The important role of von Willebrand factor in platelet‐derived FVIII gene therapy for murine hemophilia A in the presence of inhibitory antibodies. (11th June 2015)

• Record Type: Journal Article
• Authors: Shi, Q.; Schroeder, J. A.; Kuether, E. L.; Montgomery, R. R.
• Is Part Of: Journal of thrombosis and haemostasis. Volume 13:Number 7(2015:Jul.)
• Page Start: 1301
• Page End: 1309
• Publication Date: 2015-06-11
• Subjects: Thrombosis -- Periodicals; Hemostasis -- Periodicals; Blood coagulation disorders -- Periodicals; 616.1
• DOI: 10.1111/jth.13001
• Languages: English
• ISSNs: 1538-7933

Abstract

<abstract abstract-type="main" id="jth13001-abs-0001"> <title>Summary</title> <sec id="jth13001-sec-0001" sec-type="section"> <title>Background</title> <p>Our previous studies have demonstrated that targeting FVIII expression to platelets results in FVIII storage together with von Willebrand factor (VWF) in platelet α‐granules and that platelet‐derived FVIII (2bF8) corrects the murine hemophilia A phenotype even in the presence of high‐titer anti‐FVIII inhibitory antibodies (inhibitors).</p> </sec> <sec id="jth13001-sec-0002" sec-type="section"> <title>Objective</title> <p>To explore how VWF has an impact on platelet gene therapy for hemophilia A with inhibitors.</p> </sec> <sec id="jth13001-sec-0003" sec-type="section"> <title>Methods</title> <p>2bF8 transgenic mice in the FVIII<sup>−/−</sup> background (2bF8<sup>tg+/−</sup>F8<sup>−/−</sup>) with varying VWF phenotypes were used in this study. Animals were analyzed by VWF ELISA, FVIII activity assay, Bethesda assay and tail clip survival test.</p> </sec> <sec id="jth13001-sec-0004" sec-type="section"> <title>Results</title> <p>Only 18% of 2bF8<sup>tg+/−</sup>F8<sup>−/−</sup>VWF<sup>−/−</sup> animals, in which VWF was deficient, survived the tail clip challenge with inhibitor titers of 3–8000 BU mL<sup>−1</sup>. In contrast, 82% of 2bF8<sup>tg+/−</sup>F8<sup>−/−</sup>VWF<sup>+/+</sup> mice, which had normal VWF levels, survived tail clipping with inhibitor titers of 10–50 000 BU mL<sup>−1</sup>. All 2bF8<sup>tg+/−</sup>F8<sup>−/−</sup>VWF<sup>−/−</sup> mice without inhibitors survived tail clipping and no VWF<sup>−/−</sup>F8<sup>−/−</sup> mice survived this challenge. Because VWF is synthesized by endothelial cells and megakaryocytes and is distributed in both plasma and platelets in peripheral blood, we further investigated the effect of each compartment of VWF on platelet‐FVIII gene therapy for hemophilia A with inhibitors. In the presence of inhibitors, 42% of animals survived tail clipping in the group with plasma‐VWF and 50% survived in the platelet‐VWF group.</p> </sec> <sec id="jth13001-sec-0005" sec-type="section"> <title>Conclusion</title> <p>VWF is essential for platelet gene therapy for hemophilia A with inhibitors. Both platelet‐VWF and plasma‐VWF are required for optimal platelet‐derived FVIII gene therapy for hemophilia A in the presence of inhibitors.</p> </sec> </abstract>