IP Library Granted Patent US 10,071,121
Granted Patent B2
US 10,071,121 · App. 14/940,057 · Granted Sep 11, 2018

Cardiac, mesenchymal and endothelial progenitor cell (CPC) chimeras and methods for making and using them

Inventors: Mark A. Sussman (San Diego, CA); Pearl J. Quijada (San Diego, CA)
Assignee: SAN DIEGO STATE UNIVERSITY (SDSU) FOUNDATION
A61K35/34A61K35/28A61K35/44C12N5/0657C12N5/0668C12N5/16C12N2510/00
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Quick Facts
Patent No.
US 10,071,121
App. No.
14/940,057
Granted
Sep 11, 2018
Kind
B2
Abstract

In alternative embodiments, provided are chimeric cells, which in alternative embodiments are the so-called “cardiochimeras”, and methods for making and using them. In alternative embodiments, exemplary chimeric cells as provided herein comprise a cardiac stem cell of cardiac origin or a cardiac progenitor cell fused to either a mesenchymal progenitor cell or mesenchymal stem cell, an endothelial progenitor cell or endothelial stem cell, or a cardiac stem cell or a cardiac progenitor cell. In alternative embodiments, the chimeric cells as provided herein comprise an endothelial progenitor cell, which may or may not be of cardiac origin, fused to either a mesenchymal progenitor cell or mesenchymal stem cell, an endothelial progenitor cell or endothelial stem cell, or a cardiac stem cell or a cardiac progenitor cell. In alternative embodiments, methods for making chimeric cells as provided herein further comprise selecting a cell fusion product comprising a viable chimera of the fused cells. In alternative embodiments, methods for making chimeric cells as provided herein comprise use of any known cell fusion technique, for example, using a Sendai virus, such as a Sendai virus Hemagglutinating Virus of Japan Envelope (HVJ-E), a polyethylene glycol, liposomes or lipids, a fusion protein, electrofusion and/or equivalents thereof. In alternative embodiments, provided are cell lines, chimera (chimeric) cell lines or chromosomally-stable chimera cell lines, derived or made from chimeric cells as provided herein. In alternative embodiments, provided are methods for inducing cardiogenesis in a mammalian heart comprising administration to an individual in need thereof (for example, a human), chimeric cells as provided herein, or a cell line, a chimera cell line or a chromosomally-stable chimera as provided herein. In alternative embodiments, provided are methods for treating or ameliorating a heart injury, a congenital or genetic heart defect, or a heart dysfunction, comprising administration to an individual in need thereof (for example, a human), chimeric cells as provided herein, or a cell line, a chimera cell line or a chromosomally-stable chimera as provided herein.

Claims (56)

1. A method for making a chimeric cell, comprising:

(a)

(i) providing a first cell, wherein the first cell comprises:

a cardiac stem cell of cardiac origin;

(ii) providing a second cell, wherein the second cell comprises:

(1) a mesenchymal progenitor cell or mesenchymal stem cell; or

(2) an endothelial progenitor cell or endothelial stem cell;

(iii) inducing fusion between the first cell and the second cell, thereby generating a cell fusion product.

2. The method of claim 1 , further comprising clonally expanding the cell fusion product.

3. The method of claim 1 , wherein the fusion is induced using a method comprising use of a cell fusion technique selected from the group consisting of: a Sendai virus or Hemagglutinating Virus of Japan Envelope (HVJ-E); a polyethylene glycol; liposomes or lipids; a fusion protein; and electrofusion.

4. The method of claim 1 , wherein:

the second cell is an endothelial progenitor cell or an endothelial stem cell.

5. The method of claim 1 , wherein the first cell and the second cell are each a mammalian cell.

6. A cell fusion product or a viable chimera, produced by a method of claim 1 .

7. A chromosomally-stable chimera cell line, produced by a method of claim 1 .

8. A cell fusion product comprising: a fusion product of:

a first cell comprising

a cardiac progenitor cell (CPC);

and

a second cell comprising a stem cell or a progenitor cell.

9. The cell fusion product of claim 8 , wherein said second cell comprises:

(a) a mesenchymal stem cell of cardiac origin or non-cardiac origin;

(b) an endothelial progenitor cell of cardiac origin or non-cardiac origin; or

(c) a cardiac stem cell or a cardiac progenitor cell.

