نتایج جستجو برای: fviii

تعداد نتایج: 1331  

2009
Maartje van den Biggelaar Alexander B. Meijer Jan Voorberg Koen Mertens

Weibel-Palade bodies (WPBs) are the endothelial storage organelles that are formed upon von Willebrand factor (VWF) expression. Apart from VWF, WPBs contain a variety of hemostatic and inflammatory proteins. Some of these are thought to be targeted to WPBs by directly interacting with VWF in the secretory pathway. Previous studies have demonstrated that coexpression of factor VIII (FVIII) with ...

Journal: :Thrombosis and haemostasis 2006
A Yaël Nossent Jeroen C J Eikenboom Hans L Vos Egbert Bakker Bea C Tanis Carine J M Doggen Rogier M Bertina Frits R Rosendaal

Levels of factor VIII (FVIII) are associated with the risk of venous thrombosis. The FVIII variation D1241E has been reported to be associated with decreased levels of FVIII. Our objective was to study whether D1241E is associated with levels of FVIII and the risk of venous thrombosis and whether this association is caused by D1241E or another linked variation. We analyzed the association of th...

Journal: :Blood 2005
John R Ohlfest Joel L Frandsen Sabine Fritz Paul D Lobitz Scott G Perkinson Karl J Clark Gary Nelsestuen Nigel S Key R Scott McIvor Perry B Hackett David A Largaespada

Hemophilia A is a lead candidate for treatment by gene therapy because small increments in the missing secreted protein product, coagulation factor VIII (FVIII), would result in substantial clinical amelioration. Clinically relevant therapy might be achieved by stably delivering a human FVIII cDNA to correct the bleeding disorder. We used the Sleeping Beauty (SB) transposon, delivered as naked ...

Journal: :Journal of thrombosis and haemostasis : JTH 2012
S R Selvaraj A N Scheller H Z Miao R J Kaufman Steven W Pipe

BACKGROUND Heterologous expression of factor VIII (FVIII) is about two to three orders of magnitude lower than similarly sized proteins. Bioengineering strategies aimed at different structural and biochemical attributes of FVIII have been successful in enhancing its expression levels. OBJECTIVE Disulfide bonds are vital to the proper folding, secretion and stability of most secretory proteins...

2004
Jean Guy G. Gilles Sabrina C. Grailly Marc De Maeyer Marc G. Jacquemin Luc P. VanderElst Jean-Marie R. Saint-Remy

Factor VIII (FVIII) administration elicits specific inhibitory antibodies (Abs) in about 25% of patients with hemophilia A. The majority of such Abs reacts with FVIII C2 domain. mAbBO2C11 is a high-affinity human monoclonal antibody (mAb) directed toward the C2 domain, which is representative of a major class of human FVIII inhibitors. Anti-idiotypic Abs were raised to mAbBO2C11 to establish th...

Journal: :Blood 2004
Christina Hausl Rafi U Ahmad Hans Peter Schwarz Eva M Muchitsch Peter L Turecek Friedrich Dorner Birgit M Reipert

Memory B cells are responsible for the rapidly emerging antibody response after antigen reexposure. The signals required for the restimulation of memory B cells have not been fully explained. We used a murine model of anti-factor VIII (FVIII) antibody responses in hemophilia A to study the requirements for the restimulation of FVIII-specific memory B cells and their differentiation into anti-FV...

Journal: :Blood 2000
R T Barrow J F Healey D Gailani D Scandella P Lollar

Factor VIII (fVIII) circulates as a heavy chain/light chain (A1-A2-B/ap-A3-C1-C2) heterodimer. The 41-residue light chain activation peptide, ap, is cleaved from fVIII during proteolytic activation by thrombin or factor Xa. We constructed 7 active recombinant hybrid B-domainless human/porcine fVIII molecules that contained combinations of porcine sequence replacements within the A2, ap-A3, and ...

Journal: :Haematologica 2007
Sandrine Delignat Suryasarathi Dasgupta Sébastien André Ana-Maria Navarrete Srinivas V Kaveri Jagadeesh Bayry Marie-Hélène André Sami Chtourou Zéra Tellier Sébastien Lacroix-Desmazes

Von Willebrand factor (VWF) has been proposed to reduce the immunogenicity of therapeutic factor VIII (FVIII) in patients with hemophilia A. Using FVIII-deficient mice, we compared the immunogenicity of different preparations of plasma-derived (pd) and recombinant (r) FVIII. Treatment of mice with pdFVIII induced significantly lower titers of FVIII inhibitors, as measured by ELISA and in vitro ...

Journal: :Journal of thrombosis and haemostasis : JTH 2015
B Boylan A S Rice A L Dunn M D Tarantino D B Brettler J C Barrett C H Miller

BACKGROUND The development of neutralizing antibodies, referred to as inhibitors, against factor VIII is a major complication associated with FVIII infusion therapy for the treatment of hemophilia A (HA). Previous studies have shown that a subset of HA patients and a low percentage of healthy individuals harbor non-neutralizing anti-FVIII antibodies that do not elicit the clinical manifestation...

2013
Zenjiro Sampei Tomoyuki Igawa Tetsuhiro Soeda Yukiko Okuyama-Nishida Chifumi Moriyama Tetsuya Wakabayashi Eriko Tanaka Atsushi Muto Tetsuo Kojima Takehisa Kitazawa Kazutaka Yoshihashi Aya Harada Miho Funaki Kenta Haraya Tatsuhiko Tachibana Sachiyo Suzuki Keiko Esaki Yoshiaki Nabuchi Kunihiro Hattori

In hemophilia A, routine prophylaxis with exogenous factor VIII (FVIII) requires frequent intravenous injections and can lead to the development of anti-FVIII alloantibodies (FVIII inhibitors). To overcome these drawbacks, we screened asymmetric bispecific IgG antibodies to factor IXa (FIXa) and factor X (FX), mimicking the FVIII cofactor function. Since the therapeutic potential of the lead bi...

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