Literature DB >> 26739399

Reduction of Factor VIII Inhibitor Titers During Immune Tolerance Induction With Recombinant Factor VIII-Fc Fusion Protein.

Charles L Groomes1,2, David M Gianferante2, Gary D Crouch1,2, Dina S Parekh1,2, David W Scott1, Kenneth Lieuw1,2.   

Abstract

The development of inhibitors toward factor VIII (FVIII) is a common and serious complication of hemophilia A (HA) therapy. Patients with hemophilia who develop inhibitors often undergo time- and resource-intensive immune tolerance induction (ITI) protocols. We report a 15-month-old male with severe HA and a high-titer inhibitor that occurred while receiving prophylactic treatment with recombinant FVIII (rFVIII), in whom significant inhibitor titer reduction was achieved with thrice weekly infusions of a new, prolonged half-life rFVIII-Fc fusion protein product (trade name Eloctate). Further studies are warranted to explore the potential of Eloctate in ITI protocols. Published 2016. This article is a U.S. Government work and is in the public domain in the USA.

Entities:  

Keywords:  eloctate; factor VIII inhibitors; hemophilia A; immune tolerance induction; recombinant factor VIII-Fc fusion protein

Mesh:

Substances:

Year:  2016        PMID: 26739399     DOI: 10.1002/pbc.25874

Source DB:  PubMed          Journal:  Pediatr Blood Cancer        ISSN: 1545-5009            Impact factor:   3.167


  15 in total

1.  Recombinant factor VIII Fc fusion protein drives regulatory macrophage polarization.

Authors:  Katalin Kis-Toth; Gaurav Manohar Rajani; Allison Simpson; Kate L Henry; Jennifer Dumont; Robert T Peters; Joe Salas; Christine Loh
Journal:  Blood Adv       Date:  2018-11-13

Review 2.  Practical aspects of extended half-life products for the treatment of haemophilia.

Authors:  Thierry Lambert; Gary Benson; Gerry Dolan; Cedric Hermans; Victor Jiménez-Yuste; Rolf Ljung; Massimo Morfini; Silva Zupančić-Šalek; Elena Santagostino
Journal:  Ther Adv Hematol       Date:  2018-09-06

Review 3.  What is the role of an extended half-life product in immune tolerance induction in a patient with severe hemophilia A and high-titer inhibitors?

Authors:  Maissaa Janbain; Steven Pipe
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2016-12-02

Review 4.  New therapies for hemophilia.

Authors:  Steven W Pipe
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2016-12-02

5.  Tolerogenic form of Factor VIII to prevent inhibitor development in the treatment of Hemophilia A.

Authors:  Nhan H Nguyen; Robert K Dingman; Sathy V Balu-Iyer
Journal:  J Thromb Haemost       Date:  2021-09-01       Impact factor: 16.036

Review 6.  Tolerogenic properties of the Fc portion of IgG and its relevance to the treatment and management of hemophilia

Authors:  Richard S Blumberg; David Lillicrap
Journal:  Blood       Date:  2018-03-27       Impact factor: 22.113

Review 7.  Novel approaches to hemophilia therapy: successes and challenges.

Authors:  Valder R Arruda; Bhavya S Doshi; Benjamin J Samelson-Jones
Journal:  Blood       Date:  2017-10-10       Impact factor: 22.113

Review 8.  Potential role of a new PEGylated recombinant factor VIII for hemophilia A.

Authors:  Tung Thanh Wynn; Burak Gumuscu
Journal:  J Blood Med       Date:  2016-06-20

Review 9.  Many factor VIII products available in the treatment of hemophilia A: an embarrassment of riches?

Authors:  Kenneth Lieuw
Journal:  J Blood Med       Date:  2017-06-15

Review 10.  Emerging therapies for hemophilia: controversies and unanswered questions.

Authors:  Valder R Arruda; Bhavya S Doshi; Benjamin J Samelson-Jones
Journal:  F1000Res       Date:  2018-04-24
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