One of the characteristics of vector administration into the CNS is the ability of the transgene products and/or viral particles to travel along neural pathways. In our preliminary experiments in monkeys where the AAV-2 vector was administered into the striatum, transgene product was detected in afferent and efferent regions including the internal and external portion of the globus pallidus, subthalamic nucleus, substantia nigra reticulata and compacta, thalamus and cortex at 3 or 8 weeks after gene delivery. This strongly indicates that both retrograde and anterograde transport of vector and transgene product must be carefully evaluated as it may impact therapeutic applications of gene transfer. As the PDGTSG has identified rAAV and lentviral vectors as the initial two most promising vectors (see Principal Projects I and II) these will be the focus of this Pipeline Project. To address this transport issue this project will systematically analyze the axonal transport characteristics of AAV-2, the alternative serotype AAV-5 and lentiviral vectors in monkeys following intrastriatal administration. Each vector type will be delivered unilaterally into the striatum of normal monkeys and resulting gene expression and presence of the gene product will be detected at the site of gene delivery and projection sites. Fuorophore-labelled viral particles will be delivered in the contralateral striatum and detected at 48 hours later at the injection site and the projection regions. Results of this project will lead to an understanding of patterns of distribution of each of the viral vectors and will provide critical information regarding final design of Principal Projects.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Specialized Center--Cooperative Agreements (U54)
Project #
1U54NS045309-01
Application #
6690920
Study Section
Special Emphasis Panel (ZNS1-SRB-E (02))
Project Start
2002-09-30
Project End
2007-08-31
Budget Start
Budget End
2003-08-31
Support Year
1
Fiscal Year
2002
Total Cost
$163,636
Indirect Cost
Name
University of Rochester
Department
Type
DUNS #
208469486
City
Rochester
State
NY
Country
United States
Zip Code
14627
Bankiewicz, Krystof S; Sudhakar, Vivek; Samaranch, Lluis et al. (2016) AAV viral vector delivery to the brain by shape-conforming MR-guided infusions. J Control Release 240:434-442
Mineharu, Yohei; Castro, Maria G; Lowenstein, Pedro R et al. (2013) Dendritic cell-based immunotherapy for glioma: multiple regimens and implications in clinical trials. Neurol Med Chir (Tokyo) 53:741-54
Kells, Adrian P; Forsayeth, John; Bankiewicz, Krystof S (2012) Glial-derived neurotrophic factor gene transfer for Parkinson's disease: anterograde distribution of AAV2 vectors in the primate brain. Neurobiol Dis 48:228-35
Mittermeyer, Gabriele; Christine, Chadwick W; Rosenbluth, Kathryn H et al. (2012) Long-term evaluation of a phase 1 study of AADC gene therapy for Parkinson's disease. Hum Gene Ther 23:377-81
Gimenez, Francisco; Krauze, Michal T; Valles, Francisco et al. (2011) Image-guided convection-enhanced delivery of GDNF protein into monkey putamen. Neuroimage 54 Suppl 1:S189-95
Fiandaca, Massimo S; Salegio, Ernesto Aguilar; Yin, Dali et al. (2011) Human/nonhuman primate AC-PC ratio--considerations for translational brain measurements. J Neurosci Methods 196:124-30
Philippidou, Polyxeni; Valdez, Gregorio; Akmentin, Wendy et al. (2011) Trk retrograde signaling requires persistent, Pincher-directed endosomes. Proc Natl Acad Sci U S A 108:852-7
Yin, Dali; Valles, Francisco E; Fiandaca, Massimo S et al. (2011) Optimal region of the putamen for image-guided convection-enhanced delivery of therapeutics in human and non-human primates. Neuroimage 54 Suppl 1:S196-203
Yang, J; Sanderson, N S R; Wawrowsky, K et al. (2010) Kupfer-type immunological synapse characteristics do not predict anti-brain tumor cytolytic T-cell function in vivo. Proc Natl Acad Sci U S A 107:4716-21
de Silva, S; Mastrangelo, M A; Lotta Jr, L T et al. (2010) Extending the transposable payload limit of Sleeping Beauty (SB) using the Herpes Simplex Virus (HSV)/SB amplicon-vector platform. Gene Ther 17:424-31

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