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Early In Vivo Experience With Tissue-Engineered Trileaflet Heart Valves

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Background —Tissue engineering is a new approach in which techniques are being developed to transplant autologous cells onto biodegradable scaffolds to ultimately form new functional autologous tissue. Workers at our laboratory have focused on tissue engineering of heart valves. The present study was designed to evaluate the implantation of a whole trileaflet tissue-engineered heart valve in the pulmonary position in a lamb model. Methods and Results —We constructed a biodegradable and biocompatible trileaflet heart valve scaffold that was fabricated from a porous polyhydroxyalkanoate (pore size 180 to 240 μm; Tepha Inc). Vascular cells were harvested from ovine carotid arteries, expanded in vitro, and seeded onto our heart valve scaffold. With the use of cardiopulmonary bypass, the native pulmonary leaflets were resected, and 2-cm segments of pulmonary artery were replaced by autologous cell–seeded heart valve constructs (n=4). One animal received an acellular valved conduit. No animal received any anticoagulation therapy. Animals were killed at 1, 5, 13, and 17 weeks. Explanted valves were examined histologically with scanning electron microscopy, biochemically, and biomechanically. All animals survived the procedure. The valves showed minimal regurgitation, and valve gradients were <20 mm Hg on echocardiography. The maximum gradient was 10 mm Hg with direct pressures. Macroscopically, the tissue-engineered constructs were covered with tissue, and there was no thrombus formation on any of the specimens. Scanning electron microscopy showed smooth flow surfaces during the follow-up period. Histological examination demonstrated laminated fibrous tissue with predominant glycosaminoglycans as extracellular matrix. 4-Hydroxyproline assays demonstrated an increase in collagen content as a percentage of native pulmonary artery (1 week 45.8%, 17 weeks 116%). DNA assays showed a comparable number of cells in all explanted samples. There was no tissue formation in the acellular control. Conclusions —Tissue-engineered heart valve scaffolds fabricated from polyhydroxyalkanoates can be used for implantation in the pulmonary position with an appropriate function for 120 days in lambs.
Title: Early In Vivo Experience With Tissue-Engineered Trileaflet Heart Valves
Description:
Background —Tissue engineering is a new approach in which techniques are being developed to transplant autologous cells onto biodegradable scaffolds to ultimately form new functional autologous tissue.
Workers at our laboratory have focused on tissue engineering of heart valves.
The present study was designed to evaluate the implantation of a whole trileaflet tissue-engineered heart valve in the pulmonary position in a lamb model.
Methods and Results —We constructed a biodegradable and biocompatible trileaflet heart valve scaffold that was fabricated from a porous polyhydroxyalkanoate (pore size 180 to 240 μm; Tepha Inc).
Vascular cells were harvested from ovine carotid arteries, expanded in vitro, and seeded onto our heart valve scaffold.
With the use of cardiopulmonary bypass, the native pulmonary leaflets were resected, and 2-cm segments of pulmonary artery were replaced by autologous cell–seeded heart valve constructs (n=4).
One animal received an acellular valved conduit.
No animal received any anticoagulation therapy.
Animals were killed at 1, 5, 13, and 17 weeks.
Explanted valves were examined histologically with scanning electron microscopy, biochemically, and biomechanically.
All animals survived the procedure.
The valves showed minimal regurgitation, and valve gradients were <20 mm Hg on echocardiography.
The maximum gradient was 10 mm Hg with direct pressures.
Macroscopically, the tissue-engineered constructs were covered with tissue, and there was no thrombus formation on any of the specimens.
Scanning electron microscopy showed smooth flow surfaces during the follow-up period.
Histological examination demonstrated laminated fibrous tissue with predominant glycosaminoglycans as extracellular matrix.
4-Hydroxyproline assays demonstrated an increase in collagen content as a percentage of native pulmonary artery (1 week 45.
8%, 17 weeks 116%).
DNA assays showed a comparable number of cells in all explanted samples.
There was no tissue formation in the acellular control.
Conclusions —Tissue-engineered heart valve scaffolds fabricated from polyhydroxyalkanoates can be used for implantation in the pulmonary position with an appropriate function for 120 days in lambs.

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