐受]

[Immune tolerance induction with high-dose FVIII and pulsed intravenous immunoglobulin].

作者信息

Stiefel M, Pinkwart C, Haase R, Merkel N, Forsberg D, Mauz-Körholz C

机构信息

Universitätsklinik und Poliklinik für Kinder- und Jugendmedizin, Ernst-Grube Str. 40, 06120 Halle, Germany.

出版信息

Hamostaseologie. 2010 Nov;30 Suppl 1:S119-21.

Abstract

UNLABELLED

The development of neutralizing allo-antibodies against factor VIII (FVIII) or FVIII inhibitors is a severe complication in the treatment of haemophilia A. About 25% of the children with severe haemophilia A develop FVIII inhibitors. Here we report on a boy with severe haemophilia A and intron 22 inversion of the FVIII gene who was diagnosed at ten months of age. After 16 exposure days to FVIII (81 days after initial exposure) he developed a FVIII inhibitor (maximum: 9.76 BU/ml).

THERAPY

We started immune tolerance induction (ITI) according to the Bonn protocol with high dose plasma derived FVIII concentrate (100 IU per kg body weight) twice daily. For additional inhibitor elimination treatment the patient received intravenous immunoglobulin (ivIg) at a dose of 1-2 g/kg body weight every 4 to 6 weeks. After start of treatment a rapid decline of the inhibitor level was observed, nevertheless low FVIII inhibitor levels persisted (<5 BU/ml). Furthermore, the FVIII half-life was still accelerated. However, after every course of ivIg the inhibitor level declined and FVIII half-life was prolonged. Currently, the FVIII half-life is approaching normal values after more than seven months of ITI duration.

CONCLUSION

Additional application of immunoglobulin is beneficial for immune tolerance induction.

摘要

未标记

针对凝血因子VIII(FVIII)产生中和性同种抗体或FVIII抑制剂是A型血友病治疗中的严重并发症。约25%的重度A型血友病儿童会产生FVIII抑制剂。在此,我们报告一名10个月大时被诊断为重度A型血友病且FVIII基因内含子22倒位的男孩。在接触FVIII 16天(初次接触后81天)后,他产生了FVIII抑制剂(最高值:9.76 BU/ml)。

治疗

我们按照波恩方案开始免疫耐受诱导(ITI),每天两次给予高剂量血浆源性FVIII浓缩物(每千克体重100 IU)。为进行额外的抑制剂清除治疗,患者每4至6周接受一次剂量为1 - 2 g/kg体重的静脉注射免疫球蛋白(ivIg)。开始治疗后,观察到抑制剂水平迅速下降,但低水平的FVIII抑制剂仍持续存在(<5 BU/ml)。此外,FVIII半衰期仍加快。然而,每次给予ivIg疗程后,抑制剂水平下降,FVIII半衰期延长。目前,经过超过7个月的ITI疗程,FVIII半衰期接近正常水平。

结论

额外应用免疫球蛋白对免疫耐受诱导有益。

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