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Adenoviral VEGF-D(ΔN ΔC) gene therapy for myocardial ischemia
Background: Cardiovascular diseases are the leading cause of death globally. In spite of the availability of improved treatments, there is still a large group of chronic ischemia patients who suffer from significant symptoms and disability. Thus, there is a clear need to develop new treatment strate...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9817830/ https://www.ncbi.nlm.nih.gov/pubmed/36619378 http://dx.doi.org/10.3389/fbioe.2022.999226 |
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author | Pajula, Juho Lähteenvuo, Johanna Lähteenvuo, Markku Honkonen, Krista Halonen, Paavo Hätinen, Olli-Pekka Kuivanen, Antti Heikkilä, Minja Nurro, Jussi Hartikainen, Juha Ylä-Herttuala, Seppo |
author_facet | Pajula, Juho Lähteenvuo, Johanna Lähteenvuo, Markku Honkonen, Krista Halonen, Paavo Hätinen, Olli-Pekka Kuivanen, Antti Heikkilä, Minja Nurro, Jussi Hartikainen, Juha Ylä-Herttuala, Seppo |
author_sort | Pajula, Juho |
collection | PubMed |
description | Background: Cardiovascular diseases are the leading cause of death globally. In spite of the availability of improved treatments, there is still a large group of chronic ischemia patients who suffer from significant symptoms and disability. Thus, there is a clear need to develop new treatment strategies for these patients. Therapeutic angiogenesis is a novel therapy method which has shown promising results in preclinical studies. In this study, we evaluated safety and efficacy of adenoviral (Ad) VEGF-D(ΔNΔC) gene transfer for the treatment of myocardial ischemia in a pig model. Methods: Adenoviral VEGF-D(ΔNΔC) gene transfer was given to pigs (n = 26) via intramyocardial injections using an electromechanical injection catheter. Angiogenic effects were evaluated in an acute myocardial infarction model (n = 18) and functionality of the lymphatic vessels were tested in healthy porcine myocardium (n = 8). AdLacZ was used as a control. Results: AdVEGF-D(ΔNΔC) induced safe and effective myocardial angiogenesis by inducing a four-fold increase in mean capillary area at the edge of the myocardial infarct six days after the gene transfer relative to the control AdLacZ group. The effect was sustained over 21 days after the gene transfer, and there were no signs of vessels regression. AdVEGF-D(ΔNΔC) also increased perfusion 3.4-fold near the infarct border zone relative to the control as measured by fluorescent microspheres. Ejection fraction was 8.7% higher in the AdVEGF-D(ΔNΔC) treated group 21 days after the gene transfer relative to the AdLacZ control group. Modified Miles assay detected a transient increase in plasma protein extravasation after the AdVEGF-D(ΔNΔC) treatment and a mild accumulation of pericardial effusate was observed at d6. However, AdVEGF-D(ΔNΔC) also induced the growth of functional lymphatic vasculature, and the amount of pericardial fluid and level of vascular permeability had returned to normal by d21. Conclusion: Endovascular intramyocardial AdVEGF-D(ΔNΔC) gene therapy proved to be safe and effective in the acute porcine myocardial infarction model and provides a new potential treatment option for patients with severe coronary heart disease. |
format | Online Article Text |
id | pubmed-9817830 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98178302023-01-07 Adenoviral VEGF-D(ΔN ΔC) gene therapy for myocardial ischemia Pajula, Juho Lähteenvuo, Johanna Lähteenvuo, Markku Honkonen, Krista Halonen, Paavo Hätinen, Olli-Pekka Kuivanen, Antti Heikkilä, Minja Nurro, Jussi Hartikainen, Juha Ylä-Herttuala, Seppo Front Bioeng Biotechnol Bioengineering and Biotechnology Background: Cardiovascular diseases are the leading cause of death globally. In spite of the availability of improved treatments, there is still a large group of chronic ischemia patients who suffer from significant symptoms and disability. Thus, there is a clear need to develop new treatment strategies for these patients. Therapeutic angiogenesis is a novel therapy method which has shown promising results in preclinical studies. In this study, we evaluated safety and efficacy of adenoviral (Ad) VEGF-D(ΔNΔC) gene transfer for the treatment of myocardial ischemia in a pig model. Methods: Adenoviral VEGF-D(ΔNΔC) gene transfer was given to pigs (n = 26) via intramyocardial injections using an electromechanical injection catheter. Angiogenic effects were evaluated in an acute myocardial infarction model (n = 18) and functionality of the lymphatic vessels were tested in healthy porcine myocardium (n = 8). AdLacZ was used as a control. Results: AdVEGF-D(ΔNΔC) induced safe and effective myocardial angiogenesis by inducing a four-fold increase in mean capillary area at the edge of the myocardial infarct six days after the gene transfer relative to the control AdLacZ group. The effect was sustained over 21 days after the gene transfer, and there were no signs of vessels regression. AdVEGF-D(ΔNΔC) also increased perfusion 3.4-fold near the infarct border zone relative to the control as measured by fluorescent microspheres. Ejection fraction was 8.7% higher in the AdVEGF-D(ΔNΔC) treated group 21 days after the gene transfer relative to the AdLacZ control group. Modified Miles assay detected a transient increase in plasma protein extravasation after the AdVEGF-D(ΔNΔC) treatment and a mild accumulation of pericardial effusate was observed at d6. However, AdVEGF-D(ΔNΔC) also induced the growth of functional lymphatic vasculature, and the amount of pericardial fluid and level of vascular permeability had returned to normal by d21. Conclusion: Endovascular intramyocardial AdVEGF-D(ΔNΔC) gene therapy proved to be safe and effective in the acute porcine myocardial infarction model and provides a new potential treatment option for patients with severe coronary heart disease. Frontiers Media S.A. 2022-12-22 /pmc/articles/PMC9817830/ /pubmed/36619378 http://dx.doi.org/10.3389/fbioe.2022.999226 Text en Copyright © 2022 Pajula, Lähteenvuo, Lähteenvuo, Honkonen, Halonen, Hätinen, Kuivanen, Heikkilä, Nurro, Hartikainen and Ylä-Herttuala. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Bioengineering and Biotechnology Pajula, Juho Lähteenvuo, Johanna Lähteenvuo, Markku Honkonen, Krista Halonen, Paavo Hätinen, Olli-Pekka Kuivanen, Antti Heikkilä, Minja Nurro, Jussi Hartikainen, Juha Ylä-Herttuala, Seppo Adenoviral VEGF-D(ΔN ΔC) gene therapy for myocardial ischemia |
title | Adenoviral VEGF-D(ΔN ΔC) gene therapy for myocardial ischemia |
title_full | Adenoviral VEGF-D(ΔN ΔC) gene therapy for myocardial ischemia |
title_fullStr | Adenoviral VEGF-D(ΔN ΔC) gene therapy for myocardial ischemia |
title_full_unstemmed | Adenoviral VEGF-D(ΔN ΔC) gene therapy for myocardial ischemia |
title_short | Adenoviral VEGF-D(ΔN ΔC) gene therapy for myocardial ischemia |
title_sort | adenoviral vegf-d(δn δc) gene therapy for myocardial ischemia |
topic | Bioengineering and Biotechnology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9817830/ https://www.ncbi.nlm.nih.gov/pubmed/36619378 http://dx.doi.org/10.3389/fbioe.2022.999226 |
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