Literature DB >> 25955153

The important role of von Willebrand factor in platelet-derived FVIII gene therapy for murine hemophilia A in the presence of inhibitory antibodies.

Q Shi1,2,3,4, J A Schroeder1,2,3, E L Kuether1,2,3, R R Montgomery1,2,3.   

Abstract

BACKGROUND: 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).
OBJECTIVE: To explore how VWF has an impact on platelet gene therapy for hemophilia A with inhibitors.
METHODS: 2bF8 transgenic mice in the FVIII(-/-) background (2bF8(tg+/-) F8(-/-) ) 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.
RESULTS: Only 18% of 2bF8(tg+/-) F8(-/-) VWF(-/-) animals, in which VWF was deficient, survived the tail clip challenge with inhibitor titers of 3-8000 BU mL(-1) . In contrast, 82% of 2bF8(tg+/-) F8(-/-) VWF(+/+) mice, which had normal VWF levels, survived tail clipping with inhibitor titers of 10-50,000 BU mL(-1) . All 2bF8(tg+/-) F8(-/-) VWF(-/-) mice without inhibitors survived tail clipping and no VWF(-/-) F8(-/-) 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.
CONCLUSION: 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.
© 2015 International Society on Thrombosis and Haemostasis.

Entities:  

Keywords:  gene therapy; hemophilia A; neutralizing antibody; platelet; von Willebrand factor

Mesh:

Substances:

Year:  2015        PMID: 25955153      PMCID: PMC4496307          DOI: 10.1111/jth.13001

Source DB:  PubMed          Journal:  J Thromb Haemost        ISSN: 1538-7836            Impact factor:   5.824


  46 in total

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  8 in total

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3.  Induction of activated T follicular helper cells is critical for anti-FVIII inhibitor development in hemophilia A mice.

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Review 5.  Platelet-Targeted Gene Therapy for Hemophilia.

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Journal:  Mol Ther Methods Clin Dev       Date:  2018-02-07       Impact factor: 6.698

Review 6.  Platelet-Targeted FVIII Gene Therapy Restores Hemostasis and Induces Immune Tolerance for Hemophilia A.

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Journal:  Front Immunol       Date:  2020-06-12       Impact factor: 7.561

7.  A novel mouse model of type 2N VWD was developed by CRISPR/Cas9 gene editing and recapitulates human type 2N VWD.

Authors:  Qizhen Shi; Scot A Fahs; Jeremy G Mattson; Hongyin Yu; Crystal L Perry; Patricia A Morateck; Jocelyn A Schroeder; Jessica Rapten; Hartmut Weiler; Robert R Montgomery
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8.  The severe spontaneous bleeding phenotype in a novel hemophilia A rat model is rescued by platelet FVIII expression.

Authors:  Qizhen Shi; Jeremy G Mattson; Scot A Fahs; Aron M Geurts; Hartmut Weiler; Robert R Montgomery
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  8 in total

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