Neonatal gene transfer leads to widespread correction of pathology in a murine model of lysosomal storage disease.

Abstract

For many inborn errors of metabolism, early treatment is critical to prevent long-term developmental sequelae. We have used a gene-therapy approach to demonstrate this concept in a murine model of mucopolysaccharidosis type VII (MPS VII). Newborn MPS VII mice received a single intravenous injection with 5.4 x 10(6) infectious units of recombinant adeno-associated virus encoding the human beta-glucuronidase (GUSB) cDNA. Therapeutic levels of GUSB expression were achieved by 1 week of age in liver, heart, lung, spleen, kidney, brain, and retina. GUSB expression persisted in most organs for the 16-week duration of the study at levels sufficient to either reduce or prevent completely lysosomal storage. Of particular significance, neurons, microglia, and meninges of the central nervous system were virtually cleared of disease. In addition, neonatal treatment of MPS VII mice provided access to the central nervous system via an intravenous route, avoiding a more invasive procedure later in life. These data suggest that gene transfer mediated by adeno-associated virus can achieve therapeutically relevant levels of enzyme very early in life and that the rapid growth and differentiation of tissues does not limit long-term expression.

• Authors: T M Daly, C Vogler, B Levy, M E Haskins, M S Sands
• Journal: Proceedings of the National Academy of Sciences of the United States of America (Proc Natl Acad Sci U S A) Vol. 96 Issue 5 Pg. 2296-300 (Mar 02 1999) ISSN: 0027-8424 [Print] United States
• PMID: 10051635 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)

Chemical References

• DNA, Complementary
• Glycosaminoglycans
• Recombinant Proteins
• Glucuronidase

Topics

• Animals
• Animals, Newborn
• DNA, Complementary
• Dependovirus
• Gene Transfer Techniques
• Genetic Therapy
• Genetic Vectors
• Glucuronidase (biosynthesis, genetics)
• Glycosaminoglycans (metabolism)
• Humans
• Liver (metabolism, pathology)
• Lysosomal Storage Diseases (pathology, therapy)
• Lysosomes (enzymology)
• Mice
• Mice, Mutant Strains
• Mucopolysaccharidosis VII (metabolism, pathology, therapy)
• Polymerase Chain Reaction
• Recombinant Proteins (biosynthesis)