Analysis of Factor VIII Inhibitors Using Hybrid Human/Porcine Factor VIII
- 1 June 1997
- journal article
- review article
- Published by Georg Thieme Verlag KG in Thrombosis and Haemostasis
- Vol. 78 (01) , 647-651
- https://doi.org/10.1055/s-0038-1657605
Abstract
Recombinant hybrid human/porcine factor VIII molecules have been used to map a major determinant of the epitope recognized by human anti-factor VIII A2 domain inhibitory antibodies to a region bounded by human fVIII residues Arg484-Ile508. This approach is being used to characterize the C2 domain inhibitor epitope. The process of creating hybrid human/porcine factor VIII molecules to map inhibitor epitopes produces procoagulantly active fVIII with reduced reactivity with clinically significant factor VIII inhibitors. This suggests that it may be possible to develop of a hybrid human/porcine factor VIII that is useful in the management of hemophilia A and acquired hemophilia.Keywords
This publication has 13 references indexed in Scilit:
- Residues 484-508 Contain a Major Determinant of the Inhibitory Epitope in the A2 Domain of Human Factor VIIIJournal of Biological Chemistry, 1995
- Sequence of the Murine Factor VIII cDNAGenomics, 1993
- [17]Gene splicing by overlap extensionPublished by Elsevier ,1993
- High resolution functional analysis of antibody-antigen interactionsJournal of Molecular Biology, 1992
- Epitopes on protein antigens: Misconceptions and realitiesCell, 1990
- Molecular basis of factor VIII inhibition by human antibodies. Antibodies that bind to the factor VIII light chain prevent the interaction of factor VIII with phospholipid.Journal of Clinical Investigation, 1989
- Receptor and Antibody Epitopes in Human Growth Hormone Identified by Homolog-Scanning MutagenesisScience, 1989
- Epitope mapping of human factor VIII inhibitor antibodies by deletion analysis of factor VIII fragments expressed in Escherichia coli.Proceedings of the National Academy of Sciences, 1988
- Localization of human factor FVIII inhibitor epitopes to two polypeptide fragments.Proceedings of the National Academy of Sciences, 1985
- Structure of human factor VIIINature, 1984