| Literature DB >> 1370472 |
J M Wilson1, M Grossman, C H Wu, N R Chowdhury, G Y Wu, J R Chowdhury.
Abstract
Familial hypercholesterolemia is an inherited disease in humans, caused by a deficiency of low density lipoprotein (LDL) receptors, that we have used as a model for developing liver-directed gene therapies. Our strategy is to reconstitute hepatic LDL receptor expression in vivo by administering a DNA-protein complex that is capable of targeting the delivery of functional LDL receptor genes to hepatocytes. Infusion of this DNA-protein complex into the peripheral circulation of a rabbit animal model for familial hypercholesterolemia resulted in hepatocyte-specific gene transfer and a temporary amelioration of hypercholesterolemia. This noninvasive approach to gene therapy should have applications in the treatment of a wide spectrum of human diseases.Entities:
Mesh:
Substances:
Year: 1992 PMID: 1370472
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157