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Repurposing the yellow fever vaccine for intratumoral immunotherapy

Live 17D is widely used as a prophylactic vaccine strain for yellow fever virus that induces potent neutralizing humoral and cellular immunity against the wild‐type pathogen. 17D replicates and kills mouse and human tumor cell lines but not non‐transformed human cells. Intratumoral injections with v...

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Autores principales: Aznar, Maria Angela, Molina, Carmen, Teijeira, Alvaro, Rodriguez, Inmaculada, Azpilikueta, Arantza, Garasa, Saray, Sanchez‐Paulete, Alfonso R, Cordeiro, Luna, Etxeberria, Iñaki, Alvarez, Maite, Rius‐Rocabert, Sergio, Nistal‐Villan, Estanislao, Berraondo, Pedro, Melero, Ignacio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6949490/
https://www.ncbi.nlm.nih.gov/pubmed/31746149
http://dx.doi.org/10.15252/emmm.201910375
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author Aznar, Maria Angela
Molina, Carmen
Teijeira, Alvaro
Rodriguez, Inmaculada
Azpilikueta, Arantza
Garasa, Saray
Sanchez‐Paulete, Alfonso R
Cordeiro, Luna
Etxeberria, Iñaki
Alvarez, Maite
Rius‐Rocabert, Sergio
Nistal‐Villan, Estanislao
Berraondo, Pedro
Melero, Ignacio
author_facet Aznar, Maria Angela
Molina, Carmen
Teijeira, Alvaro
Rodriguez, Inmaculada
Azpilikueta, Arantza
Garasa, Saray
Sanchez‐Paulete, Alfonso R
Cordeiro, Luna
Etxeberria, Iñaki
Alvarez, Maite
Rius‐Rocabert, Sergio
Nistal‐Villan, Estanislao
Berraondo, Pedro
Melero, Ignacio
author_sort Aznar, Maria Angela
collection PubMed
description Live 17D is widely used as a prophylactic vaccine strain for yellow fever virus that induces potent neutralizing humoral and cellular immunity against the wild‐type pathogen. 17D replicates and kills mouse and human tumor cell lines but not non‐transformed human cells. Intratumoral injections with viable 17D markedly delay transplanted tumor progression in a CD8 T‐cell‐dependent manner. In mice bearing bilateral tumors in which only one is intratumorally injected, contralateral therapeutic effects are observed consistent with more prominent CD8 T‐cell infiltrates and a treatment‐related reduction of Tregs. Additive efficacy effects were observed upon co‐treatment with intratumoral 17D and systemic anti‐CD137 and anti‐PD‐1 immunostimulatory monoclonal antibodies. Importantly, when mice were preimmunized with 17D, intratumoral 17D treatment achieved better local and distant antitumor immunity. Such beneficial effects of prevaccination are in part explained by the potentiation of CD4 and CD8 T‐cell infiltration in the treated tumor. The repurposed use of a GMP‐grade vaccine to be given via the intratumoral route in prevaccinated patients constitutes a clinically feasible and safe immunotherapy approach.
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spelling pubmed-69494902020-01-10 Repurposing the yellow fever vaccine for intratumoral immunotherapy Aznar, Maria Angela Molina, Carmen Teijeira, Alvaro Rodriguez, Inmaculada Azpilikueta, Arantza Garasa, Saray Sanchez‐Paulete, Alfonso R Cordeiro, Luna Etxeberria, Iñaki Alvarez, Maite Rius‐Rocabert, Sergio Nistal‐Villan, Estanislao Berraondo, Pedro Melero, Ignacio EMBO Mol Med Articles Live 17D is widely used as a prophylactic vaccine strain for yellow fever virus that induces potent neutralizing humoral and cellular immunity against the wild‐type pathogen. 17D replicates and kills mouse and human tumor cell lines but not non‐transformed human cells. Intratumoral injections with viable 17D markedly delay transplanted tumor progression in a CD8 T‐cell‐dependent manner. In mice bearing bilateral tumors in which only one is intratumorally injected, contralateral therapeutic effects are observed consistent with more prominent CD8 T‐cell infiltrates and a treatment‐related reduction of Tregs. Additive efficacy effects were observed upon co‐treatment with intratumoral 17D and systemic anti‐CD137 and anti‐PD‐1 immunostimulatory monoclonal antibodies. Importantly, when mice were preimmunized with 17D, intratumoral 17D treatment achieved better local and distant antitumor immunity. Such beneficial effects of prevaccination are in part explained by the potentiation of CD4 and CD8 T‐cell infiltration in the treated tumor. The repurposed use of a GMP‐grade vaccine to be given via the intratumoral route in prevaccinated patients constitutes a clinically feasible and safe immunotherapy approach. John Wiley and Sons Inc. 2019-11-19 2020-01-09 /pmc/articles/PMC6949490/ /pubmed/31746149 http://dx.doi.org/10.15252/emmm.201910375 Text en © 2019 The Authors. Published under the terms of the CC BY 4.0 license This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Aznar, Maria Angela
Molina, Carmen
Teijeira, Alvaro
Rodriguez, Inmaculada
Azpilikueta, Arantza
Garasa, Saray
Sanchez‐Paulete, Alfonso R
Cordeiro, Luna
Etxeberria, Iñaki
Alvarez, Maite
Rius‐Rocabert, Sergio
Nistal‐Villan, Estanislao
Berraondo, Pedro
Melero, Ignacio
Repurposing the yellow fever vaccine for intratumoral immunotherapy
title Repurposing the yellow fever vaccine for intratumoral immunotherapy
title_full Repurposing the yellow fever vaccine for intratumoral immunotherapy
title_fullStr Repurposing the yellow fever vaccine for intratumoral immunotherapy
title_full_unstemmed Repurposing the yellow fever vaccine for intratumoral immunotherapy
title_short Repurposing the yellow fever vaccine for intratumoral immunotherapy
title_sort repurposing the yellow fever vaccine for intratumoral immunotherapy
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6949490/
https://www.ncbi.nlm.nih.gov/pubmed/31746149
http://dx.doi.org/10.15252/emmm.201910375
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