Antibodies to factor VIII in hemophilia A patients

Citation
Hh. Brackmann et al., Antibodies to factor VIII in hemophilia A patients, VOX SANGUIN, 78, 2000, pp. 187-190
Citations number
35
Categorie Soggetti
Cardiovascular & Hematology Research
Journal title
VOX SANGUINIS
ISSN journal
00429007 → ACNP
Volume
78
Year of publication
2000
Supplement
2
Pages
187 - 190
Database
ISI
SICI code
0042-9007(2000)78:<187:ATFVIH>2.0.ZU;2-B
Abstract
Inhibitor development represents the main complication in the treatment of haemophilia A. The risk of inhibitor formation is in part genetically deter mined by the type of the underlying factor VIII gene lesion but environment al factors may also play an important role. Due to the lack of efficiency o f factor VIII in these patients other therapeutic agents must be used for t he treatment of bleedings, however, none is as effective as factor VIII in a non-inhibitor patient. Therefore, the eridication of the inhibitor throug h immune tolerance therapy is the treatment of choice. Centralized national and international immune tolerance registries have collected the results a nd show cost effectiveness of this treatment.