In this R21 grant application, we propose here to study gene delivery to inhibit HIV replication and HIV toxicity for CNS cells. HIV encephalopathy is a common and potentially devastating complication of AIDS. Development of HW encephalopathy largely reflects HIV infection of brain cells, especially monocyte-derived macrophages (MDM) and microglia. It also may involve toxicity of certain HIV proteins for neurons. We will use gene delivery techniques to study inhibition of H1V infection and replication in primary cultured human MDM and microglia, and to examine protection of neurons from the ability of HIV gp120 envelope glycoprotein to induce apoptosis. Recombinant gene delivery vehicles derived from Talphag-deleted SV40 (rSV40s) permanently transduce unselected key CNS targets for HW, including microglia, neurons, and monocyte-derived macrophages (MDM) with >98% efficiency in vitro. We have found that HIV replicates in MDM and microglia, and that rSV40s carrying HIV inhibitory transgenes protect these cells from HIV replication. We have found as well that gp120 causes apoptosis in cultured neurons, and that rSV40 vectors that downregulate cell membrane CXCR4 or that provide antioxidant enzymes, such as catalase, protect these neurons. We propose to exploit these promising findings to study rSV40 gene delivery to protect the CNS cells from HIV. This proposal is based on the following hypothesis: To test this hypothesis, we propose the following specific aims: 1.) Identify optimal transgenes individually and in combination to inhibit HIV-1 in CNS cells. 2.) use gene delivery to protect NT2-derived neurons from apoptosis induced by HIV gene products. Despite the frequency and dire consequences of CNS HIV infection, people afflicted with HIV encephalopathy have few treatment options. We propose to address this therapeutic challenge using rSV40 gene delivery to the CNS, both to protect the brain from HIV infection and to mitigate HIV-induced CNS dysfunction.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Exploratory/Developmental Grants (R21)
Project #
5R21MH069122-02
Application #
6800556
Study Section
Special Emphasis Panel (ZRG1-AARR-5 (04))
Program Officer
Bao, Jing
Project Start
2003-09-15
Project End
2006-08-31
Budget Start
2004-09-01
Budget End
2006-08-31
Support Year
2
Fiscal Year
2004
Total Cost
$157,000
Indirect Cost
Name
Thomas Jefferson University
Department
Pathology
Type
Schools of Medicine
DUNS #
053284659
City
Philadelphia
State
PA
Country
United States
Zip Code
19107
Louboutin, J-P; Agrawal, L; Reyes, B A S et al. (2012) Gene delivery of antioxidant enzymes inhibits human immunodeficiency virus type 1 gp120-induced expression of caspases. Neuroscience 214:68-77
Louboutin, Jean-Pierre; Strayer, David S (2012) Blood-brain barrier abnormalities caused by HIV-1 gp120: mechanistic and therapeutic implications. ScientificWorldJournal 2012:482575
Louboutin, J-P; Reyes, B A S; Agrawal, L et al. (2012) Intracisternal rSV40 administration provides effective pan-CNS transgene expression. Gene Ther 19:114-8
Louboutin, Jean-Pierre; Reyes, Beverly A S; Agrawal, Lokesh et al. (2010) Blood-brain barrier abnormalities caused by exposure to HIV-1 gp120--protection by gene delivery of antioxidant enzymes. Neurobiol Dis 38:313-25
Strayer, David S; Mitchell, Christine; Maier, Dawn A et al. (2010) Production of SV40-derived vectors. Cold Spring Harb Protoc 2010:pdb.prot5436
Strayer, David S; Mitchell, Christine; Maier, Dawn A et al. (2010) Titering replication-defective rSV40 vectors. Cold Spring Harb Protoc 2010:pdb.prot5437
Louboutin, Jean-Pierre; Agrawal, Lokesh; Reyes, Beverly A S et al. (2010) HIV-1 gp120-induced injury to the blood-brain barrier: role of metalloproteinases 2 and 9 and relationship to oxidative stress. J Neuropathol Exp Neurol 69:801-16
Louboutin, Jean-Pierre; Agrawal, Lokesh; Reyes, Beverly A S et al. (2009) A rat model of human immunodeficiency virus 1 encephalopathy using envelope glycoprotein gp120 expression delivered by SV40 vectors. J Neuropathol Exp Neurol 68:456-73
Louboutin, Jean-Pierre; Agrawal, Lokesh; Liu, Bianling et al. (2008) In vivo gene transfer to the CNS using recombinant SV40-derived vectors. Expert Opin Biol Ther 8:1319-35
Louboutin, J-P; Agrawal, L; Reyes, B A S et al. (2007) Protecting neurons from HIV-1 gp120-induced oxidant stress using both localized intracerebral and generalized intraventricular administration of antioxidant enzymes delivered by SV40-derived vectors. Gene Ther 14:1650-61

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