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Engineering CAR T cells for enhanced efficacy and safety

Despite its success in treating hematologic malignancies, chimeric antigen receptor (CAR) T cell therapy faces two major challenges which hinder its broader applications: the limited effectiveness against solid tumors and the nonspecific toxicities. To address these concerns, researchers have used s...

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Detalles Bibliográficos
Autores principales: Wu, Yiqian, Huang, Ziliang, Harrison, Reed, Liu, Longwei, Zhu, Linshan, Situ, Yinglin, Wang, Yingxiao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AIP Publishing LLC 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8769768/
https://www.ncbi.nlm.nih.gov/pubmed/35071966
http://dx.doi.org/10.1063/5.0073746
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author Wu, Yiqian
Huang, Ziliang
Harrison, Reed
Liu, Longwei
Zhu, Linshan
Situ, Yinglin
Wang, Yingxiao
author_facet Wu, Yiqian
Huang, Ziliang
Harrison, Reed
Liu, Longwei
Zhu, Linshan
Situ, Yinglin
Wang, Yingxiao
author_sort Wu, Yiqian
collection PubMed
description Despite its success in treating hematologic malignancies, chimeric antigen receptor (CAR) T cell therapy faces two major challenges which hinder its broader applications: the limited effectiveness against solid tumors and the nonspecific toxicities. To address these concerns, researchers have used synthetic biology approaches to develop optimization strategies. In this review, we discuss recent improvements on the CAR and other non-CAR molecules aimed to enhance CAR T cell efficacy and safety. We also highlight the development of different types of inducible CAR T cells that can be controlled by environmental cues and/or external stimuli. These advancements are bringing CAR T therapy one step closer to safer and wider applications, especially for solid tumors.
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spelling pubmed-87697682022-01-21 Engineering CAR T cells for enhanced efficacy and safety Wu, Yiqian Huang, Ziliang Harrison, Reed Liu, Longwei Zhu, Linshan Situ, Yinglin Wang, Yingxiao APL Bioeng Reviews Despite its success in treating hematologic malignancies, chimeric antigen receptor (CAR) T cell therapy faces two major challenges which hinder its broader applications: the limited effectiveness against solid tumors and the nonspecific toxicities. To address these concerns, researchers have used synthetic biology approaches to develop optimization strategies. In this review, we discuss recent improvements on the CAR and other non-CAR molecules aimed to enhance CAR T cell efficacy and safety. We also highlight the development of different types of inducible CAR T cells that can be controlled by environmental cues and/or external stimuli. These advancements are bringing CAR T therapy one step closer to safer and wider applications, especially for solid tumors. AIP Publishing LLC 2022-01-18 /pmc/articles/PMC8769768/ /pubmed/35071966 http://dx.doi.org/10.1063/5.0073746 Text en © 2022 Author(s). https://creativecommons.org/licenses/by/4.0/All article content, except where otherwise noted, is licensed under a Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ).
spellingShingle Reviews
Wu, Yiqian
Huang, Ziliang
Harrison, Reed
Liu, Longwei
Zhu, Linshan
Situ, Yinglin
Wang, Yingxiao
Engineering CAR T cells for enhanced efficacy and safety
title Engineering CAR T cells for enhanced efficacy and safety
title_full Engineering CAR T cells for enhanced efficacy and safety
title_fullStr Engineering CAR T cells for enhanced efficacy and safety
title_full_unstemmed Engineering CAR T cells for enhanced efficacy and safety
title_short Engineering CAR T cells for enhanced efficacy and safety
title_sort engineering car t cells for enhanced efficacy and safety
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8769768/
https://www.ncbi.nlm.nih.gov/pubmed/35071966
http://dx.doi.org/10.1063/5.0073746
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