von Willebrand factor and transforming growth factor-beta modulate immune response against coagulation factor VIII in FVIII-deficient mice
Author:
Publisher
Elsevier BV
Subject
Hematology
Reference36 articles.
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2. Influence of the type of factor VIII concentrate on the incidence of factor VIII inhibitors in previously untreated patients with severe hemophilia A;Goudemand;Blood,2006
3. Mechanisms of TGF-beta signaling in regulation of cell growth and differentiation;Moustakas;Immunol Lett,2002
4. Transforming growth factor-beta in T-cell biology;Gorelik;Nat Rev Immunol,2002
5. Effect of factor VIII concentrate on leucocyte cytokine production: characterization of TGF-beta as an immunomodulatory component in plasma-derived factor VIII concentrate;Hodge;Br J Haematol,1999
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1. Binding Promiscuity of Therapeutic Factor VIII;Thrombosis and Haemostasis;2024-07-01
2. The C1 and C2 domains of blood coagulation factor VIII mediate its endocytosis by dendritic cells;Haematologica;2016-10-06
3. Key insights to understand the immunogenicity of FVIII products;Thrombosis and Haemostasis;2016
4. Alloantibodies to therapeutic factor VIII in hemophilia A: the role of von Willebrand factor in regulating factor VIII immunogenicity;Haematologica;2015-01-31
5. Dangerous liaisons: how the immune system deals with factor VIII;Journal of Thrombosis and Haemostasis;2013-01
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