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Irradiation or temozolomide chemotherapy enhances anti-CD47 treatment of glioblastoma
Irradiation and temozolomide (TMZ) chemotherapy are the current standard treatments for glioblastoma multiforme (GBM), but they are associated with toxicity and limited efficacy. Recently, these standard therapies have been used to enhance immunotherapy against GBM. Immunotherapy using the anti-CD47...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7016411/ https://www.ncbi.nlm.nih.gov/pubmed/31547758 http://dx.doi.org/10.1177/1753425919876690 |
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author | Gholamin, Sharareh Youssef, Osama A Rafat, Marjan Esparza, Rogelio Kahn, Suzana Shahin, Maryam Giaccia, Amato J Graves, Edward E Weissman, Irving Mitra, Siddhartha Cheshier, Samuel H |
author_facet | Gholamin, Sharareh Youssef, Osama A Rafat, Marjan Esparza, Rogelio Kahn, Suzana Shahin, Maryam Giaccia, Amato J Graves, Edward E Weissman, Irving Mitra, Siddhartha Cheshier, Samuel H |
author_sort | Gholamin, Sharareh |
collection | PubMed |
description | Irradiation and temozolomide (TMZ) chemotherapy are the current standard treatments for glioblastoma multiforme (GBM), but they are associated with toxicity and limited efficacy. Recently, these standard therapies have been used to enhance immunotherapy against GBM. Immunotherapy using the anti-CD47 (immune checkpoint inhibitor) treatment has shown promise in treating multiple tumor types, including GBM. The goal of this current work was to test whether irradiation or TMZ chemotherapy could enhance anti-CD47 treatment against GBM. Our results showed that irradiation and TMZ each significantly enhanced anti-CD47-mediated phagocytosis of GBM cells in vitro. Furthermore, mice engrafted with human GBM that received anti-CD47 combined with focal irradiation or TMZ treatment showed a significant increase in the survival rate compared to those that received a single treatment. The tumor growth in mice that received both anti-CD47 and irradiation was significantly less than that of groups that received either anti-CD47 or focal irradiation. The results from this study may support future use of anti-CD47 treatment in combination with irradiation or chemotherapy to enhance the therapeutic efficacy of GBM treatment. |
format | Online Article Text |
id | pubmed-7016411 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-70164112020-02-27 Irradiation or temozolomide chemotherapy enhances anti-CD47 treatment of glioblastoma Gholamin, Sharareh Youssef, Osama A Rafat, Marjan Esparza, Rogelio Kahn, Suzana Shahin, Maryam Giaccia, Amato J Graves, Edward E Weissman, Irving Mitra, Siddhartha Cheshier, Samuel H Innate Immun Original Articles Irradiation and temozolomide (TMZ) chemotherapy are the current standard treatments for glioblastoma multiforme (GBM), but they are associated with toxicity and limited efficacy. Recently, these standard therapies have been used to enhance immunotherapy against GBM. Immunotherapy using the anti-CD47 (immune checkpoint inhibitor) treatment has shown promise in treating multiple tumor types, including GBM. The goal of this current work was to test whether irradiation or TMZ chemotherapy could enhance anti-CD47 treatment against GBM. Our results showed that irradiation and TMZ each significantly enhanced anti-CD47-mediated phagocytosis of GBM cells in vitro. Furthermore, mice engrafted with human GBM that received anti-CD47 combined with focal irradiation or TMZ treatment showed a significant increase in the survival rate compared to those that received a single treatment. The tumor growth in mice that received both anti-CD47 and irradiation was significantly less than that of groups that received either anti-CD47 or focal irradiation. The results from this study may support future use of anti-CD47 treatment in combination with irradiation or chemotherapy to enhance the therapeutic efficacy of GBM treatment. SAGE Publications 2019-09-23 2020-02 /pmc/articles/PMC7016411/ /pubmed/31547758 http://dx.doi.org/10.1177/1753425919876690 Text en © The Author(s) 2019 http://creativecommons.org/licenses/by/4.0/ Creative Commons CC BY: This article is distributed under the terms of the Creative Commons Attribution 4.0 License (http://www.creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Articles Gholamin, Sharareh Youssef, Osama A Rafat, Marjan Esparza, Rogelio Kahn, Suzana Shahin, Maryam Giaccia, Amato J Graves, Edward E Weissman, Irving Mitra, Siddhartha Cheshier, Samuel H Irradiation or temozolomide chemotherapy enhances anti-CD47 treatment of glioblastoma |
title | Irradiation or temozolomide chemotherapy enhances anti-CD47 treatment of glioblastoma |
title_full | Irradiation or temozolomide chemotherapy enhances anti-CD47 treatment of glioblastoma |
title_fullStr | Irradiation or temozolomide chemotherapy enhances anti-CD47 treatment of glioblastoma |
title_full_unstemmed | Irradiation or temozolomide chemotherapy enhances anti-CD47 treatment of glioblastoma |
title_short | Irradiation or temozolomide chemotherapy enhances anti-CD47 treatment of glioblastoma |
title_sort | irradiation or temozolomide chemotherapy enhances anti-cd47 treatment of glioblastoma |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7016411/ https://www.ncbi.nlm.nih.gov/pubmed/31547758 http://dx.doi.org/10.1177/1753425919876690 |
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