This program at the University of Minnesota is focused on gene therapy for metabolic disorders causing mental retardation. Toward this goal, the program currently has one clinical gene therapy protocol before the FDA to treat Hunter syndrome (mucopolysaccharidosis type II, iduronate-2- sulfatase deficiency) and is pursuing approval of clinical-grade retrovirus vector L2SN and the scale-up methods for ex vivo lymphocyte gene therapy. The program will develop clinically applicable large-scale methods to isolate, transduce and for cryopreservation of lymphocytes and hematopoietic stem cells (HSC) from bone marrow, peripheral blood and umbilical cord blood. In addition, it plans to improve recombinant enzyme delivery, potentially across the blood-brain barrier, by studying HSC transduction to treat Hurler syndrome(a-L-iduronidase deficiency) and by developing a new adeno-associated virus (AAV) based gene delivery vehicle appropriate for non-mitotic cells. The program also aims to develop a practical approach to treat the devastating neurologic insults of acute neonatal hyperammonemia associated with ornithine transcarbamylase (OTC) deficiency, carbamyl phosphate synthetase (CPS) deficiency and by other genetic and acquired forms of liver failure. By genetically engineering E. coli to serve as an enteric ammonia trap, bacteria simultaneously expressing OCT and CPS would utilize the natural enteric dialysis system to lower high levels of ammonia. The program is complemented by multiple units offering institutional resources and support including the Institute of Human Genetics, Minnesota Center for Disabilities Research on Developmental Disabilities, the University of Minnesota, Bone Marrow Transplantation Program, the Cancer Center and the Clinical Research Center. By the end of the five year grant period, this program intends to have developed and initiated clinical trials for multiple metabolic disorders causing mental retardation, a challenging but feasible goal which is particularly fitting for the end of 'the decade of the brain.'

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Program Projects (P01)
Project #
5P01HD032652-05
Application #
2857456
Study Section
Special Emphasis Panel (SRC (GT))
Program Officer
Hanson, James W
Project Start
1995-01-10
Project End
1999-12-31
Budget Start
1999-01-01
Budget End
1999-12-31
Support Year
5
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of Minnesota Twin Cities
Department
Pediatrics
Type
Schools of Medicine
DUNS #
168559177
City
Minneapolis
State
MN
Country
United States
Zip Code
55455
Ou, Li; Przybilla, Michael J; Whitley, Chester B (2018) Metabolomics profiling reveals profound metabolic impairments in mice and patients with Sandhoff disease. Mol Genet Metab :
Ou, L; Przybilla, M J; Whitley, C B (2018) SAAMP 2.0: An algorithm to predict genotype-phenotype correlation of lysosomal storage diseases. Clin Genet 93:1008-1014
Ou, Li; Przybilla, Michael J; Whitley, Chester B (2017) Phenotype prediction for mucopolysaccharidosis type I by in silico analysis. Orphanet J Rare Dis 12:125
Hyland, Kendra A; Aronovich, Elena L; Olson, Erik R et al. (2017) Transgene Expression in Dogs After Liver-Directed Hydrodynamic Delivery of Sleeping Beauty Transposons Using Balloon Catheters. Hum Gene Ther 28:541-550
Aronovich, Elena L; Hyland, Kendra A; Hall, Bryan C et al. (2017) Prolonged Expression of Secreted Enzymes in Dogs After Liver-Directed Delivery of Sleeping Beauty Transposons: Implications for Non-Viral Gene Therapy of Systemic Disease. Hum Gene Ther 28:551-564
Ou, Li; Przybilla, Michael J; Whitley, Chester B (2017) Proteomic analysis of mucopolysaccharidosis I mouse brain with two-dimensional polyacrylamide gel electrophoresis. Mol Genet Metab 120:101-110
Verhaart, Ingrid E C; Robertson, Agata; Wilson, Ian J et al. (2017) Prevalence, incidence and carrier frequency of 5q-linked spinal muscular atrophy - a literature review. Orphanet J Rare Dis 12:124
Ou, Li; Przybilla, Michael J; Koniar, Brenda L et al. (2016) Elements of lentiviral vector design toward gene therapy for treating mucopolysaccharidosis I. Mol Genet Metab Rep 8:87-93
Aronovich, Elena L; Hackett, Perry B (2015) Lysosomal storage disease: gene therapy on both sides of the blood-brain barrier. Mol Genet Metab 114:83-93
Satzer, David; DiBartolomeo, Christina; Ritchie, Michael M et al. (2015) Assessment of dysmyelination with RAFFn MRI: application to murine MPS I. PLoS One 10:e0116788

Showing the most recent 10 out of 92 publications