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GD2 CAR T cells against human glioblastoma
Glioblastoma is the most malignant primary brain tumor and is still in need of effective medical treatment. We isolated patient-derived glioblastoma cells showing high GD2 antigen expression representing a potential target for CAR T strategy. Data highlighted a robust GD2 CAR antitumor potential in...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8551169/ https://www.ncbi.nlm.nih.gov/pubmed/34707200 http://dx.doi.org/10.1038/s41698-021-00233-9 |
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author | Prapa, Malvina Chiavelli, Chiara Golinelli, Giulia Grisendi, Giulia Bestagno, Marco Di Tinco, Rosanna Dall’Ora, Massimiliano Neri, Giovanni Candini, Olivia Spano, Carlotta Petrachi, Tiziana Bertoni, Laura Carnevale, Gianluca Pugliese, Giuseppe Depenni, Roberta Feletti, Alberto Iaccarino, Corrado Pavesi, Giacomo Dominici, Massimo |
author_facet | Prapa, Malvina Chiavelli, Chiara Golinelli, Giulia Grisendi, Giulia Bestagno, Marco Di Tinco, Rosanna Dall’Ora, Massimiliano Neri, Giovanni Candini, Olivia Spano, Carlotta Petrachi, Tiziana Bertoni, Laura Carnevale, Gianluca Pugliese, Giuseppe Depenni, Roberta Feletti, Alberto Iaccarino, Corrado Pavesi, Giacomo Dominici, Massimo |
author_sort | Prapa, Malvina |
collection | PubMed |
description | Glioblastoma is the most malignant primary brain tumor and is still in need of effective medical treatment. We isolated patient-derived glioblastoma cells showing high GD2 antigen expression representing a potential target for CAR T strategy. Data highlighted a robust GD2 CAR antitumor potential in 2D and 3D glioblastoma models associated with a significant and CAR T-restricted increase of selected cytokines. Interestingly, immunosuppressant TGF β1, expressed in all co-cultures, did not influence antitumor activity. The orthotopic NOD/SCID models using primary glioblastoma cells reproduced human histopathological features. Considering still-conflicting data on the delivery route for targeting brain tumors, we compared intracerebral versus intravenous CAR T injections. We report that the intracerebral route significantly increased the length of survival time in a dose-dependent manner, without any side effects. Collectively, the proposed anti-GD2 CAR can counteract human glioblastoma potentially opening a new therapeutic option for a still incurable cancer. |
format | Online Article Text |
id | pubmed-8551169 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-85511692021-10-29 GD2 CAR T cells against human glioblastoma Prapa, Malvina Chiavelli, Chiara Golinelli, Giulia Grisendi, Giulia Bestagno, Marco Di Tinco, Rosanna Dall’Ora, Massimiliano Neri, Giovanni Candini, Olivia Spano, Carlotta Petrachi, Tiziana Bertoni, Laura Carnevale, Gianluca Pugliese, Giuseppe Depenni, Roberta Feletti, Alberto Iaccarino, Corrado Pavesi, Giacomo Dominici, Massimo NPJ Precis Oncol Article Glioblastoma is the most malignant primary brain tumor and is still in need of effective medical treatment. We isolated patient-derived glioblastoma cells showing high GD2 antigen expression representing a potential target for CAR T strategy. Data highlighted a robust GD2 CAR antitumor potential in 2D and 3D glioblastoma models associated with a significant and CAR T-restricted increase of selected cytokines. Interestingly, immunosuppressant TGF β1, expressed in all co-cultures, did not influence antitumor activity. The orthotopic NOD/SCID models using primary glioblastoma cells reproduced human histopathological features. Considering still-conflicting data on the delivery route for targeting brain tumors, we compared intracerebral versus intravenous CAR T injections. We report that the intracerebral route significantly increased the length of survival time in a dose-dependent manner, without any side effects. Collectively, the proposed anti-GD2 CAR can counteract human glioblastoma potentially opening a new therapeutic option for a still incurable cancer. Nature Publishing Group UK 2021-10-27 /pmc/articles/PMC8551169/ /pubmed/34707200 http://dx.doi.org/10.1038/s41698-021-00233-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Prapa, Malvina Chiavelli, Chiara Golinelli, Giulia Grisendi, Giulia Bestagno, Marco Di Tinco, Rosanna Dall’Ora, Massimiliano Neri, Giovanni Candini, Olivia Spano, Carlotta Petrachi, Tiziana Bertoni, Laura Carnevale, Gianluca Pugliese, Giuseppe Depenni, Roberta Feletti, Alberto Iaccarino, Corrado Pavesi, Giacomo Dominici, Massimo GD2 CAR T cells against human glioblastoma |
title | GD2 CAR T cells against human glioblastoma |
title_full | GD2 CAR T cells against human glioblastoma |
title_fullStr | GD2 CAR T cells against human glioblastoma |
title_full_unstemmed | GD2 CAR T cells against human glioblastoma |
title_short | GD2 CAR T cells against human glioblastoma |
title_sort | gd2 car t cells against human glioblastoma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8551169/ https://www.ncbi.nlm.nih.gov/pubmed/34707200 http://dx.doi.org/10.1038/s41698-021-00233-9 |
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