Harnessing therapeutic viruses as a delivery vehicle for RNA-based therapy.

Messenger RNA (mRNA) and microRNA (miRNA)-based therapeutics have become attractive alternatives to DNA-based therapeutics due to recent advances in manufacture, scalability and cost. Also, RNA-based therapeutics are considered safe since there are no risk of inducing genomic changes as well as the...

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Main Authors: Leena Ylösmäki, Beatrice Polini, Sara Carpi, Beatriz Martins, Elena Smertina, Sara Feola, Manlio Fusciello, Karita Peltonen, Paola Nieri, Erkko Ylösmäki, Vincenzo Cerullo
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2019-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0224072
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spelling doaj-a8eb9abbd1d84e8cbb45421a6e1213742021-03-03T21:15:43ZengPublic Library of Science (PLoS)PLoS ONE1932-62032019-01-011410e022407210.1371/journal.pone.0224072Harnessing therapeutic viruses as a delivery vehicle for RNA-based therapy.Leena YlösmäkiBeatrice PoliniSara CarpiBeatriz MartinsElena SmertinaSara FeolaManlio FuscielloKarita PeltonenPaola NieriErkko YlösmäkiVincenzo CerulloMessenger RNA (mRNA) and microRNA (miRNA)-based therapeutics have become attractive alternatives to DNA-based therapeutics due to recent advances in manufacture, scalability and cost. Also, RNA-based therapeutics are considered safe since there are no risk of inducing genomic changes as well as the potential adverse effects would be only temporary due to the transient nature of RNA-based therapeutics. However, efficient in vivo delivery of RNA-based therapeutics remains a challenge. We have developed a delivery platform for RNA-based therapeutics by exploiting the physicochemical properties of enveloped viruses. By physically attaching cationic liposome/RNA complexes onto the viral envelope of vaccinia virus, we were able to deliver mRNA, self-replicating RNA as well as miRNA inside target cells. Also, we showed that this platform, called viRNA platform, can efficiently deliver functional miRNA mimics into B16.OVA tumour in vivo.https://doi.org/10.1371/journal.pone.0224072
collection DOAJ
language English
format Article
sources DOAJ
author Leena Ylösmäki
Beatrice Polini
Sara Carpi
Beatriz Martins
Elena Smertina
Sara Feola
Manlio Fusciello
Karita Peltonen
Paola Nieri
Erkko Ylösmäki
Vincenzo Cerullo
spellingShingle Leena Ylösmäki
Beatrice Polini
Sara Carpi
Beatriz Martins
Elena Smertina
Sara Feola
Manlio Fusciello
Karita Peltonen
Paola Nieri
Erkko Ylösmäki
Vincenzo Cerullo
Harnessing therapeutic viruses as a delivery vehicle for RNA-based therapy.
PLoS ONE
author_facet Leena Ylösmäki
Beatrice Polini
Sara Carpi
Beatriz Martins
Elena Smertina
Sara Feola
Manlio Fusciello
Karita Peltonen
Paola Nieri
Erkko Ylösmäki
Vincenzo Cerullo
author_sort Leena Ylösmäki
title Harnessing therapeutic viruses as a delivery vehicle for RNA-based therapy.
title_short Harnessing therapeutic viruses as a delivery vehicle for RNA-based therapy.
title_full Harnessing therapeutic viruses as a delivery vehicle for RNA-based therapy.
title_fullStr Harnessing therapeutic viruses as a delivery vehicle for RNA-based therapy.
title_full_unstemmed Harnessing therapeutic viruses as a delivery vehicle for RNA-based therapy.
title_sort harnessing therapeutic viruses as a delivery vehicle for rna-based therapy.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2019-01-01
description Messenger RNA (mRNA) and microRNA (miRNA)-based therapeutics have become attractive alternatives to DNA-based therapeutics due to recent advances in manufacture, scalability and cost. Also, RNA-based therapeutics are considered safe since there are no risk of inducing genomic changes as well as the potential adverse effects would be only temporary due to the transient nature of RNA-based therapeutics. However, efficient in vivo delivery of RNA-based therapeutics remains a challenge. We have developed a delivery platform for RNA-based therapeutics by exploiting the physicochemical properties of enveloped viruses. By physically attaching cationic liposome/RNA complexes onto the viral envelope of vaccinia virus, we were able to deliver mRNA, self-replicating RNA as well as miRNA inside target cells. Also, we showed that this platform, called viRNA platform, can efficiently deliver functional miRNA mimics into B16.OVA tumour in vivo.
url https://doi.org/10.1371/journal.pone.0224072
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