Literature DB >> 25638804

Alloantibodies to therapeutic factor VIII in hemophilia A: the role of von Willebrand factor in regulating factor VIII immunogenicity.

Johannes Oldenburg1, Sébastien Lacroix-Desmazes2, David Lillicrap3.   

Abstract

The rising incidence of neutralizing antibodies (inhibitors) against therapeutic factor VIII prompted the conduct of studies to answer the question as to whether this rise is related to the introduction of recombinant factor VIII products. The present article summarizes current opinions and results of non-clinical and clinical studies on the immunogenic potential of recombinant compared to plasma-derived factor VIII concentrates. Numerous studies provided circumstantial evidence that von Willebrand factor, the natural chaperone protein present in plasma-derived factor VIII products, plays an important role in protecting exogenous factor VIII from uptake by antigen presenting cells and from recognition by immune effectors. However, the definite contribution of von Willebrand factor in reducing the inhibitor risk and in the achievement of immune tolerance is still under debate. Copyright© Ferrata Storti Foundation.

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Year:  2015        PMID: 25638804      PMCID: PMC4803147          DOI: 10.3324/haematol.2014.112821

Source DB:  PubMed          Journal:  Haematologica        ISSN: 0390-6078            Impact factor:   9.941


  96 in total

1.  The use of factor VIII/von Willebrand factor concentrate for immune tolerance induction in haemophilia A patients with high-titre inhibitors: association of clinical outcome with inhibitor epitope profile.

Authors:  D A Greninger; J M Saint-Remy; M Jacquemin; A Benhida; D M DiMichele
Journal:  Haemophilia       Date:  2007-12-12       Impact factor: 4.287

2.  Concentrate-related inhibitor risk: is a difference always real?

Authors:  A Iorio; M Marcucci; M Makris
Journal:  J Thromb Haemost       Date:  2011-11       Impact factor: 5.824

Review 3.  More than a decade of international experience with a pdFVIII/VWF concentrate in immune tolerance.

Authors:  E Santagostino
Journal:  Haemophilia       Date:  2013-01       Impact factor: 4.287

4.  Identification and functional importance of tyrosine sulfate residues within recombinant factor VIII.

Authors:  D D Pittman; J H Wang; R J Kaufman
Journal:  Biochemistry       Date:  1992-04-07       Impact factor: 3.162

5.  VWF protects FVIII from endocytosis by dendritic cells and subsequent presentation to immune effectors.

Authors:  Suryasarathi Dasgupta; Yohann Repessé; Jagadeesh Bayry; Ana-Maria Navarrete; Bharath Wootla; Sandrine Delignat; Theano Irinopoulou; Caroline Kamaté; Jean-Marie Saint-Remy; Marc Jacquemin; Peter J Lenting; Annie Borel-Derlon; Srinivas V Kaveri; Sébastien Lacroix-Desmazes
Journal:  Blood       Date:  2006-09-19       Impact factor: 22.113

6.  Induction of tolerance to factor VIII by transient co-administration with rapamycin.

Authors:  B Moghimi; B K Sack; S Nayak; D M Markusic; C S Mah; R W Herzog
Journal:  J Thromb Haemost       Date:  2011-08       Impact factor: 5.824

7.  Clotting factor concentrate switching and inhibitor development in hemophilia A.

Authors:  Alfonso Iorio; Paolo Puccetti; Mike Makris
Journal:  Blood       Date:  2012-06-12       Impact factor: 22.113

8.  Factor VIII inhibitor antibodies with C2 domain specificity are less inhibitory to factor VIII complexed with von Willebrand factor.

Authors:  T Suzuki; M Arai; K Amano; K Kagawa; K Fukutake
Journal:  Thromb Haemost       Date:  1996-11       Impact factor: 5.249

9.  International workshop on immune tolerance induction: consensus recommendations.

Authors:  D M DiMichele; W K Hoots; S W Pipe; G E Rivard; E Santagostino
Journal:  Haemophilia       Date:  2007-07       Impact factor: 4.287

10.  Kinetics of factor VIII-von Willebrand factor association.

Authors:  A J Vlot; S J Koppelman; J C Meijers; C Dama; H M van den Berg; B N Bouma; J J Sixma; G M Willems
Journal:  Blood       Date:  1996-03-01       Impact factor: 22.113

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  11 in total

1.  von Willebrand factor binds to the surface of dendritic cells and modulates peptide presentation of factor VIII.

