Immune tolerance therapy utilizing factor VIII/von Willebrand factor concentrate in haemophilia A patients with high titre factor VIII inhibitors

Haemophilia ◽  
2007 ◽  
Vol 0 (0) ◽  
pp. 071018054549002-???
Author(s):  
M. A. H. KURTH ◽  
D. DIMICHELE ◽  
C. SEXAUER ◽  
J. M. SANDERS ◽  
M. TORRES ◽  
...  
Blood ◽  
2004 ◽  
Vol 104 (11) ◽  
pp. 3096-3096
Author(s):  
Benoit Polack ◽  
Philippe Beurrier ◽  
Chantal Rothschild ◽  
Frédérique Orsini ◽  
Albert Faradji ◽  
...  

Abstract We report on 8 patients with severe haemophilia A and high responding anti-factor VIII (FVIII) inhibiting antibody in whom immune tolerance (IIT) was induced with a high purity plasma derived FVIII containing 14 to 20 IU/ml of von Willebrand factor (VWF) as a stabiliser. Their median ages at the diagnosis of the inhibitor was 10.6 months and ranged from 5 months to 9 years. At the onset of IIT, the median age was 1 year and 9 months and ranged from 9 months to 24.5 years. The median cumulative exposure days (CED) was 18.5 days and varied from 8 to 81 days when inhibitor was detected. The maximum level of inhibitor reached from 10 to 500 Bethesda Units (BU) with a median of 22.5 BU. Before inhibitor diagnosis 6 patients had received plasma derived high purity FVIII and 2 had received recombinant FVIII. The treatment schedule started with 50 IU/kg to 200 IU/kg FVIII every day. The time to reach an inhibitor level <1 BU was available for 5 patients; its median was 142 days and varied from 75 to 216 days. The treatment was considered successful when either the recovery or the half life of FVIII was normalized. The outcome was successful in 7 out of the 8 patients (87.5 %) who are now receiving FVIII concentrates either on demand or prophylactically. The last patient was considered as a partial success since the titre of his inhibitor was 0.8 BU and he could be treated by FVIII concentrates when needed. No definite IIT failure was observed in this cohort of patients. Since all the patients are by now back to FVIII treatment we can consider having a 100% success in IIT in this small cohort of patients. Therefore, despite the size of our cohort of patients, our study shows that high purity FVIII stabilized by VWF is an effective drug for the eradication of anti-FVIII inhibitors through induction of immune tolerance. Patients data Patient Age at FVIII 1st infussion Age at inhibitor diagnosis CED at inhibitor diagnosis Age at IIT Inhibitor max.titre (BU) Time (d) <1 BU IIT results N.A.; not available 1 9m 1y 9 1y 3m 52 93 Success 2 2d 4y 3m 81 4y 3m 21 N.A. Success 3 8y 10m 9y 33 24y 6m 30 N.A. Success 4 8m 10m 28 1y 8m 24 75 Success 5 8m 8.5m 8 9m 14.5 - Partial success 6 1y 1m 1y 10m 21 3y 1m 10 142 Success 7 6m 9m 10 11m 20 216 Success 8 4m 5m 16 1y 9m 500 176 Success


2010 ◽  
Vol 104 (11) ◽  
pp. 931-940 ◽  
Author(s):  
Giuseppe Lippi ◽  
Massimo Franchini

SummaryThe development of inhibitors that neutralise the function of factor VIII (FVIII) is currently not only the most challenging complication associated with the treatment of haemophilia A but it also increases the disease-related morbidity as bleeding episodes do not respond to standard therapy. The main short-term goal of the treatment of inhibitor patients is to control bleeding episodes while the long-term one is to permanently eradicate the inhibitor by immune tolerance induction, particularly in the case of high-titer antibodies. Due to some in vitro studies and clinical observations, some investigators have suggested that FVIII concentrates containing von Willebrand factor (VWF) may be less immunogenic than high-purity or recombinant FVIII products. It has also been suggested that success rates for immune tolerance induction are higher when plasma-derived FVIII products are used. The currently available data from laboratory and clinical studies on the role of VWF in inhibitor development and eradication in haemophilia A is critically analysed in this review. As a result, we have not found definitive evidence supporting a role for product type on inhibitor incidence and inhibitor eradication in haemophilia A patients.


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