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Ex vivo gene therapy of familial hypercholesterolemia
J M Wilson1, M Grossman, S E Raper
1Division of Molecular Medicine and Genetics, University of Michigan Medical School.
Insights
Gene therapy using corrected autologous hepatocytes lowered cholesterol in Watanabe Heritable Hyperlipidemic rabbits, a model for familial hypercholesterolemia. This approach offers potential for treating severe genetic lipid disorders.
Area of Science:
- Genetics
- Cardiovascular Science
- Hepatology
Background:
- Familial hypercholesterolemia (FH) is a genetic disorder causing high LDL cholesterol and premature heart disease.
- Standard treatments are ineffective for homozygous FH patients with minimal LDL receptor activity.
- Liver transplantation has shown success but is invasive.
Purpose of the Study:
- To develop and evaluate gene therapy for homozygous familial hypercholesterolemia (FH).
- To utilize the Watanabe Heritable Hyperlipidemic (WHHL) rabbit model for preclinical studies.
Main Methods:
- Primary hepatocytes were isolated from WHHL rabbits.
- A functional LDL receptor gene was introduced into hepatocytes using retroviral vectors.
- Genetically corrected autologous hepatocytes were transplanted back into the rabbits.
Main Results:
- Transplantation of corrected hepatocytes led to a 30-40% sustained decrease in serum cholesterol.
- Functional LDL receptor RNA was detected in the liver for at least 6 months.
- No apparent immunological response to the gene-corrected cells was observed.
Conclusions:
- Autologous transplantation of gene-corrected hepatocytes is a promising strategy for FH.
- This gene therapy approach effectively reduces cholesterol levels in a relevant animal model.
- Further research may lead to new treatments for severe genetic hypercholesterolemia.
Abstract:
Familial hypercholesterolemia (FH) is an autosomal dominant disorder caused by a deficiency in the receptor that clears low density lipoprotein (LDL) from the serum (reviewed in Ref. 1 and 2). Patients with one abnormal LDL receptor allele have moderate elevations in plasma LDL and suffer premature coronary artery disease (CAD). Approximately 5% of all patients under 45 who have had a myocardial infarction carry this trait. Patients with two abnormal LDL receptor genes (homozygous deficient patients) have severe hypercholesterolemia and life-threatening coronary artery disease in childhood. Strategies for treating patients with FH are directed at lowering the plasma level of LDL. In heterozygotes, this is accomplished through the administration of drugs that stimulate the expression of LDL receptor from the normal allele (2). This therapeutic approach is not effective in the treatment of homozygous deficient patients, especially those that retain less than 2% of residual LDL receptor activity. Partial amelioration of hyperlipidemia has been achieved in some homozygous deficient patients by diverting the portal circulation through a portacaval anastomosis (3) and by chronic plasmapheresis therapy (4). A more direct approach has been to correct the deficiency of hepatic LDL receptor by transplanting a liver that expresses normal levels of LDL receptor. Three patients that survived this procedure normalized their serum LDL-cholesterol (5-9). We have used an authentic animal model for FH, the Watanabe Heritable Hyperlipidemic rabbit (WHHL), to develop gene therapies for the homozygous form of FH (10-13). The WHHL rabbit has a mutation in its LDL receptor gene which renders the receptor completely dysfunctional (12) leading to severe hypercholesterolemia, diffuse atherosclerosis, and premature death. The potential efficacy of gene therapy for FH is supported by a series of studies we have performed in the WHHL rabbit in which we have achieved metabolic improvement (14-18). Liver tissue was removed from WHHL rabbits and used to isolate hepatocytes and establish primary cultures. A functional rabbit LDL receptor gene was transduced into a high proportion of hepatocytes using recombinant retroviruses, and the genetically corrected cells were transplanted into the animal from which they were derived. Transplantation of the genetically corrected, autologous hepatocytes was associated with a 30-40% decrease in serum cholesterol that persisted for the duration of the experiment (4 months, Ref. 18). Recombinant derived LDL receptor RNA was detected in liver for at least 6 months. There was no apparent immunological response to the recombinant derived LDL receptor.(ABSTRACT TRUNCATED AT 400 WORDS)