Pancreatic endocrine progenitor cell therapies for the treatment of obesity and type 2 diabetes (T2D)
Provided herein are therapies, and methods using that therapy, in the treatment of one or more of Type 2 diabetes (T2D), obesity, glucose intolerance and insulin resistance or to control weight gain in subjects. In particular, the subject may be candidates for treatment with one or more small molecule anti-diabetic drugs and the therapy may include implanting a population of pancreatic endocrine progenitor cells into the subject, where the cells are allowed to mature in vivo to produce a population.
1. A method for treating obesity, glucose intolerance or insulin resistance in a subject with type 2 diabetes (T2D), the method comprising: implanting a population of pancreatic endocrine progenitor cells into the subject, wherein the pancreatic endocrine progenitor cells mature in vivo to produce a population comprising pancreatic endocrine cells.
2. The method of claim 1 , the method further comprising administering a therapeutically effective amount of one or more small molecule anti-diabetic drugs to the subject.
3. The method of claim 1 , wherein the pancreatic endocrine progenitor cells mature in vivo to produce a population comprising at least 2% pancreatic endocrine cells.
4. The method of claim 2 , wherein the one or more small molecule anti-diabetic drugs are selected from the following: meglitinides; sulfonylureas; dipeptidyl-peptidase 4 (DPP-4) inhibitors; biguanides; thiazolidinediones; alpha-glucosidase inhibitors; sodium-glucose transporter 2 (SGLT-2) inhibitors; and bile acid sequestrants.
5. The method of claim 2 , wherein the small molecule anti-diabetic drug is selected from the group consisting of: repaglinide; nateglinide; glipizide; glimepiride; glyburide; saxagliptin; sitagliptin; linagliptin; metformin; rosiglitazone; pioglitazone; acarbose; miglitol; canagliflozin; dapagliflozin; empagliflozin; and colsevelam.
6. The method of claim 2 , wherein the anti-diabetic drug is selected from the group consisting of: sitagliptin; metformin; and rosiglitazone.
7. The method of claim 1 , wherein the method comprises treating glucose intolerance in the subject.
8. The method of claim 1 , wherein the method comprises treating insulin resistance in the subject.
9. A method for treating obesity, glucose intolerance or insulin resistance in a subject with type 2 diabetes (T2D), the method comprising:
implanting a population of pancreatic endocrine progenitor cells into the subject, wherein the pancreatic endocrine progenitor cells mature in vivo to produce a population comprising pancreatic endocrine cells; and
administering to the subject a therapeutically effective amount of one or more of sitagliptin; metformin; and rosiglitazone.
10. The method of claim 9 , wherein the pancreatic endocrine progenitor cells mature in vivo to produce a population comprising at least 2% pancreatic endocrine cells.
11. The method of claim 9 , wherein the method comprises treating obesity in the subject.
12. The method of claim 9 , wherein the method comprises treating glucose intolerance in the subject.
13. The method of claim 9 , wherein the method comprises treating insulin resistance in the subject.
14. A method for treating obesity, glucose intolerance or insulin resistance in a subject with type 2 diabetes (T2D) to whom a therapeutically effective amount of an anti-diabetic drug has been administered, the method comprising:
implanting a population of pancreatic endocrine progenitor cells into the subject wherein the pancreatic endocrine progenitor cells mature in vivo to produce a population comprising pancreatic endocrine cells;
wherein the anti-diabetic drug is sitagliptin, metformin, or rosiglitazone.
15. The method of claim 14 , wherein the pancreatic endocrine progenitor cells mature in vivo to produce a population comprising at least 2% pancreatic endocrine cells.
16. The method of claim 14 , wherein the method comprises treating obesity in the subject.
17. The method of claim 14 , wherein the method comprises treating glucose intolerance in the subject.
18. The method of claim 14 , wherein the method comprises treating insulin resistance in the subject.