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Potent and Targeted Sindbis Virus Platform for Immunotherapy of Ovarian Cancer

Our laboratory has been developing a Sindbis viral (SV) vector platform for treatments of ovarian and other types of cancers. In this study we show that SV.IL-12 combined with an agonistic OX40 antibody can eliminate ovarian cancer in a Mouse Ovarian Surface Epithelial Cell Line (MOSEC) model and fu...

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Autores principales: Opp, Silvana, Hurtado, Alicia, Pampeno, Christine, Lin, Ziyan, Meruelo, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9818975/
https://www.ncbi.nlm.nih.gov/pubmed/36611875
http://dx.doi.org/10.3390/cells12010077
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author Opp, Silvana
Hurtado, Alicia
Pampeno, Christine
Lin, Ziyan
Meruelo, Daniel
author_facet Opp, Silvana
Hurtado, Alicia
Pampeno, Christine
Lin, Ziyan
Meruelo, Daniel
author_sort Opp, Silvana
collection PubMed
description Our laboratory has been developing a Sindbis viral (SV) vector platform for treatments of ovarian and other types of cancers. In this study we show that SV.IL-12 combined with an agonistic OX40 antibody can eliminate ovarian cancer in a Mouse Ovarian Surface Epithelial Cell Line (MOSEC) model and further prevent tumors in mice rechallenged with tumor cells after approximately 5 months. Treatment efficacy is shown to be dependent upon T-cells that are transcriptionally and metabolically reprogramed. An influx of immune cells to the tumor microenvironment occurs. Combination of sequences encoding both IL-12 and anti-OX40 into a single SV vector, SV.IgGOX40.IL-12, facilitates the local delivery of immunoregulatory agents to tumors enhancing the anti-tumor response. We promote SV.IgGOX40.IL-12 as a safe and effective therapy for multiple types of cancer.
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spelling pubmed-98189752023-01-07 Potent and Targeted Sindbis Virus Platform for Immunotherapy of Ovarian Cancer Opp, Silvana Hurtado, Alicia Pampeno, Christine Lin, Ziyan Meruelo, Daniel Cells Article Our laboratory has been developing a Sindbis viral (SV) vector platform for treatments of ovarian and other types of cancers. In this study we show that SV.IL-12 combined with an agonistic OX40 antibody can eliminate ovarian cancer in a Mouse Ovarian Surface Epithelial Cell Line (MOSEC) model and further prevent tumors in mice rechallenged with tumor cells after approximately 5 months. Treatment efficacy is shown to be dependent upon T-cells that are transcriptionally and metabolically reprogramed. An influx of immune cells to the tumor microenvironment occurs. Combination of sequences encoding both IL-12 and anti-OX40 into a single SV vector, SV.IgGOX40.IL-12, facilitates the local delivery of immunoregulatory agents to tumors enhancing the anti-tumor response. We promote SV.IgGOX40.IL-12 as a safe and effective therapy for multiple types of cancer. MDPI 2022-12-24 /pmc/articles/PMC9818975/ /pubmed/36611875 http://dx.doi.org/10.3390/cells12010077 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Opp, Silvana
Hurtado, Alicia
Pampeno, Christine
Lin, Ziyan
Meruelo, Daniel
Potent and Targeted Sindbis Virus Platform for Immunotherapy of Ovarian Cancer
title Potent and Targeted Sindbis Virus Platform for Immunotherapy of Ovarian Cancer
title_full Potent and Targeted Sindbis Virus Platform for Immunotherapy of Ovarian Cancer
title_fullStr Potent and Targeted Sindbis Virus Platform for Immunotherapy of Ovarian Cancer
title_full_unstemmed Potent and Targeted Sindbis Virus Platform for Immunotherapy of Ovarian Cancer
title_short Potent and Targeted Sindbis Virus Platform for Immunotherapy of Ovarian Cancer
title_sort potent and targeted sindbis virus platform for immunotherapy of ovarian cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9818975/
https://www.ncbi.nlm.nih.gov/pubmed/36611875
http://dx.doi.org/10.3390/cells12010077
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