IP Library Granted Patent US 10,376,545
Granted Patent B2
US 10,376,545 · App. 15/478,094 · Granted Aug 13, 2019

Methods for producing hormone secreting cells in a subject

Inventors: Alan D. Agulnick (San Diego, CA); Kevin Allen D'Amour (San Diego, CA)
Assignee: ViaCyte, Inc.
A61K35/39A61K35/545C12N5/0676C12N5/0678C12N2500/25C12N2501/115C12N2501/117C12N2501/119C12N2501/15C12N2501/155C12N2501/16C12N2501/195C12N2501/385C12N2501/415C12N2501/727C12N2501/998C12N2501/999C12N2506/02C12N2506/45C12N2533/90
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Quick Facts
Patent No.
US 10,376,545
App. No.
15/478,094
Granted
Aug 13, 2019
Kind
B2
Abstract

A human immature endocrine cell population and methods for making an immature endocrine cell population are provided. Specifically, immature beta cells and methods for production of immature beta cells are described. Immature beta cells co-express INS and NKX6.1 and are uni-potent and thereby develop into mature beta cells when implanted in vivo. The mature beta cells in vivo are capable of producing insulin in response to glucose stimulation.

Claims (21)

1. A method for producing hormone secreting cells, said method comprising:

maturing transplanted endocrine cells in vivo in a subject wherein the endocrine cells co-express INS+ and NKX6.1+, thereby producing hormone secreting cells.

2. The method of claim 1 , wherein the endocrine cells are CHGA+.

3. The method of claim 1 , wherein the hormone secreting cells secrete insulin and glucagon.

4. The method of claim 1 , wherein the subject is a mammalian subject.

5. The method of claim 4 , wherein the mammalian subject is a human subject.

6. The method of claim 5 , wherein the human subject has been identified as having a condition which limits the ability of the subject to produce sufficient levels of insulin in response to physiologically high blood glucose concentrations.

7. The method of claim 1 , further comprising detecting insulin secretion, wherein insulin secretion is detected by measuring C-peptide levels in a subject into whom the endocrine cells have been transplanted.

8. The method of claim 7 , wherein C-peptide levels in the subject increase over time.

9. The method of claim 1 , wherein the hormone secreting cells are insulin secreting cells that are responsive to blood glucose.

10. The method of claim 1 , wherein the number of hormone-secreting cells increases over time.

11. The method of claim 1 , wherein the hormone secreting cells are insulin secreting cells that form islet-like cell clusters.

12. The method of claim 1 , wherein the endocrine cells are unipotent.

13. The method of claim 1 , wherein the endocrine cells are aggregates.

14. The method of claim 13 , wherein the aggregates are 50 to 300 microns in diameter.

15. The method of claim 1 , wherein the endocrine cells are in a semipermeable encapsulation device.

16. The method of claim 1 , wherein the endocrine cells do not substantially express NGN3.

17. A method for producing hormone secreting cells, said method comprising:

maturing transplanted human cells in vivo, wherein the transplanted human cells comprise unipotent human immature beta cell suspension aggregates and wherein at least 10% of cells in the beta cell suspension aggregates are human immature beta cells that co-express INS and NKX6.1,

thereby producing hormone secreting cells.

18. The method of claim 17 , wherein the hormone secreting cells secrete insulin.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 30, 2019
From: D'AMOUR, KEVIN
To: VIACYTE, INC.
Reel/Frame 049038/0399 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 18, 2017
From: AGULNICK, ALAN D.
To: VIACYTE, INC.
Reel/Frame 043612/0290 →
Continuity (4)
Continuation 14455059 · Aug 8, 2014
Continuation 14106330 · Dec 13, 2013
Provisional Application 61781005 · Mar 14, 2013
Related Publication 20170202885A1 · Jul 20, 2017