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Updated: Nov 2, 2025

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Transplantation of a 3D Bioprinted Patch in a Murine Model of Myocardial Infarction
Published on: September 26, 2020
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Can a Biohybrid Patch Salvage Ventricular Function at a Late Time Point in the Post-Infarction Remodeling Process?
Lindemberg M Silveira-Filho1,2, Garrett N Coyan1,3, Arianna Adamo1
1McGowan Institute for Regenerative Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
JACC. Basic to Translational Science
|June 7, 2021
Summary
A novel biohybrid patch improved heart function and reduced infarct size in animal models of dilated cardiomyopathy. This cell-free patch shows promise for clinical translation in patients with heart failure.
Area of Science:
- Biomaterials science
- Cardiovascular research
- Regenerative medicine
Background:
- Large myocardial infarctions lead to heart dilation and impaired function.
- Current treatments for advanced heart failure have limitations.
- Cell-free therapeutic strategies are emerging for cardiac repair.
Purpose of the Study:
- To evaluate the efficacy of a cell-free biohybrid patch in treating large infarcted areas in dilated hearts.
- To assess the impact of the patch on cardiac morphology and function.
- To determine if the patch benefits particularly frail patients with low ejection fraction.
Main Methods:
- A biohybrid patch was implanted over infarcted regions in an animal model.
- Control groups received no patch or losartan therapy.
- Echocardiography was used to assess cardiac function and morphology.
Main Results:
- Patch implantation led to improved echocardiographic endpoints compared to control groups.
- Benefits were more pronounced in animals with pre-treatment ejection fraction below 35%.
- Patched hearts exhibited smaller infarct sizes than nonpatched hearts.
Conclusions:
- A cell-free biohybrid patch can improve ventricular remodeling and function after myocardial infarction.
- This approach may offer a promising, minimally invasive therapeutic option for heart failure patients, especially the frail.
- Further clinical translation of this biohybrid patch technology is warranted.
Keywords:
AT1R, angiotensin 1 receptorECM, extracellular matrixEDA, end-diastolic areaEF, ejection fractionESA, end-systolic areaFS, fractional shorteningHF, heart failureLV, left ventricleLVEF, left ventricular ejection fractionLVFW, left ventricular free wallLVdd, left ventricular end-diastolic diameterLVsd, left ventricular end-systolic diameterM1, macrophage type 1M2, macrophage type 2MI, myocardial infarctionMT, Masson trichromePBS, phosphate-buffered salinePECUU, poly(ester carbonate urethane) ureaPEUU, poly(ester urethane) ureaSMA, smooth muscle actinbiomaterialcardiac patchleft ventricular remodelingmyocardial infarction
