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Artificially cloaked viral nanovaccine for cancer immunotherapy

Virus-based cancer vaccines are nowadays considered an interesting approach in the field of cancer immunotherapy, despite the observation that the majority of the immune responses they elicit are against the virus and not against the tumor. In contrast, targeting tumor associated antigens is effecti...

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Autores principales: Fusciello, Manlio, Fontana, Flavia, Tähtinen, Siri, Capasso, Cristian, Feola, Sara, Martins, Beatriz, Chiaro, Jacopo, Peltonen, Karita, Ylösmäki, Leena, Ylösmäki, Erkko, Hamdan, Firas, Kari, Otto K., Ndika, Joseph, Alenius, Harri, Urtti, Arto, Hirvonen, Jouni T., Santos, Hélder A., Cerullo, Vincenzo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6917704/
https://www.ncbi.nlm.nih.gov/pubmed/31848338
http://dx.doi.org/10.1038/s41467-019-13744-8
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author Fusciello, Manlio
Fontana, Flavia
Tähtinen, Siri
Capasso, Cristian
Feola, Sara
Martins, Beatriz
Chiaro, Jacopo
Peltonen, Karita
Ylösmäki, Leena
Ylösmäki, Erkko
Hamdan, Firas
Kari, Otto K.
Ndika, Joseph
Alenius, Harri
Urtti, Arto
Hirvonen, Jouni T.
Santos, Hélder A.
Cerullo, Vincenzo
author_facet Fusciello, Manlio
Fontana, Flavia
Tähtinen, Siri
Capasso, Cristian
Feola, Sara
Martins, Beatriz
Chiaro, Jacopo
Peltonen, Karita
Ylösmäki, Leena
Ylösmäki, Erkko
Hamdan, Firas
Kari, Otto K.
Ndika, Joseph
Alenius, Harri
Urtti, Arto
Hirvonen, Jouni T.
Santos, Hélder A.
Cerullo, Vincenzo
author_sort Fusciello, Manlio
collection PubMed
description Virus-based cancer vaccines are nowadays considered an interesting approach in the field of cancer immunotherapy, despite the observation that the majority of the immune responses they elicit are against the virus and not against the tumor. In contrast, targeting tumor associated antigens is effective, however the identification of these antigens remains challenging. Here, we describe ExtraCRAd, a multi-vaccination strategy focused on an oncolytic virus artificially wrapped with tumor cancer membranes carrying tumor antigens. We demonstrate that ExtraCRAd displays increased infectivity and oncolytic effect in vitro and in vivo. We show that this nanoparticle platform controls the growth of aggressive melanoma and lung tumors in vivo both in preventive and therapeutic setting, creating a highly specific anti-cancer immune response. In conclusion, ExtraCRAd might serve as the next generation of personalized cancer vaccines with enhanced features over standard vaccination regimens, representing an alternative way to target cancer.
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spelling pubmed-69177042019-12-19 Artificially cloaked viral nanovaccine for cancer immunotherapy Fusciello, Manlio Fontana, Flavia Tähtinen, Siri Capasso, Cristian Feola, Sara Martins, Beatriz Chiaro, Jacopo Peltonen, Karita Ylösmäki, Leena Ylösmäki, Erkko Hamdan, Firas Kari, Otto K. Ndika, Joseph Alenius, Harri Urtti, Arto Hirvonen, Jouni T. Santos, Hélder A. Cerullo, Vincenzo Nat Commun Article Virus-based cancer vaccines are nowadays considered an interesting approach in the field of cancer immunotherapy, despite the observation that the majority of the immune responses they elicit are against the virus and not against the tumor. In contrast, targeting tumor associated antigens is effective, however the identification of these antigens remains challenging. Here, we describe ExtraCRAd, a multi-vaccination strategy focused on an oncolytic virus artificially wrapped with tumor cancer membranes carrying tumor antigens. We demonstrate that ExtraCRAd displays increased infectivity and oncolytic effect in vitro and in vivo. We show that this nanoparticle platform controls the growth of aggressive melanoma and lung tumors in vivo both in preventive and therapeutic setting, creating a highly specific anti-cancer immune response. In conclusion, ExtraCRAd might serve as the next generation of personalized cancer vaccines with enhanced features over standard vaccination regimens, representing an alternative way to target cancer. Nature Publishing Group UK 2019-12-17 /pmc/articles/PMC6917704/ /pubmed/31848338 http://dx.doi.org/10.1038/s41467-019-13744-8 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Fusciello, Manlio
Fontana, Flavia
Tähtinen, Siri
Capasso, Cristian
Feola, Sara
Martins, Beatriz
Chiaro, Jacopo
Peltonen, Karita
Ylösmäki, Leena
Ylösmäki, Erkko
Hamdan, Firas
Kari, Otto K.
Ndika, Joseph
Alenius, Harri
Urtti, Arto
Hirvonen, Jouni T.
Santos, Hélder A.
Cerullo, Vincenzo
Artificially cloaked viral nanovaccine for cancer immunotherapy
title Artificially cloaked viral nanovaccine for cancer immunotherapy
title_full Artificially cloaked viral nanovaccine for cancer immunotherapy
title_fullStr Artificially cloaked viral nanovaccine for cancer immunotherapy
title_full_unstemmed Artificially cloaked viral nanovaccine for cancer immunotherapy
title_short Artificially cloaked viral nanovaccine for cancer immunotherapy
title_sort artificially cloaked viral nanovaccine for cancer immunotherapy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6917704/
https://www.ncbi.nlm.nih.gov/pubmed/31848338
http://dx.doi.org/10.1038/s41467-019-13744-8
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