Authors:  Nicoletta Sorvillo; Robin B Hartholt; Esther Bloem; Magdalena Sedek; Anja ten Brinke; Carmen van der Zwaan; Floris P van Alphen; Alexander B Meijer; Jan Voorberg
Journal:  Haematologica       Date:  2015-12-03       Impact factor: 9.941

2.  Micromanaging Tolerance in Hemophilia A Gene Therapy.

Authors:  Jennielle Jobson; Brian D Brown
Journal:  Mol Ther       Date:  2017-06-16       Impact factor: 11.454

3.  The C1 and C2 domains of blood coagulation factor VIII mediate its endocytosis by dendritic cells.

Authors:  Bagirath Gangadharan; Mathieu Ing; Sandrine Delignat; Ivan Peyron; Maud Teyssandier; Srinivas V Kaveri; Sébastien Lacroix-Desmazes
Journal:  Haematologica       Date:  2016-10-06       Impact factor: 9.941

4.  Immune Tolerance Induction (ITI) with a pdFVIII/VWF Concentrate (octanate) in 100 Patients in the Observational ITI (ObsITI) Study.

Authors:  Carmen Escuriola Ettingshausen; Vladimír Vdovin; Nadezhda Zozulya; Pavel Svirin; Tatiana Andreeva; Majda Benedik-Dolničar; Victor Jiménez-Yuste; Lidija Kitanovski; Silva Zupancic-Šalek; Anna Pavlova; Angelika Bátorová; Cesar Montaño Mejía; Gulnara Abdilova; Sigurd Knaub; Martina Jansen; Shannely Lowndes; Larisa Belyanskaya; Olaf Walter; Johannes Oldenburg
Journal:  TH Open       Date:  2022-05-26

5.  Peptides identified on monocyte-derived dendritic cells: a marker for clinical immunogenicity to FVIII products.

Authors:  Wojciech Jankowski; Yara Park; Joseph McGill; Eugene Maraskovsky; Marco Hofmann; Vincent P Diego; Bernadette W Luu; Tom E Howard; Roberta Kellerman; Nigel S Key; Zuben E Sauna
Journal:  Blood Adv       Date:  2019-05-14

6.  Low-dose immune tolerance induction therapy in children of Arab descent with severe haemophilia A, high inhibitor titres and poor prognostic factors for immune tolerance induction treatment success.

Authors:  Mohsen Elalfy; Islam Elghamry; Hoda Hassab; Omar Elalfy; Nevine Andrawes; Magdy El-Ekiaby
Journal:  Haemophilia       Date:  2021-11-19       Impact factor: 4.263

7.  Long-term course of anti-factor VIII antibody in patients with hemophilia A at a single center.

Authors:  Ki Young Yoo; Sang Chun Joo; Yong Mook Choi
Journal:  Blood Res       Date:  2016-03-25

8.  Navigating Speed Bumps on the Innovation Highway in Hemophilia Therapeutics.

Authors:  Donna M DiMichele
Journal:  Hemasphere       Date:  2018-10-02

9.  Analyses of the FranceCoag cohort support differences in immunogenicity among one plasma-derived and two recombinant factor VIII brands in boys with severe hemophilia A.

Authors:  Thierry Calvez; Hervé Chambost; Roseline d'Oiron; Vincent Dalibard; Virginie Demiguel; Alexandra Doncarli; Yves Gruel; Yoann Huguenin; Patrice Lutz; Chantal Rothschild; Christine Vinciguerra; Jenny Goudemand
Journal:  Haematologica       Date:  2017-10-12       Impact factor: 9.941

10.  Simoctocog Alfa (Nuwiq) in Previously Untreated Patients with Severe Haemophilia A: Final Results of the NuProtect Study.

Authors:  Ri J Liesner; Aby Abraham; Carmen Altisent; Mark J Belletrutti; Manuel Carcao; Manuela Carvalho; Hervé Chambost; Anthony K C Chan; Leonid Dubey; Jonathan Ducore; Michael Gattens; Paolo Gresele; Yves Gruel; Benoit Guillet; Victor Jimenez-Yuste; Lidija Kitanovski; Anna Klukowska; Sunil Lohade; Maria Elisa Mancuso; Johannes Oldenburg; Anna Pavlova; Berardino Pollio; Marianne Sigaud; Vladimir Vdovin; Kateryna Vilchevska; John K M Wu; Martina Jansen; Larisa Belyanskaya; Olaf Walter; Sigurd Knaub; Ellis J Neufeld
Journal:  Thromb Haemost       Date:  2021-02-13       Impact factor: 5.249

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