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Immunotherapy for Pediatric Brain Tumors
Malignant brain tumors are the most common cause of solid cancer death in children. New targeted therapies are vital to improve treatment outcomes, but must be developed to enable trafficking across the blood brain barrier (BBB). Since activated T cells cross the BBB, cancer immunotherapy can be har...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5664064/ https://www.ncbi.nlm.nih.gov/pubmed/29065490 http://dx.doi.org/10.3390/brainsci7100137 |
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author | Sayour, Elias J. Mitchell, Duane A. |
author_facet | Sayour, Elias J. Mitchell, Duane A. |
author_sort | Sayour, Elias J. |
collection | PubMed |
description | Malignant brain tumors are the most common cause of solid cancer death in children. New targeted therapies are vital to improve treatment outcomes, but must be developed to enable trafficking across the blood brain barrier (BBB). Since activated T cells cross the BBB, cancer immunotherapy can be harnessed to unlock the cytotoxic potential of the immune system. However, standard of care treatments (i.e., chemotherapy and radiation) applied concomitant to pediatric brain tumor immunotherapy may abrogate induction of immunotherapeutic responses. This review will discuss the development of immunotherapies within this paradigm using emerging approaches being investigated in phase I/II trials in children with refractory brain tumors, including checkpoint inhibitors, vaccine immunotherapy, and adoptive cell therapy. |
format | Online Article Text |
id | pubmed-5664064 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-56640642017-11-06 Immunotherapy for Pediatric Brain Tumors Sayour, Elias J. Mitchell, Duane A. Brain Sci Review Malignant brain tumors are the most common cause of solid cancer death in children. New targeted therapies are vital to improve treatment outcomes, but must be developed to enable trafficking across the blood brain barrier (BBB). Since activated T cells cross the BBB, cancer immunotherapy can be harnessed to unlock the cytotoxic potential of the immune system. However, standard of care treatments (i.e., chemotherapy and radiation) applied concomitant to pediatric brain tumor immunotherapy may abrogate induction of immunotherapeutic responses. This review will discuss the development of immunotherapies within this paradigm using emerging approaches being investigated in phase I/II trials in children with refractory brain tumors, including checkpoint inhibitors, vaccine immunotherapy, and adoptive cell therapy. MDPI 2017-10-21 /pmc/articles/PMC5664064/ /pubmed/29065490 http://dx.doi.org/10.3390/brainsci7100137 Text en © 2017 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 | Review Sayour, Elias J. Mitchell, Duane A. Immunotherapy for Pediatric Brain Tumors |
title | Immunotherapy for Pediatric Brain Tumors |
title_full | Immunotherapy for Pediatric Brain Tumors |
title_fullStr | Immunotherapy for Pediatric Brain Tumors |
title_full_unstemmed | Immunotherapy for Pediatric Brain Tumors |
title_short | Immunotherapy for Pediatric Brain Tumors |
title_sort | immunotherapy for pediatric brain tumors |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5664064/ https://www.ncbi.nlm.nih.gov/pubmed/29065490 http://dx.doi.org/10.3390/brainsci7100137 |
work_keys_str_mv | AT sayoureliasj immunotherapyforpediatricbraintumors AT mitchellduanea immunotherapyforpediatricbraintumors |