IP Library › Granted Patent US 6,878,371
Granted Patent B2
US 6,878,371 · App. 09/915,853 · Granted Apr 12, 2005

Therapeutic angiogenesis by bone marrow-derived cell transplantation in myocardial ischemic tissue and skeletal muscle ischemic tissue

Assignee: Boston Scientific Scimed, Inc.
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 6,878,371
App. No.
09/915,853
Granted
Apr 12, 2005
Kind
B2
Abstract

This invention provides methods of forming new blood vessels in diseased or damaged tissue in a subject, methods of increasing blood flow to diseased or damaged tissue in a subject, and methods of increasing angiogenesis in diseased tissue in a subject, which methods comprise: a) isolating autologous bone marrow-mononuclear cells from the subject; and b) transplanting locally into the diseased or damaged tissue an effective amount of the autologous bone-marrow mononuclear cells, thereby forming new blood vessels in the diseased or damaged tissue. The new blood vessels may be capillaries or collateral vessels in ischemic tissue or any site of angiogenesis. Also provided are methods of treating tissue in disease or injury by local transplantation with an effective amount of the autologous bone marrow-mononuclear cells so as to induce vascularization in such diseased tissue.

Claims (31)

1. A method of forming new blood vessels in cardiac muscle tissue in a subject, wherein the subject is a human, which comprises:

a) isolating autologous bone marrow-mononuclear cells from the human, wherein the autologous bone marrow-mononuclear cells are isolated from bone marrow; and

b) transplanting locally into the cardiac muscle tissue an effective amount of the autologous bone-marrow mononuclear cells, resulting in formation of new blood vessels in the cardiac muscle tissue.

2. The method of claim 1 , wherein the new blood vessels comprise capillaries.

3. The method of claim 1 , wherein the new blood vessels comprise collateral vessels.

4. The method of claim 1 , wherein the cardiac muscle tissue is ischemic cardiac muscle tissue.

5. The method of claim 1 , wherein the cardiac muscle tissue is damaged cardiac muscle tissue.

6. The method of claim 5 , wherein the damaged cardiac muscle tissue is an artificially created site.

7. A method of increasing blood flow to cardiac muscle tissue in a subject, wherein the subject is a human, which comprises:

a) isolating autologous bone-marrow mononuclear cells from the human, wherein the autologous bone marrow-mononuclear cells are isolated from bone marrow; and

b) transplanting locally into the cardiac muscle tissue an effective amount of the autologous bone-marrow mononuclear cells so as to result in formation of new blood vessels in the cardiac muscle tissue, thereby increasing the blood flow to the cardiac muscle tissue in the human.

8. The method of claim 7 , wherein the new blood vessels comprise capillaries.

9. The method of claim 7 , wherein the new blood vessels comprise collateral blood vessels.

10. The method of claim 7 , wherein the cardiac muscle tissue is ischemic cardiac muscle tissue.

11. The method of claim 7 , wherein the cardiac muscle tissue is damaged cardiac muscle tissue.

12. The method of claim 11 , wherein the damaged cardiac muscle tissue is an artificially created site.

13. A method of treating diseased cardiac muscle tissue in a subject, wherein the subject is a human, which comprises:

a) isolating autologous bone-marrow mononuclear cells from the human, wherein the autologous bone marrow-mononuclear cells are isolated from bone marrow; and

b) transplanting locally into the diseased cardiac muscle tissue an effective amount of the autologous bone-marrow mononuclear cells so as to result in formation of new blood vessels, thereby treating the diseased cardiac muscle tissue in the human.

14. The method of claim 13 , wherein the diseased cardiac muscle tissue is ischemic cardiac muscle tissue.

15. The method of claim 13 , wherein the new blood vessels comprise capillaries.

16. The method of claim 13 , wherein the new blood vessels comprise collateral blood vessels.

17. A method of increasing angiogenesis in diseased cardiac muscle tissue in a subject, wherein the subject is a human, which comprises:

a) isolating autologous bone-marrow mononuclear cells from the human, wherein the autologous bone marrow-mononuclear cells are isolated from bone marrow; and

b) transplanting locally into the diseased cardiac muscle tissue an effective amount of the autologous bone-marrow mononuclear cells, thereby increasing angiogenesis in the diseased cardiac muscle tissue in the human.

18. The method of claim 17 , wherein the diseased cardiac muscle tissue is ischemic cardiac muscle tissue.

19. A method of treating heart failure in a mammal, wherein the subject is a human, which comprises:

a) isolating autologous bone-marrow mononuclear cells from the human, wherein the autologous bone marrow-mononuclear cells are isolated from bone marrow; and

b) transplanting locally into the heart an effective amount of the autologous bone-marrow mononuclear cells so as to result in formation of new blood vessels, thereby treating heart failure in the human.

20. The method of claim 19 , wherein the new blood vessels comprise capillaries.

21. The method of claim 19 , wherein the new blood vessels comprise collateral blood vessels.

Assignments (2)
MERGER Recorded Feb 17, 2005
From: SCIMED LIFE SYSTEMS, INC.
To: BOSTON SCIENTIFIC SCIMED, INC.
Reel/Frame 015737/0536 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 30, 2004
From: UENO, TAKAFUMI; MUROHARA, TOYOAKI; ROBINSON, KEITH ALLEN; CHRONOS, NICOLAS A.F.; BALDWIN, SAM; PALASIS, MARIA
To: SCIMED LIFE SYSTEMS, INC.
Reel/Frame 014635/0591 →
Continuity (2)
Provisional Application 6022083400 · Jul 26, 2000
Related Publication 20020037278A1 · Mar 28, 2002