Immune tolerance induction in haemophilia A patients with high-responding inhibitors to factor VIII: experience at a single institution

Citation
A. Rocino et al., Immune tolerance induction in haemophilia A patients with high-responding inhibitors to factor VIII: experience at a single institution, HAEMOPHILIA, 7(1), 2001, pp. 33-38
Citations number
27
Categorie Soggetti
Hematology
Journal title
HAEMOPHILIA
ISSN journal
13518216 → ACNP
Volume
7
Issue
1
Year of publication
2001
Pages
33 - 38
Database
ISI
SICI code
1351-8216(200101)7:1<33:ITIIHA>2.0.ZU;2-#
Abstract
Inhibitor antibodies to transfused factor VIII pose significant challenges in the management of haemophilia A patients. The main concern is the ineffi cacy of replacement therapy in patients with high-titre antibodies, who hav e a shorter life-span and a greater morbidity compared to subjects without inhibitors. The ultimate goal in treating these patients is to eliminate th e inhibitor antibody entirely, allowing the recommencement of specific repl acement therapy. The results of an immune tolerance regimen based on pharma cokinetic parameters are reported here. In 12 high-responder haemophilia A patients immune tolerance induction (ITI) was attempted with daily administ ration of factor VIII concentrates of very high purity, either plasma-deriv ed or produced by recombinant-DNA technology. Patients were given 100 IU kg (-1) day(-1) until the inhibitor was shown to be absent by at least two neg ative assays 1 month apart, with normal recovery of infused factor VIII and normal half-life (> 6 h), as assessed after a 3-day washout period. After the patient was judged to be inhibitor-free, immune tolerance treatment was continued with unmodified factor VIII doses for 2 months. Doses were there after gradually reduced and finally, regular prophylaxis by administration of 25 TU kg(-1) three times weekly was instituted. Immune tolerance was ach ieved in 10 of the 12 patients (including six of seven with long-standing i nhibitors) within a median time of 8 months. Outcome of immune tolerance wa s not influenced by age at start of ITI nor by the interval between inhibit or development and ITI. The success rate and the inhibitor disappearance ti me of our immune tolerance regimen, utilizing high-purity factor VIII, agre es with those reported by other investigators.