miR-199a carried by adeno-associated virus serotype 6 (AAV6) proved cardioreparative in a pig model when administered early after myocardial infarction (MI). To test whether the therapeutic efficacy of miR-199a is maintained when its administration is delayed, AAV6-miR-199a or a control AAV6 were injected 1 or 2 weeks after MI. Scar mass and cardiac contractile performance parameters were not significantly different between AAV6-miR-199a–treated and AAV6-control pigs. Nonetheless, most AAV6-miR-199a–treated pigs died from sudden death at 40 to 52 days after vector administration. For clinical translation, it appears mandatory to administer miR-199a early after MI and through modalities other than permanent expression from a viral vector.

Delayed miR-199a Administration After Myocardial Infarction Precludes Pro-Regenerative Effects

Burjanadze, Gia;Gorgodze, Nikoloz;Gabisonia, Khatia;Carlucci, Lucia;Bernini, Fabio;Giacca, Mauro;Recchia, Fabio A.
2025-01-01

Abstract

miR-199a carried by adeno-associated virus serotype 6 (AAV6) proved cardioreparative in a pig model when administered early after myocardial infarction (MI). To test whether the therapeutic efficacy of miR-199a is maintained when its administration is delayed, AAV6-miR-199a or a control AAV6 were injected 1 or 2 weeks after MI. Scar mass and cardiac contractile performance parameters were not significantly different between AAV6-miR-199a–treated and AAV6-control pigs. Nonetheless, most AAV6-miR-199a–treated pigs died from sudden death at 40 to 52 days after vector administration. For clinical translation, it appears mandatory to administer miR-199a early after MI and through modalities other than permanent expression from a viral vector.
2025
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11382/588105
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