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Incorporation of functional elements enhances the antitumor capacity of CAR T cells

As chimeric antigen receptor (CAR) T cells have displayed an unprecedented efficacy in the treatment of CD19-positive malignances, it is believed that this cell therapy will be a milestone in the history of mankind’s conquering of cancer. However, there are some issues that restrict CAR T cells from...

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Detalles Bibliográficos
Autores principales: Qin, Le, Zhao, Ruocong, Li, Peng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5637271/
https://www.ncbi.nlm.nih.gov/pubmed/29046826
http://dx.doi.org/10.1186/s40164-017-0088-z
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author Qin, Le
Zhao, Ruocong
Li, Peng
author_facet Qin, Le
Zhao, Ruocong
Li, Peng
author_sort Qin, Le
collection PubMed
description As chimeric antigen receptor (CAR) T cells have displayed an unprecedented efficacy in the treatment of CD19-positive malignances, it is believed that this cell therapy will be a milestone in the history of mankind’s conquering of cancer. However, there are some issues that restrict CAR T cells from reaching their optimal anti-tumor capacity, especially in the treatment of solid tumors. Inhibitory cytokines, immune checkpoint molecules, hypoxia and other adverse factors have been reported to be involved in this process. To obtain better efficacy in the treatment of leukemia and solid tumors, we need to continuously upgrade CAR T cell technology by incorporating novel functional elements into CAR T cells to overcome these restrictions. In this review, we summarize recent advances regarding this topic.
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spelling pubmed-56372712017-10-18 Incorporation of functional elements enhances the antitumor capacity of CAR T cells Qin, Le Zhao, Ruocong Li, Peng Exp Hematol Oncol Review As chimeric antigen receptor (CAR) T cells have displayed an unprecedented efficacy in the treatment of CD19-positive malignances, it is believed that this cell therapy will be a milestone in the history of mankind’s conquering of cancer. However, there are some issues that restrict CAR T cells from reaching their optimal anti-tumor capacity, especially in the treatment of solid tumors. Inhibitory cytokines, immune checkpoint molecules, hypoxia and other adverse factors have been reported to be involved in this process. To obtain better efficacy in the treatment of leukemia and solid tumors, we need to continuously upgrade CAR T cell technology by incorporating novel functional elements into CAR T cells to overcome these restrictions. In this review, we summarize recent advances regarding this topic. BioMed Central 2017-10-11 /pmc/articles/PMC5637271/ /pubmed/29046826 http://dx.doi.org/10.1186/s40164-017-0088-z Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Qin, Le
Zhao, Ruocong
Li, Peng
Incorporation of functional elements enhances the antitumor capacity of CAR T cells
title Incorporation of functional elements enhances the antitumor capacity of CAR T cells
title_full Incorporation of functional elements enhances the antitumor capacity of CAR T cells
title_fullStr Incorporation of functional elements enhances the antitumor capacity of CAR T cells
title_full_unstemmed Incorporation of functional elements enhances the antitumor capacity of CAR T cells
title_short Incorporation of functional elements enhances the antitumor capacity of CAR T cells
title_sort incorporation of functional elements enhances the antitumor capacity of car t cells
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5637271/
https://www.ncbi.nlm.nih.gov/pubmed/29046826
http://dx.doi.org/10.1186/s40164-017-0088-z
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