Efficacy and safety of myocardial gene transfer of adenovirus, adeno-associated virus and lentivirus vectors in the mouse heart
Autor: | V. Parviainen, Jenni Huusko, S. Pikkarainen, Marja Hedman, Mateusz Mendel, Mari Merentie, Nihay Laham-Karam, Seppo Ylä-Herttuala, Line Lottonen-Raikaslehto, Vesa Kärjä, Riina Rissanen |
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Rok vydání: | 2015 |
Předmět: |
0301 basic medicine
Cardiac function curve medicine.medical_specialty Heart Diseases viruses Genetic enhancement Genetic Vectors Echocardiography Three-Dimensional Diastole Gene delivery Biology medicine.disease_cause Adenoviridae Mice 03 medical and health sciences Fibrosis Internal medicine Genetics medicine Animals Molecular Biology Adeno-associated virus Lentivirus Genetic Therapy Dependovirus medicine.disease 030104 developmental biology medicine.anatomical_structure Ventricle Immunology Cardiology Systemic administration Molecular Medicine |
Zdroj: | Gene Therapy. 23:296-305 |
ISSN: | 1476-5462 0969-7128 |
DOI: | 10.1038/gt.2015.114 |
Popis: | Gene therapy is a promising new treatment option for cardiac diseases. For finding the most suitable and safe vector for cardiac gene transfer, we delivered adenovirus (AdV), adeno-associated virus (AAV) and lentivirus (LeV) vectors into the mouse heart with sophisticated closed-chest echocardiography-guided intramyocardial injection method for comparing them with regards to transduction efficiency, myocardial damage, effects on the left ventricular function and electrocardiography (ECG). AdV had the highest transduction efficiency in cardiomyocytes followed by AAV2 and AAV9, and the lowest efficiency was seen with LeV. The local myocardial inflammation and fibrosis in the left ventricle (LV) was proportional to transduction efficiency. AdV caused LV dilatation and systolic dysfunction. Neither of the locally injected AAV serotypes impaired the LV systolic function, but AAV9 caused diastolic dysfunction to some extent. LeV did not affect the cardiac function. We also studied systemic delivery of AAV9, which led to transduction of cardiomyocytes throughout the myocardium. However, also diffuse fibrosis was present leading to significantly impaired LV systolic and diastolic function and pathological ECG changes. Compared with widely used AdV vector, AAV2, AAV9 and LeV were less effective in transducing cardiomyocytes but also less harmful. Local administration of AAV9 was safer and more efficient compared with systemic administration. |
Databáze: | OpenAIRE |
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