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Native-like aggregates of Factor VIII (FVIII) are immunogenic von Willebrand Factor deficient and hemophilia A mice

The administration of recombinant Factor VIII (FVIII) is the first line therapy for Hemophilia A (HA), but 25–35% of patients develop an inhibitory antibody response. In general, the presence of aggregates contributes to unwanted immunogenic responses against therapeutic proteins. FVIII has been sho...

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Detalhes bibliográficos
Main Authors: Pisal, Dipak S., Kosloski, Matthew P., Middaugh, C. Russell, Bankert, Richard B., Balu-Iyer, Sathy V.
Formato: Artigo
Idioma:Inglês
Publicado em: 2012
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3774159/
https://ncbi.nlm.nih.gov/pubmed/22388918
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jps.23091
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