Using micrornas to control activation status of hepatic stellate cells and to prevent fibrosis in progressive liver diseases
View Patent ↗Provided herein are methods and compositions for treatment and/or prevention of liver disease. Aspects of the present disclosure relate to the engineering of a quiescent Hepatic Stellate Cell, and use of the engineered quiescent Hepatic Stellate Cell, or population thereof in the treatment and/or prevention of liver disease.
1. A method for treating or delaying progression of a disease associated with activated hepatic stellate cells (HSCs) in a subject, the method comprising in vivo administering to a subject who has, is suspected of having, or at risk of having a disease associated with activated HSCs a first composition comprising miR-412, a miR-412 mimic or a nucleic acid sequence encoding miR-412,
wherein the disease associated with activated hepatic stellate cells (HSCs) is selected from the group consisting of: liver fibrosis, alpha-1 antitrypsin deficiency, autoimmune hepatitis, biliary atresia, cirrhosis, nonalcoholic fatty liver disease (NAFLD), hepatic cancer, hepatic fibrosis, hepatic steatosis (fatty liver disease), Gilbert's syndrome, hemochromatosis, lysosomal acid lipase deficiency, primary biliary cholangitis, sarcoidosis, toxic hepatitis, tyrosinemia, viral hepatitis A, viral hepatitis B, viral hepatitis C, and Wilson disease.
2. The method of claim 1 , wherein the disease associated with activated HSCs is NAFLD or hepatotoxicity.
3. The method of claim 1 , wherein the first composition further comprises miR-15a, a miR-15a mimic or a nucleic acid sequence encoding miR-15a.
4. The method of claim 1 , further comprising, after administering, a step of administering a second composition comprising miR15a or nucleic acid encoding miR15a.
5. The method of claim 1 , wherein the first composition further comprises a pharmaceutically acceptable carrier.
6. The method of claim 1 , further comprising, prior to administering, a step of diagnosing the subject as having or at risk of having a disease associated with activated HSCs.
7. The method of claim 1 , wherein the administration is repeated at least once.
8. The method of claim 1 , wherein the subject is a mammal.
9. The method of claim 1 , wherein the subject is a human.
10. The method of claim 1 , wherein the first composition is administered via direct injection, intra-hepatic injection, i.v. administration, or parenteral administration.
11. A method for treating or delaying progression of a disease associated with activated HSCs in a subject, the method comprising in vivo administering to a subject who has, is suspected of having, or at risk of having a disease associated with activated HSCs a first composition comprising miR-15a, a miR-15a mimic or a nucleic acid sequence encoding miR-15a,
wherein the disease associated with activated hepatic stellate cells (HSCs) is selected from the group consisting of: liver fibrosis, alpha-1 antitrypsin deficiency, autoimmune hepatitis, biliary atresia, cirrhosis, nonalcoholic fatty liver disease (NAFLD), hepatic cancer, hepatic fibrosis, hepatic steatosis (fatty liver disease), Gilbert's syndrome, hemochromatosis, lysosomal acid lipase deficiency, primary biliary cholangitis, sarcoidosis, toxic hepatitis, tyrosinemia, viral hepatitis A, viral hepatitis B, viral hepatitis C, and Wilson disease.
12. The method of claim 11 , wherein the disease associated with activated HSCs is NAFLD or hepatotoxicity.
13. The method of claim 11 , further comprising, after administering, a step of administering a second composition comprising miR-412, a miR-412 mimic or a nucleic acid sequence encoding miR-412.
14. The method of claim 11 , wherein the first composition further comprises a pharmaceutically acceptable carrier.
15. A method for treating or delaying progression of a disease associated with activated HSCs in a subject, the method comprising in vivo administering to a subject who has, is suspected of having, or at risk of having a disease associated with activated HSCs
(a) a composition comprising miR-15a, a miR-15a mimic or a nucleic acid sequence encoding miR-15a, and
(b) a composition comprising miR-412, a miR-412 mimic or a nucleic acid sequence encoding miR-412,
wherein the disease associated with activated hepatic stellate cells (HSCs) is selected from the group consisting of: liver fibrosis, alpha-1 antitrypsin deficiency, autoimmune hepatitis, biliary atresia, cirrhosis, nonalcoholic fatty liver disease (NAFLD), hepatic cancer, hepatic fibrosis, hepatic steatosis (fatty liver disease), Gilbert's syndrome, hemochromatosis, lysosomal acid lipase deficiency, primary biliary cholangitis, sarcoidosis, toxic hepatitis, tyrosinemia, viral hepatitis A, viral hepatitis B, viral hepatitis C, and Wilson disease.
16. The method of claim 15 , wherein the composition of (a) is administered at substantially the same time as the composition of (b).