Literature DB >> 15849524

Role of von Willebrand factor in immune tolerance induction.

Carmen Escuriola Ettingshausen1, Wolfhart Kreuz.   

Abstract

Patients with hemophilia who develop inhibitors present a particular challenge in therapeutic management. Although such patients are at high risk for severe bleeding episodes, the optimal treatment approach--prophylaxis--is ineffective unless inhibitors are eliminated. Several protocols for immune tolerance induction have been used. Success rates may vary depending both on patient variables and on factors related to the therapeutic regimen, including concentrate purity and von Willebrand factor (VWF) content. Several in vitro studies testing inhibitor plasma samples against various factor VIII (FVIII) concentrates have shown lower FVIII inhibitor titer compared with concentrates with greater VWF content. Recent in vivo observations also support the importance of VWF content, based on evidence of reduced rates of success of immune tolerance induction with use of the high-purity FVIII products that became available in the early 1990s. Current data thus support use of FVIII concentrates containing VWF in immune tolerance induction; other variables may also contribute to the relative success of this treatment. Studies are needed to delineate these variables in order to improve management of this potentially devastating complication of hemophilia treatment.

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Year:  2005        PMID: 15849524     DOI: 10.1097/01.mbc.0000167660.30886.e9

Source DB:  PubMed          Journal:  Blood Coagul Fibrinolysis        ISSN: 0957-5235            Impact factor:   1.276


  4 in total

1.  Successful immune tolerance induction with factor VIII/von Willebrand factor concentrate in an elderly patient with severe haemophilia A and a high responder inhibitor.

Authors:  Gianna Franca Rivolta; Caterina Di Perna; Massimo Franchini; Federica Riccardi; Luigi Ippolito; Maria Lombardi; Annarita Tagliaferri
Journal:  Blood Transfus       Date:  2010-01       Impact factor: 3.443

Review 2.  Management of haemophilia A-inhibitor patients: clinical and regulatory perspectives.

Authors:  Zera Tellier; Marie-Hélène André; Benoît Polack
Journal:  Clin Rev Allergy Immunol       Date:  2009-10       Impact factor: 8.667

Review 3.  Optimal use of recombinant factor VIIa in the control of bleeding episodes in hemophilic patients.

Authors:  John Puetz
Journal:  Drug Des Devel Ther       Date:  2010-07-21       Impact factor: 4.162

Review 4.  Human von Willebrand factor/factor VIII concentrates in the management of pediatric patients with von Willebrand disease/hemophilia A.

Authors:  Giancarlo Castaman; Silvia Linari
Journal:  Ther Clin Risk Manag       Date:  2016-06-30       Impact factor: 2.423

  4 in total

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