PROJECT 3: PONCZ Program Director/Principal Investigator (Last, First. Middle): High. Katherine A. PROJECT 3: PLATELET FACTOR 8 AS A NOVEL THERAPY FOR HEMOPHILIA A Names and titles of investigator(s): ? IVIortimer Poncz, M.D. Professor of Pediatrics, University of Pennsylvania. The Children's Hospital of Philadelphia. ? Rodney Camire, Ph.D. Associate Professor of Pediatrics, University of Pennsylvania. The Children's Hospital of Philadelphia. Description of Project 3 Hemophilia A is the most common inherited severe bleeding diathesis and is due to a deficiency/dysfunction of coagulation Factor Vlll (F8). Replacement therapy is effective for bleeding episodes, but is expensive and remains associated with bleeding sequelae. Importantly, up to 30% of these patients develop antibodies that inhibit F8 activity. Strategies to treat bleeding complications in this subgroup of patients can be problematic, especially if immunotherapy/tolerance to eliminate the inhibitor is unsuccessful. We were the first to describe the ability of ectopically expressed B-domainless human (/?) F8 in platelets (p/7BF8) to be effective at correcting the bleeding diathesis in F8-deficient (F8"""""""""""""""""""""""") mice. We also showed that phBF8 is 100-fold more effective than plasma hFQ in the face of circulating inhibitors. These advantages of phF8 are tempered by our observation that the resulting clots in p/?BF8/F8"""""""""""""""""""""""" mice are less stable than clots formed in F8"""""""""""""""" mice after /7F8 infusions and embolize more easily. We therefore believe that phF8 may have clinical utility, but needs enhanced efficacy to improve its hemostatic function. There are 3 specific aims to this proposal:
Specific Aim 1 : Understand and improve clot formation in pF8/F8"""""""""""""""""""""""" mice. We now present new findings since the prior submission that pF8 variants that increase specific activity and/or reduce the apoptotic effect of pF8 on megakaryopoiesis and/or increase pF8 expression levels can markedly improve hemostatic outcome in F8"""""""""""""""""""""""" mice. Proposed studies will confirm these distinct processes and identify strong pF8 candidates to be tested in both a large animal F8"""""""""""""""""""""""" model and in a human-mouse xenotransplant model as described below.
Specific Aim 2 : Large animal studies of pFS. The most effective pF8 variants defined in Specific Aim 1 will be studied using a lentiviral-based pF8 expression system to drive expression in the megakaryocytes of a canine F8"""""""""""""""" model as a prelude to human studies. These canine studies will examine efficacy in improving spontaneous bleeding episodes and in bleeding models, including cuticular and FeCIa arterial and venous injury models, in these F8"""""""""""""""" dogs.
Specific Aim 3 : Studies of pF8 in human hematopoietic cells. To address whether our lentiviral strategy will work in human hematopoietic cells, we propose to also examine lentiviral-delivery of the best pF8s into (3D34* human hematopoietic cells and demonstrate that we can achieve similar levels of F8 in human as in murine megakaryocytes and that the pF8 localizes within a-granules. Immune-compromised mice will also be reconstituted with these progenitor cells, and the level of F8 antigen and activity that can be achieved in platelets in these xenotransplanted mice measured. In summary, our prior studies have demonstrated that pF8 offers a novel therapeutic strategy for the care of patients with hemophilia A, especially for those patients with problematic circulating inhibitors, but this approach may also be associated with increased clot instability and embolization. The proposed studies will further analyze the features of F8 that can effect pF8 hemostatic efficacy in murine studies and carry these concepts and pF8 variants forward to large animal and pre-clinical human-mouse xenotransplant studies. PHS 398 (Rev. 06/09) Page Continuation Format Page 166 PROJECT 3: Poncz Principal Investigator/Program Director (Last, First, Middle): High, Katherine A. FROM THROUGH DETAILED BUDGET FOR INITIAL BUDGET PERIOD DIRECT COSTS ONLY

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
2P01HL064190-11A1
Application #
8185324
Study Section
Heart, Lung, and Blood Initial Review Group (HLBP)
Project Start
2011-07-01
Project End
2016-06-30
Budget Start
2011-08-05
Budget End
2012-06-30
Support Year
11
Fiscal Year
2011
Total Cost
$371,335
Indirect Cost
Name
Children's Hospital of Philadelphia
Department
Type
DUNS #
073757627
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
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Sim, Xiuli; Poncz, Mortimer; Gadue, Paul et al. (2016) Understanding platelet generation from megakaryocytes: implications for in vitro-derived platelets. Blood 127:1227-33
Arruda, V R; Samelson-Jones, B J (2016) Gene therapy for immune tolerance induction in hemophilia with inhibitors. J Thromb Haemost 14:1121-34
Marcos-Contreras, Oscar A; Smith, Shannon M; Bellinger, Dwight A et al. (2016) Sustained correction of FVII deficiency in dogs using AAV-mediated expression of zymogen FVII. Blood 127:565-71
Siner, Joshua I; Samelson-Jones, Benjamin J; Crudele, Julie M et al. (2016) Circumventing furin enhances factor VIII biological activity and ameliorates bleeding phenotypes in hemophilia models. JCI Insight 1:e89371
High, Katherine A; Anguela, Xavier M (2016) Adeno-associated viral vectors for the treatment of hemophilia. Hum Mol Genet 25:R36-41
Zhang, Nanyan; Zhi, Huiying; Curtis, Brian R et al. (2016) CRISPR/Cas9-mediated conversion of human platelet alloantigen allotypes. Blood 127:675-80
Lyde, R; Sabatino, D; Sullivan, S K et al. (2015) Platelet-delivered therapeutics. J Thromb Haemost 13 Suppl 1:S143-50
Wang, Yuhuan; Hayes, Vincent; Jarocha, Danuta et al. (2015) Comparative analysis of human ex vivo-generated platelets vs megakaryocyte-generated platelets in mice: a cautionary tale. Blood 125:3627-36
Arruda, Valder R; Samelson-Jones, Ben J (2015) Obstacles and future of gene therapy for hemophilia. Expert Opin Orphan Drugs 3:997-1010

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