IP Library Granted Patent US 9,801,713
Granted Patent B2
US 9,801,713 · App. 14/987,601 · Granted Oct 31, 2017

Production of tissue engineered heart valves

Inventors: Anthony Atala (Winston-Salem, NC); James Yoo (Winston-Salem, NC)
Assignee: Wake Forest University Health
A61F2/2415A61L27/3604A61L27/3641A61L27/383A61L27/3808A61L27/3826A61L27/3839A61L27/3886A61L27/507B82Y5/00B82Y10/00C12N5/0068C12N5/069C12N2533/90
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 9,801,713
App. No.
14/987,601
Granted
Oct 31, 2017
Kind
B2
Abstract

The invention is directed to methods for preparing artificial heart valves by preconditioning a matrix seeded with endothelial cells and smooth muscle cells differentiated from isolated progenitor cells. These cell seeded matrices are exposed to fluid conditions that mimic blood flow through the heart to produce tissue engineered heart valves that are analogous to native heart valves.

Claims (13)

1. A preconditioned tissue engineered heart valve, comprising:

a biocompatible matrix seeded with at least one population of endothelial cells differentiated from progenitor cells ex vivo, wherein the seeded cells form at least one cell layer on the biocompatible matrix;

a population of smooth muscle cells differentiated from progenitor cells and seeded onto the endothelial cell layer,

wherein the biocompatible matrix is selected from the group consisting of a decellularized matrix, an electrospun matrix, and a synthetic polymer matrix, and

wherein at least one cell of the population of endothelial cells, the population of smooth muscle cells, or a combination thereof comprise(s) an exogenous nucleic acid encoding an anti-inflammatory factor operably linked to a promoter.

2. The heart valve of claim 1 , wherein the anti-inflammatory factor is selected from the group consisting of anti-GM-CSF, anti-TNF, anti-IL-1 and anti-IL2.

3. The heart valve of claim 1 , wherein biocompatible matrix is a decellularized heart valve.

4. The heart valve of claim 1 , wherein the electrospun matrix is a crosslinked matrix.

5. The heart valve of claim 4 , wherein the electrospun matrix comprises poly(lactide-co-glycolides) (PLGA).

6. The heart valve of claim 4 , wherein the electrospun matrix comprises nanofibers having a diameter of about 50 nanometers to about 1000 nanometers and wherein the distance between the fibers is about 50 nanometers to about 500 nanometers.

7. The heart valve of claim 4 , wherein the electrospun matrix has a pore size of about 0.1 μm 2 to about 100 μm 2 .

8. The heart valve of claim 1 , wherein the biocompatible matrix is coated with a basement membrane component.

9. The heart valve of claim 8 , wherein the basement membrane component is selected from the group consisting agar, agarose, gelatin, gum arabic, collagens, fibronectin, laminin, glycoaminoglycans, and mixtures thereof.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 4, 2016
From: ATALA, ANTHONY; YOO, JAMES J.
To: WAKE FOREST UNIVERSITY HEALTH SCIENCES
Reel/Frame 037404/0104 →
Continuity (4)
Continuation 11373066 · Mar 10, 2006
Provisional Application 60660832 · Mar 11, 2005
Provisional Application 60686316 · Jun 1, 2005
Related Publication 20160199179A1 · Jul 14, 2016