10. The cell fusion product of claim 8 , wherein

the second cell is a cardiac stem cell of cardiac origin.

11. A product of manufacture comprising a chimeric cell made by a method of claim 1 ,

in combination with a delivery device suitable for delivering the chimeric cell to cardiac tissue.

12. The product of manufacture of claim 11 ,

wherein the delivery device is an implant, a catheter, a stent, a gel, a hydrogel, a chitosan-based hydrogel, a biocompatible scaffold, or a biomimetic support.

13. A method for inducing cardiogenesis in a mammalian heart, comprising:

(a) providing a cell or a plurality of cells made by a method of claim 1 , and

(b) introducing the cell or cells of (a) to a mammalian heart, thereby inducing cardiogenesis in the mammalian heart.

14. The method of claim 13 ,

wherein the mammalian heart has an injury, a congenital defect, a genetic defect, or a dysfunction, and the method is effective to treat the injury, defect or the dysfunction.

15. A method for inducing cardiogenesis in a mammalian heart, comprising:

(a) providing a product of manufacture of claim 11 , and

(b) introducing the product of manufacture of (a) to a mammalian heart, thereby inducing cardiogenesis in the mammalian heart.

16. A method for treating or ameliorating a heart injury subsequent to a myocardial infarction (MI), a congenital or genetic heart defect, or a heart dysfunction, comprising:

(a) providing a cell or a plurality of cells made by a method of claim 1 , and

(b) administering the cell or cells of (a) to a heart of an individual in need thereof,

thereby treating or ameliorating the heart injury subsequent to a myocardial infarction (MI), congenital or genetic heart defect, or heart dysfunction or heart failure.

17. A method for treating or ameliorating a heart injury subsequent to a myocardial infarction (MI), a congenital or genetic heart defect, or a heart dysfunction, comprising:

(a) providing a cell fusion product of claim 8 , and

(b) administering the cell fusion product of (a) to a heart of an individual in need thereof,

thereby treating or ameliorating the heart injury subsequent to a myocardial infarction (MI), congenital or genetic heart defect, or heart dysfunction or heart failure.

18. A method for treating or ameliorating a heart injury subsequent to a myocardial infarction (MI), a congenital or genetic heart defect, or a heart dysfunction, comprising:

(a) providing a product of manufacture of claim 11 , and

(b) administering the product of manufacture of (a) to a heart of an individual in need thereof,

thereby treating or ameliorating the heart injury subsequent to a myocardial infarction (MI), congenital or genetic heart defect, or heart dysfunction or heart failure.

19. The method of claim 1 , further comprising selecting a cell fusion product comprising a viable chimera of the first and the second cell.

20. The method of claim 2 , further comprising selecting a chimera cell line on the basis of enhanced cardiogenic potential, reduced immunogenic potential, or both enhanced cardiogenic potential and reduced immunogenic potential.

21. The method of claim 5 , wherein the cell fusion is a human cell to human cell fusion, a human cell to non-human cell fusion, or a non-human cell to a non-human cell fusion, or the cell fusion is a human, or a murine, a rodent, a rat or a mouse cell fusion product, or a murine to murine cell fusion product.

22. The product of manufacture of claim 11 , fabricated as an implant, a catheter, a stent, or a medical device, or wherein the chimeric cell is formulated with or mixed with or within a gel, a hydrogel, a chitosan-based hydrogel, a biocompatible scaffold, or a biomimetic support.

23. The product of manufacture of claim 14 , wherein the injury, defect or dysfunction is a myocardial infarction (MI), an ischemic injury, a heart failure, or results from a myocardial infarction (MI).

24. The method of claim 15 , wherein the mammalian heart has an injury, a congenital or genetic defect, or a dysfunction, and the method is effective to treat the injury, defect or the dysfunction, or the injury, defect or dysfunction is a myocardial infarction (MI), an ischemic injury, a heart failure, or results from a myocardial infarction (MI).

Assignments (1)
CONFIRMATORY LICENSE Recorded Nov 19, 2015
From: SAN DIEGO STATE UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 037146/0508 →
Continuity (2)
Provisional Application 62080110 · Nov 14, 2014
Related Publication 20160346330A1 · Dec 1, 2016