Large Animal Model for Evaluating the Efficacy of the Gene Therapy in Ischemic Heart

10.3791/62833 ◽  
2021 ◽  
Author(s):  
Henna Korpela ◽  
Satu Siimes ◽  
Seppo Ylä-Herttuala
Keyword(s):  
Gene Therapy ◽  
Animal Model ◽  
Ischemic Heart ◽  
Large Animal Model ◽  
Large Animal

scholarly journals Cardiac AAV9-S100A1 Gene Therapy Rescues Post-Ischemic Heart Failure in a Preclinical Large Animal Model

2011 ◽  
Vol 3 (92) ◽  
pp. 92ra64-92ra64 ◽  
Author(s):  
S. T. Pleger ◽  
C. Shan ◽  
J. Ksienzyk ◽  
R. Bekeredjian ◽  
P. Boekstegers ◽  
...  
Keyword(s):  
Heart Failure ◽  
Gene Therapy ◽  
Animal Model ◽  
Ischemic Heart ◽  
Large Animal Model ◽  
Large Animal ◽  
Ischemic Heart Failure

scholarly journals 197Inhibition of TASK-1 by gene therapy and pharmacological compounds suppresses atrial fibrillation in a large animal model

2018 ◽  
Vol 39 (suppl_1) ◽  
Author(s):  
C Schmidt ◽  
F Wiedmann ◽  
C Beyersdorf ◽  
Z Zhao ◽  
I El-Battrawy ◽  
...  
Keyword(s):  
Atrial Fibrillation ◽  
Gene Therapy ◽  
Animal Model ◽  
Large Animal Model ◽  
Large Animal

scholarly journals Inducible scAAV2.GRE.MMP1 lowers IOP long-term in a large animal model for steroid-induced glaucoma gene therapy

Gene Therapy ◽  
2016 ◽  
Vol 23 (5) ◽  
pp. 438-449 ◽  
Author(s):  
T Borrás ◽  
L K Buie ◽  
M G Spiga
Keyword(s):  
Gene Therapy ◽  
Animal Model ◽  
Large Animal Model ◽  
Large Animal

Development of a Novel Large Animal Model of Ischemic Heart Failure Using Autologous Platelet Aggregates

2010 ◽  
Vol 33 (2) ◽  
pp. 63-71 ◽  
Author(s):  
Pawel Kwiatkowski ◽  
Chittoor Sai-Sudhakar ◽  
Angela Philips ◽  
Sampath Parthasarathy ◽  
Benjamin Sun
Keyword(s):  
Heart Failure ◽  
Animal Model ◽  
Ischemic Heart ◽  
Large Animal Model ◽  
Large Animal ◽  
Ischemic Heart Failure ◽  
Platelet Aggregates ◽  
Autologous Platelet

Effective gene therapy for an inherited CNS disease in a large animal model

2005 ◽  
Vol 57 (3) ◽  
pp. 355-364 ◽  
Author(s):  
Charles H. Vite ◽  
Joseph C. McGowan ◽  
Sumit N. Niogi ◽  
Marco A. Passini ◽  
Kenneth J. Drobatz ◽  
...  
Keyword(s):  
Gene Therapy ◽  
Animal Model ◽  
Large Animal Model ◽  
Large Animal ◽  
Cns Disease

scholarly journals Gene Therapy in a Large Animal Model of PDE6A-Retinitis Pigmentosa

2017 ◽  
Vol 11 ◽  
Author(s):  
Freya M. Mowat ◽  
Laurence M. Occelli ◽  
Joshua T. Bartoe ◽  
Kristen J. Gervais ◽  
Ashlee R. Bruewer ◽  
...  
Keyword(s):  
Gene Therapy ◽  
Animal Model ◽  
Retinitis Pigmentosa ◽  
Large Animal Model ◽  
Large Animal

Platelet-Targeted Expression of Coagulation Factor VIII (FVIII) Shows Efficacy for Using the Dog as a Large Animal Model for Gene Therapy of Hemophilia a

Blood ◽  
2008 ◽  
Vol 112 (11) ◽  
pp. 3525-3525 ◽  
Author(s):  
David A. Wilcox ◽  
Lily M. Du ◽  
Sandra L. Haberichter ◽  
Paula M. Jacobi ◽  
Juan Fang ◽  
...  
Keyword(s):  
Gene Therapy ◽  
Bone Marrow ◽  
Animal Model ◽  
Whole Blood ◽  
Hemophilia A ◽  
Active Form ◽  
Biologically Active ◽  
Large Animal Model ◽  
Sublethal Dose ◽  
Large Animal

Abstract In order to develop a large animal model for platelet-targeted gene therapy of Hemophilia A, we transduced normal canine bone marrow with a lentivirus vector under the transcriptional control of integrin αIIb gene promoter driving expression of human BDD-FVIII. Bone marrow was collected from normal dogs and transduced in the presence of recombinant canine c-SCF, c-IL-6, human h-TPO, and h-flt-3/flk-2 ligand differentiation factor. Immunofluorescence analysis using antibodies against human FVIII, and the megakaryocyte-specific marker integrin αIIb revealed synthesis of FVIII within tissue cultured megakaryocytes derived from lentivirus transduced bone marrow cells. This result appeared similar to synthesis, trafficking and storage of FVIII trafficked to α-granules of the murine “small animal” model for hemophilia A and human megakaryoyctes in vitro. To examine the effect of FVIII expression in platelets, in vivo, FVIII-transduced canine bone marrow was xenotransplanted into immune-compromised “NOD-SCID” mice treated with a sublethal dose (350 cGy) of irradiation. Flow cytometric analysis using antibodies specific for canine glycoproteins Ibα and integrin αIibβ3 revealed that circulating canine platelets comprised approximately 20–30% of the total platelet population in whole blood isolated from the mice within four weeks after xenotransplant. Immunofluorescence confocal microscopy detected a punctuate staining for FVIII that co-localized with a platelet α–granule protein, P-selectin, within a subpopulation of canine platelets isolated from murine whole blood. In contrast, FVIII was not detected in platelets from control samples. In addition, chromogenic analysis of platelets isolated from mice transplanted with FVIII-transduced bone marrow demonstrated the presence of a biologically active form of FVIII, FVIII:C at 2 mU/ml/lysate of 1×108 platelets. These results indicate that canine megakaryocytes are able to synthesize and store a biologically active form of FVIII that can be retained within progeny platelets. We speculate that dogs affected with hemophilia A should serve as an ideal “large animal” model to test if FVIII can undergo regulated release from platelets following physiologic hemostatic response to vessel injury. This raises the possibility of developing a locally inducible secretory pool of FVIII in platelets of patients with Hemophilia A following autologous transplantation of FVIII-transduced hematopoietic stem cells.

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