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CAR T Cell Therapy in Primary Brain Tumors: Current Investigations and the Future
Chimeric antigen receptor T cells (CAR T cells) are engineered cells expressing a chimeric antigen receptor (CAR) against a specific tumor antigen (TA) that allows for the identification and elimination of cancer cells. The remarkable clinical effect seen with CAR T cell therapies against hematologi...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8899093/ https://www.ncbi.nlm.nih.gov/pubmed/35265074 http://dx.doi.org/10.3389/fimmu.2022.817296 |
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author | Lin, Ya-Jui Mashouf, Leila A. Lim, Michael |
author_facet | Lin, Ya-Jui Mashouf, Leila A. Lim, Michael |
author_sort | Lin, Ya-Jui |
collection | PubMed |
description | Chimeric antigen receptor T cells (CAR T cells) are engineered cells expressing a chimeric antigen receptor (CAR) against a specific tumor antigen (TA) that allows for the identification and elimination of cancer cells. The remarkable clinical effect seen with CAR T cell therapies against hematological malignancies have attracted interest in developing such therapies for solid tumors, including brain tumors. Glioblastoma (GBM) is the most common primary brain tumor in adults and is associated with poor prognosis due to its highly aggressive nature. Pediatric brain cancers are similarly aggressive and thus are a major cause of pediatric cancer-related death. CAR T cell therapy represents a promising avenue for therapy against these malignancies. Several specific TAs, such as EGFR/EGFRvIII, IL13Rα2, B7-H3, and HER2, have been targeted in preclinical studies and clinical trials. Unfortunately, CAR T cells against brain tumors have showed limited efficacy due to TA heterogeneity, difficulty trafficking from blood to tumor sites, and the immunosuppressive tumor microenvironment. Here, we review current CAR T cell approaches in treating cancers, with particular focus on brain cancers. We also describe a novel technique of focused ultrasound controlling the activation of engineered CAR T cells to achieve the safer cell therapies. Finally, we summarize the development of combinational strategies to improve the efficacy and overcome historical limitations of CAR T cell therapy. |
format | Online Article Text |
id | pubmed-8899093 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-88990932022-03-08 CAR T Cell Therapy in Primary Brain Tumors: Current Investigations and the Future Lin, Ya-Jui Mashouf, Leila A. Lim, Michael Front Immunol Immunology Chimeric antigen receptor T cells (CAR T cells) are engineered cells expressing a chimeric antigen receptor (CAR) against a specific tumor antigen (TA) that allows for the identification and elimination of cancer cells. The remarkable clinical effect seen with CAR T cell therapies against hematological malignancies have attracted interest in developing such therapies for solid tumors, including brain tumors. Glioblastoma (GBM) is the most common primary brain tumor in adults and is associated with poor prognosis due to its highly aggressive nature. Pediatric brain cancers are similarly aggressive and thus are a major cause of pediatric cancer-related death. CAR T cell therapy represents a promising avenue for therapy against these malignancies. Several specific TAs, such as EGFR/EGFRvIII, IL13Rα2, B7-H3, and HER2, have been targeted in preclinical studies and clinical trials. Unfortunately, CAR T cells against brain tumors have showed limited efficacy due to TA heterogeneity, difficulty trafficking from blood to tumor sites, and the immunosuppressive tumor microenvironment. Here, we review current CAR T cell approaches in treating cancers, with particular focus on brain cancers. We also describe a novel technique of focused ultrasound controlling the activation of engineered CAR T cells to achieve the safer cell therapies. Finally, we summarize the development of combinational strategies to improve the efficacy and overcome historical limitations of CAR T cell therapy. Frontiers Media S.A. 2022-02-21 /pmc/articles/PMC8899093/ /pubmed/35265074 http://dx.doi.org/10.3389/fimmu.2022.817296 Text en Copyright © 2022 Lin, Mashouf and Lim https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Lin, Ya-Jui Mashouf, Leila A. Lim, Michael CAR T Cell Therapy in Primary Brain Tumors: Current Investigations and the Future |
title | CAR T Cell Therapy in Primary Brain Tumors: Current Investigations and the Future |
title_full | CAR T Cell Therapy in Primary Brain Tumors: Current Investigations and the Future |
title_fullStr | CAR T Cell Therapy in Primary Brain Tumors: Current Investigations and the Future |
title_full_unstemmed | CAR T Cell Therapy in Primary Brain Tumors: Current Investigations and the Future |
title_short | CAR T Cell Therapy in Primary Brain Tumors: Current Investigations and the Future |
title_sort | car t cell therapy in primary brain tumors: current investigations and the future |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8899093/ https://www.ncbi.nlm.nih.gov/pubmed/35265074 http://dx.doi.org/10.3389/fimmu.2022.817296 |
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