The immune response to factor VIII and the development of inhibitory antibodies is a complex multi-factorial process involving a variety of immune regulatory genes and cells, several of which have the potential to determine risk. A better understanding of the mechanisms involved will increase the likelihood of development of new therapeutic options for patients with hemophilia. This review summarizes genetic and non-genetic risk factors currently under evaluation, and the potential modulative effect of the von Willebrand factor on factor VIII immuno- and antigenicity. In addition, the role of T-regulatory cells in the pathogenicity of inhibitors will be discussed. © 2008 The Authors Journal compilation © 2008 Blackwell Publishing Ltd.
CITATION STYLE
Astermark, J., Lacroix-Desmazes, S., & Reding, M. T. (2008, July). Inhibitor development. Haemophilia. https://doi.org/10.1111/j.1365-2516.2008.01711.x
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