Hepatocyte based insulin gene therapy for diabetes
AssigneeWisconsin Alumni Research Foundation
InventorsTausif Alam, Hans Sollinger
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AssigneeWisconsin Alumni Research Foundation
InventorsTausif Alam, Hans Sollinger
Estimating the term…
A method and vectors for controlling blood glucose levels in a mammal are disclosed. In one embodiment, the method comprises the steps of: treating the hepatocyte cells of a patient with a first, second or third vector, wherein the first vector comprises a promoter enhancer, glucose inducible regulatory elements, a liver-specific promoter, a gene encoding human insulin with modified peptidase and an albumin 3′UTR and lacks an HGH intron, wherein the second vector comprises an HGH intron, glucose inducible regulatory elements, a liver-specific promoter, a gene encoding human insulin with modified peptidase site and an albumin 3′UTR and lacks a promoter enhancer, wherein the third vector comprises an HGH intron, glucose inducible regulatory elements, a liver-specific promoter, a gene encoding human insulin with modified peptidase site, an albumin 3′UTR and a promoter enhancer and observing the patient's insulin levels, wherein the patient's insulin levels are controlled.
A method for obtaining glucose-regulated expression of insulin ex vivo in mammalian hepatocytes, wherein the method comprises delivering a first, second or third genetic vector for glucose-regulated synthesis of insulin into an isolated mammalian hepatocyte and wherein the insulin levels in the blood of the mammal stays within 0.5 uU-100 uU/ml and the blood glucose concentration of the mammal stays within 80-150 mg/dl for at least 10 days after transplant of the mammalian hepatocytes into a mammal,
A vector suitable for controlling blood glucose levels in a mammal,
A method of controlling blood glucose levels in a mammal, comprising the steps of:
Dependencies are inferred from the claim text.