IP Library Granted Patent US 9,597,395
Granted Patent B2
US 9,597,395 · App. 11/138,083 · Granted Mar 21, 2017

Methods of using adipose tissue-derived cells in the treatment of cardiovascular conditions

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Quick Facts
Patent No.
US 9,597,395
App. No.
11/138,083
Granted
Mar 21, 2017
Kind
B2
Abstract

Adipose derived regenerative cells are used to treat patients, including patients with cardiovascular conditions, diseases or disorders. Methods of treating patients include processing adipose tissue to deliver a concentrated amount of regenerative cells, e.g., stem and/or progenitor cells, obtained from the adipose tissue to a patient. The methods may be practiced in a closed system so that the stem cells are not exposed to an external environment prior to being administered to a patient. Accordingly, in a preferred method, adipose derived regenerative cells are placed directly into a recipient along with such additives necessary to promote, engender or support a therapeutic cardiovascular benefit.

Claims (67)

1. A method of improving cardiac ejection fraction in a subject, comprising:

identifying a subject in need of improved cardiac ejection fraction; and

providing to the subject a composition comprising a concentrated population of adipose-derived regenerative cells sufficient to improve cardiac ejection fraction in said subject, wherein said concentrated population of adipose-derived regenerative cells comprises adipose-derived stem cells and endothelial progenitor cells, and wherein said concentrated population of adipose-derived regenerative cells is obtained by acquiring an adipose tissue sample, separating away adipocytes and connective tissue, and washing and concentrating said adipose-derived regenerative cells.

2. The method of claim 1 , wherein the subject is human.

3. The method of claim 1 , wherein said concentrated population of adipose-derived regenerative cells comprises precursor cells.

4. The method of claim 1 , wherein said composition is provided to said subject in a bolus.

5. The method of claim 1 , wherein said composition is provided to said subject in multiple doses.

6. The method of claim 1 , wherein the composition is provided to said subject via at least one of an endomyocardial, epimyocardial, intraventricular, intracoronary, retrograde coronary sinus, intra-arterial, intra-pericardial, or intravenous administration route.

7. A method of improving cardiac perfusion in a subject, comprising:

identifying a subject with insufficient cardiac perfusion; and

providing to the subject a composition that comprises an amount of a concentrated population of adipose-derived regenerative cells sufficient to improve cardiac perfusion in said subject, wherein said concentrated population of adipose-derived regenerative cells comprises stem cells and endothelial progenitor cells, and wherein said concentrated population of adipose-derived regenerative cells is obtained by acquiring an adipose tissue sample, separating away adipocytes and connective tissue, and washing and concentrating said adipose-derived regenerative cells.

8. The method of claim 7 , wherein the subject is human.

9. The method of claim 7 , wherein said concentrated population of adipose-derived regenerative cells comprises precursor cells.

10. The method of claim 7 , wherein said composition is provided to said subject in a bolus.

11. The method of claim 7 , wherein said composition is provided to said subject in multiple doses.

12. The method of claim 7 , wherein the composition is provided to said subject via at least one of an endomyocardial, epimyocardial, intraventricular, intracoronary, retrograde coronary sinus, intra-arterial, intra-pericardial, or intravenous administration route.

13. A method for preventing the progression of cardiac remodeling in a subject, comprising:

identifying a subject at risk of cardiac remodeling; and

providing to the subject an amount of a composition comprising a concentrated population of adipose-derived regenerative cells is sufficient to prevent the progression of cardiac remodeling in said subject, wherein said concentrated population of adipose-derived regenerative cells comprises stem cells and endothelial progenitor cells, and wherein said concentrated population of adipose-derived regenerative cells is obtained by acquiring an adipose tissue sample, separating away adipocytes and connective tissue, and washing and concentrating said adipose-derived regenerative cells.

14. The method of claim 13 , wherein the subject is human.

15. The method of claim 13 , wherein said concentrated population of adipose-derived regenerative cells comprises precursor cells.

