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Adoptive Cell Therapy in Pediatric and Young Adult Solid Tumors: Current Status and Future Directions

Advances from novel adoptive cellular therapies have yet to be fully realized for the treatment of children and young adults with solid tumors. This review discusses the strategies and preliminary results, including T-cell, NK-cell and myeloid cell-based therapies. While each of these approaches hav...

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Autores principales: Ligon, John A., Wessel, Kristin M., Shah, Nirali N., Glod, John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8901720/
https://www.ncbi.nlm.nih.gov/pubmed/35273619
http://dx.doi.org/10.3389/fimmu.2022.846346
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author Ligon, John A.
Wessel, Kristin M.
Shah, Nirali N.
Glod, John
author_facet Ligon, John A.
Wessel, Kristin M.
Shah, Nirali N.
Glod, John
author_sort Ligon, John A.
collection PubMed
description Advances from novel adoptive cellular therapies have yet to be fully realized for the treatment of children and young adults with solid tumors. This review discusses the strategies and preliminary results, including T-cell, NK-cell and myeloid cell-based therapies. While each of these approaches have shown some early promise, there remain challenges. These include poor trafficking to the tumor as well as a hostile tumor microenvironment with numerous immunosuppressive mechanisms which result in exhaustion of cellular therapies. We then turn our attention to new strategies proposed to address these challenges including novel clinical trials that are ongoing and in development.
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spelling pubmed-89017202022-03-09 Adoptive Cell Therapy in Pediatric and Young Adult Solid Tumors: Current Status and Future Directions Ligon, John A. Wessel, Kristin M. Shah, Nirali N. Glod, John Front Immunol Immunology Advances from novel adoptive cellular therapies have yet to be fully realized for the treatment of children and young adults with solid tumors. This review discusses the strategies and preliminary results, including T-cell, NK-cell and myeloid cell-based therapies. While each of these approaches have shown some early promise, there remain challenges. These include poor trafficking to the tumor as well as a hostile tumor microenvironment with numerous immunosuppressive mechanisms which result in exhaustion of cellular therapies. We then turn our attention to new strategies proposed to address these challenges including novel clinical trials that are ongoing and in development. Frontiers Media S.A. 2022-02-22 /pmc/articles/PMC8901720/ /pubmed/35273619 http://dx.doi.org/10.3389/fimmu.2022.846346 Text en Copyright © 2022 Ligon, Wessel, Shah and Glod 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
Ligon, John A.
Wessel, Kristin M.
Shah, Nirali N.
Glod, John
Adoptive Cell Therapy in Pediatric and Young Adult Solid Tumors: Current Status and Future Directions
title Adoptive Cell Therapy in Pediatric and Young Adult Solid Tumors: Current Status and Future Directions
title_full Adoptive Cell Therapy in Pediatric and Young Adult Solid Tumors: Current Status and Future Directions
title_fullStr Adoptive Cell Therapy in Pediatric and Young Adult Solid Tumors: Current Status and Future Directions
title_full_unstemmed Adoptive Cell Therapy in Pediatric and Young Adult Solid Tumors: Current Status and Future Directions
title_short Adoptive Cell Therapy in Pediatric and Young Adult Solid Tumors: Current Status and Future Directions
title_sort adoptive cell therapy in pediatric and young adult solid tumors: current status and future directions
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8901720/
https://www.ncbi.nlm.nih.gov/pubmed/35273619
http://dx.doi.org/10.3389/fimmu.2022.846346
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