Factor VIII alloantibodies in hemophilia
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Hematology
Reference33 articles.
1. Haemophilia A: Mutation Type Determines Risk of Inhibitor Formation
2. Mechanism and Kinetics of Factor VIII Inactivation: Study With an IgG4 Monoclonal Antibody Derived From a Hemophilia A Patient With Inhibitor
3. A human antibody directed to the factor VIII C1 domain inhibits factor VIII cofactor activity and binding to von Willebrand factor
4. Phage Display Technology: A Tool to Explore the Diversity of Inhibitors to Blood Coagulation Factor VIII
5. Two classes of germline genes both derived from the VH1 family direct the formation of human antibodies that recognize distinct antigenic sites in the C2 domain of factor VIII
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1. Elimination of factor VIII-specific B cells by immunotoxins composed of a single factor VIII domain fused toPseudomonasexotoxin A;Journal of Thrombosis and Haemostasis;2018-10-08
2. Baboon envelope pseudotyped lentiviral vectors efficiently transduce human B cells and allow active factor IX B cell secretion in vivo in NOD / SCID γc ‐/‐ mice;Journal of Thrombosis and Haemostasis;2016-11-08
3. Induction of Immunological Tolerance to Transgene Products;The Immunological Barriers to Regenerative Medicine;2012-10-17
4. B-Cell-Delivered Gene Therapy Induces Functional T Regulatory Cells and Leads to a Loss of Antigen-Specific Effector Cells;Molecular Therapy;2010-08
5. Kinetics of factor VIII:C inhibitors and treatment response in severe hemophilia A patients;International Journal of Laboratory Hematology;2009-12
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