Literature DB >> 27136426

Towards personalised therapy for von Willebrand disease: a future role for recombinant products.

Emmanuel J Favaloro1.   

Abstract

von Willebrand disease (VWD) is reportedly the most common bleeding disorder and is caused by deficiencies and/or defects in the adhesive plasma protein von Willebrand factor (VWF). Functionally, normal VWF prevents bleeding by promoting both primary and secondary haemostasis. In respect to primary haemostasis, VWF binds to both platelets and sub-endothelial matrix components, especially collagen, to anchor platelets to damaged vascular tissue and promote thrombus formation. VWF also stabilises and protects factor VIII in the circulation, delivering FVIII to the site of injury, which then facilitates secondary haemostasis and fibrin formation/thrombus stabilisation. As a result of this, patients with VWD suffer a bleeding diathesis reflective of a primary defect caused by defective/deficient VWF, which in some patients is compounded by a reduction in FVIII. Management of VWD, therefore, chiefly entails replacement of VWF, and sometimes also FVIII, to protect against bleeding. The current report principally focuses on the future potential for "personalised" management of VWD, given the emerging options in recombinant therapies. Recombinant VWF has been developed and is undergoing clinical trials, and this promising therapy may soon change the way in which VWD is managed. In particular, we can envisage a personalised treatment approach using recombinant VWF, with or without recombinant FVIII, depending on the type of VWD, the extent of deficiencies, and the period and duration of treatment.

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Year:  2016        PMID: 27136426      PMCID: PMC4918558          DOI: 10.2450/2016.0258-15

Source DB:  PubMed          Journal:  Blood Transfus        ISSN: 1723-2007            Impact factor:   3.443


  80 in total

1.  Phase II prospective open-label trial of recombinant interleukin-11 in women with mild von Willebrand disease and refractory menorrhagia.

Authors:  Margaret V Ragni; Rachel C Jankowitz; Kristen Jaworski; Elizabeth P Merricks; Mark T Kloos; Timothy C Nichols
Journal:  Thromb Haemost       Date:  2011-08-11       Impact factor: 5.249

Review 2.  Diagnosis and classification of von Willebrand disease: a review of the differential utility of various functional von Willebrand factor assays.

Authors:  Emmanuel J Favaloro
Journal:  Blood Coagul Fibrinolysis       Date:  2011-10       Impact factor: 1.276

Review 3.  Newer Hemostatic Agents.

Authors:  Massimo Franchini; Emmanuel J Favaloro; Giuseppe Lippi
Journal:  Semin Thromb Hemost       Date:  2015-04-20       Impact factor: 4.180

Review 4.  Biological therapies for von Willebrand disease.

Authors:  Emmanuel J Favaloro; Massimo Franchini; Giuseppe Lippi
Journal:  Expert Opin Biol Ther       Date:  2012-03-20       Impact factor: 4.388

5.  Characterisation of a novel high-purity, double virus inactivated von Willebrand Factor and Factor VIII concentrate (Wilate).

Authors:  M Stadler; G Gruber; C Kannicht; L Biesert; K U Radomski; H Suhartono; K Pock; A Neisser-Svae; J Weinberger; J Römisch; T-E Svae
Journal:  Biologicals       Date:  2006-02-23       Impact factor: 1.856

6.  Phase II prospective open-label trial of recombinant interleukin-11 in desmopressin-unresponsive von Willebrand disease and mild or moderate haemophilia A.

Authors:  Margaret V Ragni; Enrico M Novelli; Anila Murshed; Elizabeth P Merricks; Mark T Kloos; Timothy C Nichols
Journal:  Thromb Haemost       Date:  2012-12-13       Impact factor: 5.249

7.  Treatment of von Willebrand disease with a high-purity factor VIII/von Willebrand factor concentrate: a prospective, multicenter study.

Authors:  Pier M Mannucci; Juan Chediak; Wahid Hanna; John Byrnes; Marlies Ledford; Bruce M Ewenstein; Anastassios D Retzios; Barbara A Kapelan; Richard S Schwartz; Craig Kessler
Journal:  Blood       Date:  2002-01-15       Impact factor: 22.113

8.  A comparative in vitro evaluation of six von Willebrand factor concentrates.

Authors:  S Lethagen; M Carlson; A Hillarp
Journal:  Haemophilia       Date:  2004-05       Impact factor: 4.287

9.  An influence of ABO blood group on the rate of proteolysis of von Willebrand factor by ADAMTS13.

Authors:  D J Bowen
Journal:  J Thromb Haemost       Date:  2003-01       Impact factor: 5.824

10.  A revised classification of von Willebrand disease. For the Subcommittee on von Willebrand Factor of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis.

Authors:  J E Sadler
Journal:  Thromb Haemost       Date:  1994-04       Impact factor: 5.249

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  5 in total

Review 1.  Rare forms of von Willebrand disease.

Authors:  Emmanuel J Favaloro
Journal:  Ann Transl Med       Date:  2018-09

2.  Von Willebrand disease type 2M: Correlation between genotype and phenotype.

Authors:  Dominique P M S M Maas; Ferdows Atiq; Nicole M A Blijlevens; Paul P T Brons; Sandy Krouwel; Britta A P Laros-van Gorkom; Frank W G Leebeek; Laurens Nieuwenhuizen; Selene C M Schoormans; Annet Simons; Daniëlle Meijer; Waander L van Heerde; Saskia E M Schols
Journal:  J Thromb Haemost       Date:  2021-11-21       Impact factor: 16.036

3.  Recombinant von Willebrand factor for severe gastrointestinal bleeding unresponsive to other treatments in a patient with type 2A von Willebrand disease: a case report.

Authors:  Racquel Brown
Journal:  Blood Coagul Fibrinolysis       Date:  2017-10       Impact factor: 1.276

Review 4.  Current and Emerging Options for the Management of Inherited von Willebrand Disease.

Authors:  Jessica M Heijdra; Marjon H Cnossen; Frank W G Leebeek
Journal:  Drugs       Date:  2017-09       Impact factor: 9.546

5.  Clinical Application of Factor VIII:C to VWF:Ag Ratio for the Screening of Haemophilia A Carriers.

Authors:  Ki-Young Yoo; Soo-Young Jung; Jin-Young Choi; Hye-Ryeon Park; Young-Shil Park
Journal:  J Clin Med       Date:  2022-03-18       Impact factor: 4.241

  5 in total

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