16. The method of claim 13 , wherein said composition is provided to said subject in a bolus.

17. The method of claim 13 , wherein said composition is provided to said subject in multiple doses.

18. The method of claim 13 , wherein the composition is provided to said subject via at least one of an endomyocardial, epimyocardial, intraventricular, intracoronary, retrograde coronary sinus, intra-arterial, intra-pericardial, or intravenous administration route.

19. The method of claim 1 , wherein said concentrated population of adipose-derived regenerative cells is isolated in a closed system.

20. The method of claim 7 , wherein said concentrated population of adipose-derived regenerative cells is isolated in a closed system.

21. The method of claim 13 , wherein said concentrated population of adipose-derived regenerative cells is isolated in a closed system.

22. The method of claim 1 , wherein said concentrated population of adipose-derived regenerative cells is not cultured.

23. The method of claim 7 , wherein said concentrated population of adipose-derived regenerative cells is not cultured.

24. The method of claim 13 , wherein said concentrated population of adipose-derived regenerative cells is not cultured.

25. The method of claim 19 , wherein said concentrated population of adipose-derived regenerative cells is not cultured.

26. The method of claim 20 , wherein said concentrated population of adipose-derived regenerative cells is not cultured.

27. The method of claim 21 , wherein said concentrated population of adipose-derived regenerative cells is not cultured.

28. The method of claim 1 , wherein said concentrated population of adipose-derived regenerative cells further comprises an additive.

29. The method of claim 28 , wherein said additive is selected from the group consisting of a disaggregation agent, an immunosuppressive agent, a growth factor, a tissue or cell re-aggregation inhibitor, and a scaffold, or any combination thereof.

30. The method of claim 7 , wherein said concentrated population of adipose-derived regenerative cells further comprises an additive.

31. The method of claim 30 , wherein said additive is selected from the group consisting of a disaggregation agent, an immunosuppressive agent, a growth factor, a tissue or cell re-aggregation inhibitor, and a scaffold, or any combination thereof.

32. The method of claim 13 , wherein said concentrated population of adipose-derived regenerative cells further comprises an additive.

33. The method of claim 32 , wherein said additive is selected from the group consisting of a disaggregation agent, an immunosuppressive agent, a growth factor, a tissue or cell re-aggregation inhibitor, and a scaffold, or any combination thereof.

34. The method of claim 1 , wherein said step of providing to the subject a composition comprising a concentrated population of adipose-derived regenerative cells improves exercise tolerance in said subject.

35. The method of claim 34 , wherein the subject is human.

36. The method of claim 34 , wherein the concentrated population of adipose-derived regenerative cells comprises precursor cells.

37. The method of claim 34 , wherein the composition is provided to said subject in a bolus.

38. The method of claim 34 , wherein the composition is provided to said subject in multiple doses.

39. The method of claim 34 , wherein the composition is provided to said subject via at least one of an endomyocardial, epimyocardial, intraventricular, intracoronary, retrograde coronary sinus, intra-arterial, intra-pericardial, or intravenous administration route.

40. The method of claim 34 , wherein said concentrated population of adipose-derived regenerative cells is isolated in a closed system.

41. The method of claim 34 , wherein said concentrated population of adipose-derived regenerative cells is not cultured.

42. The method of claim 40 , wherein said concentrated population of adipose-derived regenerative cells is not cultured.

43. The method of claim 34 , wherein said concentrated population of adipose-derived regenerative cells further comprises an additive.

44. The method of claim 43 , wherein said additive is selected from the group consisting of a disaggregation agent, an immunosuppressive agent, a growth factor, a tissue or cell re-aggregation inhibitor, and a scaffold, or any combination thereof.

