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Chimeric Antigen Receptor (CAR)-T Cell Immunotherapy Against Thoracic Malignancies: Challenges and Opportunities

Different from surgery, chemical therapy, radio-therapy and target therapy, Chimeric antigen receptor-modified T (CAR-T) cells, a novel adoptive immunotherapy strategy, have been used successfully against both hematological tumors and solid tumors. Although several problems have reduced engineered C...

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Autores principales: Chen, Long, Chen, Fukun, Niu, Huatao, Li, Jindan, Pu, Yongzhu, Yang, Conghui, Wang, Yue, Huang, Rong, Li, Ke, Lei, Yujie, Huang, Yunchao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9334018/
https://www.ncbi.nlm.nih.gov/pubmed/35911706
http://dx.doi.org/10.3389/fimmu.2022.871661
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author Chen, Long
Chen, Fukun
Niu, Huatao
Li, Jindan
Pu, Yongzhu
Yang, Conghui
Wang, Yue
Huang, Rong
Li, Ke
Lei, Yujie
Huang, Yunchao
author_facet Chen, Long
Chen, Fukun
Niu, Huatao
Li, Jindan
Pu, Yongzhu
Yang, Conghui
Wang, Yue
Huang, Rong
Li, Ke
Lei, Yujie
Huang, Yunchao
author_sort Chen, Long
collection PubMed
description Different from surgery, chemical therapy, radio-therapy and target therapy, Chimeric antigen receptor-modified T (CAR-T) cells, a novel adoptive immunotherapy strategy, have been used successfully against both hematological tumors and solid tumors. Although several problems have reduced engineered CAR-T cell therapeutic outcomes in clinical trials for the treatment of thoracic malignancies, including the lack of specific antigens, an immunosuppressive tumor microenvironment, a low level of CAR-T cell infiltration into tumor tissues, off-target toxicity, and other safety issues, CAR-T cell treatment is still full of bright future. In this review, we outline the basic structure and characteristics of CAR-T cells among different period, summarize the common tumor-associated antigens in clinical trials of CAR-T cell therapy for thoracic malignancies, and point out the current challenges and new strategies, aiming to provide new ideas and approaches for preclinical experiments and clinical trials of CAR-T cell therapy for thoracic malignancies.
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spelling pubmed-93340182022-07-29 Chimeric Antigen Receptor (CAR)-T Cell Immunotherapy Against Thoracic Malignancies: Challenges and Opportunities Chen, Long Chen, Fukun Niu, Huatao Li, Jindan Pu, Yongzhu Yang, Conghui Wang, Yue Huang, Rong Li, Ke Lei, Yujie Huang, Yunchao Front Immunol Immunology Different from surgery, chemical therapy, radio-therapy and target therapy, Chimeric antigen receptor-modified T (CAR-T) cells, a novel adoptive immunotherapy strategy, have been used successfully against both hematological tumors and solid tumors. Although several problems have reduced engineered CAR-T cell therapeutic outcomes in clinical trials for the treatment of thoracic malignancies, including the lack of specific antigens, an immunosuppressive tumor microenvironment, a low level of CAR-T cell infiltration into tumor tissues, off-target toxicity, and other safety issues, CAR-T cell treatment is still full of bright future. In this review, we outline the basic structure and characteristics of CAR-T cells among different period, summarize the common tumor-associated antigens in clinical trials of CAR-T cell therapy for thoracic malignancies, and point out the current challenges and new strategies, aiming to provide new ideas and approaches for preclinical experiments and clinical trials of CAR-T cell therapy for thoracic malignancies. Frontiers Media S.A. 2022-07-14 /pmc/articles/PMC9334018/ /pubmed/35911706 http://dx.doi.org/10.3389/fimmu.2022.871661 Text en Copyright © 2022 Chen, Chen, Niu, Li, Pu, Yang, Wang, Huang, Li, Lei and Huang 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
Chen, Long
Chen, Fukun
Niu, Huatao
Li, Jindan
Pu, Yongzhu
Yang, Conghui
Wang, Yue
Huang, Rong
Li, Ke
Lei, Yujie
Huang, Yunchao
Chimeric Antigen Receptor (CAR)-T Cell Immunotherapy Against Thoracic Malignancies: Challenges and Opportunities
title Chimeric Antigen Receptor (CAR)-T Cell Immunotherapy Against Thoracic Malignancies: Challenges and Opportunities
title_full Chimeric Antigen Receptor (CAR)-T Cell Immunotherapy Against Thoracic Malignancies: Challenges and Opportunities
title_fullStr Chimeric Antigen Receptor (CAR)-T Cell Immunotherapy Against Thoracic Malignancies: Challenges and Opportunities
title_full_unstemmed Chimeric Antigen Receptor (CAR)-T Cell Immunotherapy Against Thoracic Malignancies: Challenges and Opportunities
title_short Chimeric Antigen Receptor (CAR)-T Cell Immunotherapy Against Thoracic Malignancies: Challenges and Opportunities
title_sort chimeric antigen receptor (car)-t cell immunotherapy against thoracic malignancies: challenges and opportunities
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9334018/
https://www.ncbi.nlm.nih.gov/pubmed/35911706
http://dx.doi.org/10.3389/fimmu.2022.871661
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