2011 Fiscal Year Final Research Report
Establishment of novel cellular therapy for hemophilia A using autologous blood outgrowth endothelial progenitors
Project/Area Number |
22790995
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Single-year Grants |
Research Field |
Pediatrics
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Research Institution | Nara Medical University |
Principal Investigator |
MATSUI Hideto 奈良県立医科大学, 医学部, 講師 (00571027)
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Project Period (FY) |
2010 – 2011
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Keywords | 小児血液学 |
Research Abstract |
We have established ex vivo gene transfer system using genetically-modified blood outgrowth endothelial progenitor cells(BOECs) which are capable of synthesizing therapeutic levels of plasma FVIII over a prolonged time periods.^<20> Using this ex vivo gene transfer strategy, we can provide for the safe and efficacious delivery of FVIII following subcutaneous implantation of BOECs in hemophilia A mouse model. Now, we would like to try this strategy in hemophilia A dog model.
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[Journal Article] A microRNA-regulated and GP64-pseudotyped lentiviral vectors mediated stable expression of FVIII in murine model of hemophilia A2011
Author(s)
Matsui H, Hegadorn C, Ozelo M, Burnett E, Tuttle A, Labelle A, McCray PB Jr, Naldini L, Brown B, Hough C, Lillicrap D
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Journal Title
Molecular Therapy
Volume: 19(4)
Pages: 723-730
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