45. The method of claim 1 , wherein said subject has acute myocardial infarction.

46. The method of claim 1 , wherein said subject has ischemic heart disease.

47. The method of claim 7 , wherein said subject has acute myocardial infarction.

48. The method of claim 7 , wherein said subject has ischemic heart disease.

49. The method of claim 13 , wherein said subject has acute myocardial infarction.

50. The method of claim 13 , wherein said subject has ischemic heart disease.

51. The method of claim 1 , wherein the composition provides a minimum concentration of 5.5×10 4 adipose-derived cells.

52. The method of claim 7 , wherein the composition provides a minimum concentration of 5.5×10 4 adipose-derived cells.

53. The method of claim 13 , wherein the composition provides a minimum concentration of 5.5×10 4 adipose-derived cells.

54. The method of claim 1 , wherein the frequency of stem cells in the concentrated population of adipose-derived regenerative cells is at least 0.1%.

55. The method of claim 7 , wherein the frequency of stem cells in the concentrated population of adipose-derived regenerative cells is at least 0.1%.

56. The method of claim 13 , wherein the frequency of stem cells in the concentrated population of adipose-derived regenerative cells is at least 0.1%.

57. The method of claim 7 , wherein said step of providing to the subject a composition comprising a concentrated population of adipose-derived regenerative cells improves exercise tolerance in said subject.

58. The method of claim 13 , wherein said step of providing to the subject a concentrated composition comprising a population of adipose-derived regenerative cells improves exercise tolerance in said subject.

59. The method of claim 1 , wherein said concentrated population of adipose-derived regenerative cells is cryopreserved.

60. The method of claim 7 , wherein said concentrated population of adipose-derived regenerative cells is cryopreserved.

61. The method of claim 13 , wherein said concentrated population of adipose-derived regenerative cells is cryopreserved.

Assignments (10)
CORRECTIVE ASSIGNMENT TO CORRECT THE CORRECT ASSIGNEE'S ADDRESS PREVIOUSLY RECORDED AT REEL: 049313 FRAME: 0434. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Aug 1, 2019
From: CYTORI THERAPEUTICS, INC.
To: LOREM VASCULAR PTE. LTD.
Reel/Frame 049942/0204 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 17, 2019
From: CYTORI THERAPEUTICS, INC.
To: LOREM VASCULAR PTE. LTD.
Reel/Frame 049313/0434 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 25, 2019
From: CYTORI THERAPEUTICS, INC.
To: LOREM VASCULAR PTE. LTD.
Reel/Frame 049651/0001 →
RELEASE OF SECURITY INTEREST Recorded Apr 25, 2019
From: OXFORD FINANCE LLC
To: CYTORI THERAPEUTICS, INC.
Reel/Frame 049011/0347 →
SECURITY INTEREST Recorded Sep 22, 2017
From: CYTORI THERAPEUTICS, INC.
To: OXFORD FINANCE LLC, AS COLLATERAL AGENT
Reel/Frame 043952/0150 →
RELEASE OF SECURITY INTEREST Recorded Jun 12, 2015
From: OXFORD FINANCE LLC
To: CYTORI THERAPEUTICS, INC.
Reel/Frame 035902/0191 →
RELEASE OF SECURITY INTEREST Recorded Jul 3, 2013
From: GENERAL ELECTRIC CAPITAL CORPORATION
To: CYTORI THERAPEUTICS, INC.
Reel/Frame 030734/0778 →
SECURITY AGREEMENT Recorded Jun 28, 2013
From: CYTORI THERAPEUTICS, INC.
To: OXFORD FINANCE LLC
Reel/Frame 030715/0625 →
SECURITY AGREEMENT Recorded Dec 3, 2012
From: CYTORI THERAPEUTICS INC.
To: GENERAL ELECTRIC CAPITAL CORPORATION
Reel/Frame 029395/0660 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 3, 2007
From: FRASER, JOHN K.; HEDRICK, MARC H.; ZHU, MIN; STREM, BRIAN M.; DANIELS, ERIC; WULUR, ISABELLA
To: CYTORI THERAPEUTICS, INC.
Reel/Frame 019650/0201 →