Inhibitors in hemophilia A: mechanisms of inhibition, management and perspectives

NM Ananyeva, S Lacroix-Desmazes… - Blood coagulation & …, 2004 - journals.lww.com
Factor VIII (FVIII) replacement therapy remains the mainstay in hemophilia A care. The major
complication of replacement therapy is formation of antibodies, which inhibit FVIII activity …

Do proteolytic antibodies complete the panoply of the autoimmune response in acquired haemophilia A?

A Mahendra, S Padiolleau‐Lefevre… - British journal of …, 2012 - Wiley Online Library
Acquired haemophilia A (AHA) is a rare bleeding disorder characterized by the sudden
generation of autoantibodies against factor VIII (FVIII) in individuals with no previous history …

Profiling humoral autoimmune repertoire of dilated cardiomyopathy (DCM) patients and development of a disease‐associated protein chip

S Horn, A Lueking, D Murphy, A Staudt, C Gutjahr… - …, 2006 - Wiley Online Library
Dilated cardiomyopathy (DCM) is a myocardial disease characterized by progressive
depression of myocardial contractile function and ventricular dilatation. Thirty percent of …

Nonneutralizing FVIII-specific antibody signatures in patients with hemophilia A and in healthy donors

H Schweiger, J Rejtő, CJ Hofbauer, V Berg… - Blood …, 2022 - ashpublications.org
Previous studies identified nonneutralizing FVIII-specific antibodies in the circulation of
severe and nonsevere hemophilia A (sHA and nsHA) patients without FVIII inhibitors and …

B-cell and T-cell epitopes in anti-factor VIII immune responses

KP Pratt, AR Thompson - Clinical reviews in allergy & immunology, 2009 - Springer
Adequate hemostasis is achieved for many hemophilia A patients by infusion of plasma-
derived or recombinant factor VIII (FVIII), but unfortunately, a significant subset of patients …

A chromogenic substrate method for detecting and titrating anti-factor VIII antibodies in the presence of lupus anticoagulant

AN Blanco, AA Peirano, SH Grosso, LC Gennari… - …, 2002 - haematologica.org
BACKGROUND AND OBJECTIVES. The development of neutralizing anti-factor VIII
antibodies (a-fVIII) is a major clinical complication. Lupus anticoagulant (LA) might affect …

[HTML][HTML] Factor VIII-hydrolyzing IgG in acquired and congenital hemophilia

B Wootla, A Mahendra, JD Dimitrov, A Friboulet… - FEBS letters, 2009 - Elsevier
Anti-factor VIII (FVIII) inhibitory IgG may arise as allo-antibodies to therapeutic FVIII in
patients with congenital hemophilia A, or as auto-antibodies to endogenous FVIII in …

Comparative analysis of antigen specificities in the monomeric and dimeric fractions of intravenous immunoglobulin

SM Miescher, A Schaub, M Ghielmetti… - Annals of the New …, 2005 - Wiley Online Library
Intravenous immunoglobulin (IVIG) preparations are derived from the pooled plasma of
thousands of healthy donors and contain a complex mix of antibodies. Depending on the …

Иммунный механизм регуляции системы гемостаза: роль каталитических аутоантител-абзимов

Б Кузник, НН Цыбиков - Тромбоз, гемостаз и реология, 2011 - elibrary.ru
В обзоре приведены собственные данные и сведения литературы о роли аутоантител
к факторам свертывания крови, естественным антикоагулянтам и фибринолитическим …

Targets of autoantibodies in acquired hemophilia A are not restricted to factor VIII: data from the GTH-AH 01/2010 study

O Oleshko, S Werwitzke, A Klingberg, T Witte… - Blood …, 2023 - ashpublications.org
The root cause of autoantibody formation against factor VIII (FVIII) in acquired hemophilia A
(AHA) remains unclear. We aimed to assess whether AHA is exclusively associated with …