Human factor IX corrects the bleeding diathesis of mice with hemophilia B.
Publication/Presentation Date
2-1-1998
Abstract
Mice with hemophilia B have been engineered using gene targeting techniques. These animals exhibit severe factor IX deficiency and a clinical phenotype that mirrors the human disease. We have bred the founder animals onto two different strains of mice, C57B1/6 and CD-1, and have sought to determine whether adenoviral vectors expressing human factor IX could correct the bleeding diathesis of mice with hemophilia B. Initial experiments showed that purified plasma-derived human factor IX added to murine factor IX-deficient plasma resulted in complete correction of the activated partial thromboplastin time (aPTT), and that injection of 10(11) particles of an adenoviral vector expressing human factor IX resulted in normalization of a modified aPTT in mouse plasma. As an additional method of assessing the function of human factor IX in the murine coagulation system, bleeding times were performed in normal, hemophilic, and adenoviral-treated hemophilic mice. By two different bleeding-time techniques, the treated hemophilic mice gave values identical to normal littermate controls, whereas the untreated hemophilic mice exhibited heavy blood loss and prolonged bleeding. There was a marked difference in antibody formation in the two strains of mice; 100% of the hemophilic CD-1 mice formed antibodies to human factor IX, but none of the C57B1/6 mice did. These data suggest that the C57B1/6 hemophilic mice will be more useful for gene transfer studies, while the CD-1 hemophilic mice may be of greater utility in studying the development of inhibitors.
Volume
91
Issue
3
First Page
784
Last Page
790
ISSN
0006-4971
Published In/Presented At
Kung, S. H., Hagstrom, J. N., Cass, D., Tai, S. J., Lin, H. F., Stafford, D. W., & High, K. A. (1998). Human factor IX corrects the bleeding diathesis of mice with hemophilia B. Blood, 91(3), 784–790.
Disciplines
Medicine and Health Sciences | Pediatrics
PubMedID
9446637
Department(s)
Department of Pediatrics
Document Type
Article