Cardiac muscle repair or regeneration using bone marrow-derived stem cells
View Patent ↗Disclosed are compositions and methods for method of treating a subject having reduced cardiac function or cardiac disease by administering adult bone marrow-derived stem cells to an individual. In some embodiments, the subject is a myocardial infarction patient or congestive heart failure patient. These cells can be administered as a liquid injectable or as a preparation of cells in a matrix which is or becomes solid or semi-solid. The cells can be genetically modified to enhance myocardial differentiation and integration. Also disclosed is a method for replacing cells ex vivo in a heart valve for implantation.
1. A method of treating a subject having reduced cardiac function or a cardiac disease comprising the step of: administering to the subject allogeneic bone marrow-derived stem cells, in an amount effective for the bone marrow-derived stem cells to engraft to the subject's heart and promote myogenesis.
2. The method of claim 1 , wherein the method comprises treating a subject having myocardial infarction.
3. The method of claim 1 , wherein the subject is selected from the group consisting of ischemic heart transplant patient and coronary artery bypass graft patient.
4. The method of claim 1 , wherein myogenesis comprises morphological changes consistent with myogenesis in the bone marrow derived stem cells.
5. The method of claim 1 , wherein the bone marrow-derived cells express at least one muscle specific protein.
6. The method of claim 1 , wherein the bone marrow-derived stem cells are administered intraarterially.
7. The method of claim 2 , wherein the myocardial infarction involves about 5 percent to about 40 percent of muscle mass of the left ventricle.
8. The method of claim 2 , wherein the myocardial infarction involves about 20 percent of muscle mass of the left ventricle.
9. The method of claim 1 , wherein the bone marrow-derived cells stem cells are administered in a pharmaceutically acceptable liquid carrier.
10. The method of claim 9 , wherein the pharmaceutically acceptable liquid carrier comprises phosphate buffer saline.
11. The method of claim 1 , wherein the bone marrow-derived stem cells are administered in a suspension containing about 10×10 6 to about 40×10 6 bone marrow-derived stem cells per ml.
12. The method of claim 11 , wherein the suspension is administered in an amount of about 20 μl to about 150 ml.
13. The method of claim 1 , wherein the subject is a human.