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Plant Virus-Like Particle In Situ Vaccine for Intracranial Glioma Immunotherapy

Despite aggressive multi-modality treatment with surgery, radiation and chemotherapies, malignant glioma inevitably recurs and has dismal survival rates. Recent progress in immunotherapy has led to a resurgence of interest, and immunotherapies are being investigated for treatment of glioma. However,...

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Autores principales: Kerstetter-Fogle, Amber, Shukla, Sourabh, Wang, Chao, Beiss, Veronique, Harris, Peggy L. R., Sloan, Andrew E., Steinmetz, Nicole F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6521079/
https://www.ncbi.nlm.nih.gov/pubmed/30974896
http://dx.doi.org/10.3390/cancers11040515
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author Kerstetter-Fogle, Amber
Shukla, Sourabh
Wang, Chao
Beiss, Veronique
Harris, Peggy L. R.
Sloan, Andrew E.
Steinmetz, Nicole F.
author_facet Kerstetter-Fogle, Amber
Shukla, Sourabh
Wang, Chao
Beiss, Veronique
Harris, Peggy L. R.
Sloan, Andrew E.
Steinmetz, Nicole F.
author_sort Kerstetter-Fogle, Amber
collection PubMed
description Despite aggressive multi-modality treatment with surgery, radiation and chemotherapies, malignant glioma inevitably recurs and has dismal survival rates. Recent progress in immunotherapy has led to a resurgence of interest, and immunotherapies are being investigated for treatment of glioma. However, the unique brain anatomy and a highly immunosuppressive glioma microenvironment pose significant challenges to achieving efficacy. Thus, there is a critical need for assessment of next-generation immunotherapies for glioma. In this study, we have investigated the efficacy of the nanoparticle platform technology based on plant-derived Cowpea mosaic virus like particles (empty CPMV or eCPMV) to instigate a potent immune response against intracranial glioma. CPMV immunotherapy has been shown to efficiently reverse the immunosuppressive tumor microenvironments in pre-clinical murine models of dermal melanoma and metastatic melanoma, metastatic breast cancer, intraperitoneal ovarian cancer and in canine patients with oral melanoma. In the present study, we demonstrate that in situ administration of CPMV immunotherapy in the setting of glioma can effectively recruit unique subset of effector innate and adaptive immune cells to the brain parenchyma while reducing immune suppressive cellular population, leading to regression of intracranial glioma. The in situ CPMV nanoparticle vaccine offers a potent yet safe and localized immunotherapy for intracranial glioma.
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spelling pubmed-65210792019-05-31 Plant Virus-Like Particle In Situ Vaccine for Intracranial Glioma Immunotherapy Kerstetter-Fogle, Amber Shukla, Sourabh Wang, Chao Beiss, Veronique Harris, Peggy L. R. Sloan, Andrew E. Steinmetz, Nicole F. Cancers (Basel) Article Despite aggressive multi-modality treatment with surgery, radiation and chemotherapies, malignant glioma inevitably recurs and has dismal survival rates. Recent progress in immunotherapy has led to a resurgence of interest, and immunotherapies are being investigated for treatment of glioma. However, the unique brain anatomy and a highly immunosuppressive glioma microenvironment pose significant challenges to achieving efficacy. Thus, there is a critical need for assessment of next-generation immunotherapies for glioma. In this study, we have investigated the efficacy of the nanoparticle platform technology based on plant-derived Cowpea mosaic virus like particles (empty CPMV or eCPMV) to instigate a potent immune response against intracranial glioma. CPMV immunotherapy has been shown to efficiently reverse the immunosuppressive tumor microenvironments in pre-clinical murine models of dermal melanoma and metastatic melanoma, metastatic breast cancer, intraperitoneal ovarian cancer and in canine patients with oral melanoma. In the present study, we demonstrate that in situ administration of CPMV immunotherapy in the setting of glioma can effectively recruit unique subset of effector innate and adaptive immune cells to the brain parenchyma while reducing immune suppressive cellular population, leading to regression of intracranial glioma. The in situ CPMV nanoparticle vaccine offers a potent yet safe and localized immunotherapy for intracranial glioma. MDPI 2019-04-10 /pmc/articles/PMC6521079/ /pubmed/30974896 http://dx.doi.org/10.3390/cancers11040515 Text en © 2019 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kerstetter-Fogle, Amber
Shukla, Sourabh
Wang, Chao
Beiss, Veronique
Harris, Peggy L. R.
Sloan, Andrew E.
Steinmetz, Nicole F.
Plant Virus-Like Particle In Situ Vaccine for Intracranial Glioma Immunotherapy
title Plant Virus-Like Particle In Situ Vaccine for Intracranial Glioma Immunotherapy
title_full Plant Virus-Like Particle In Situ Vaccine for Intracranial Glioma Immunotherapy
title_fullStr Plant Virus-Like Particle In Situ Vaccine for Intracranial Glioma Immunotherapy
title_full_unstemmed Plant Virus-Like Particle In Situ Vaccine for Intracranial Glioma Immunotherapy
title_short Plant Virus-Like Particle In Situ Vaccine for Intracranial Glioma Immunotherapy
title_sort plant virus-like particle in situ vaccine for intracranial glioma immunotherapy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6521079/
https://www.ncbi.nlm.nih.gov/pubmed/30974896
http://dx.doi.org/10.3390/cancers11040515
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