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The Chemokine Receptor CCR8 Is a Target of Chimeric Antigen T Cells for Treating T Cell Malignancies
Chimeric antigen receptor (CAR) T cells have been successfully used in the therapy of B cell leukemia and lymphoma, but still have many challenges in their use for treating T cell malignancies, such as the lack of unique tumor antigens, their limitation of T cell expansion, and the need for third pa...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9182403/ https://www.ncbi.nlm.nih.gov/pubmed/35693763 http://dx.doi.org/10.3389/fimmu.2022.808347 |
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author | Zheng, Diwei Wang, Xindong Cheng, Lin Qin, Le Jiang, Zhiwu Zhao, Ruocong Li, Yao Shi, Jingxuan Wu, Qiting Long, Youguo Wang, Suna Tang, Zhaoyang Wei, Wei Yang, Jie Li, Yangqiu Zhou, Hongsheng Liu, Qifa Liu, Pentao Chen, Xinwen Yao, Yao Yang, LiHua Li, Peng |
author_facet | Zheng, Diwei Wang, Xindong Cheng, Lin Qin, Le Jiang, Zhiwu Zhao, Ruocong Li, Yao Shi, Jingxuan Wu, Qiting Long, Youguo Wang, Suna Tang, Zhaoyang Wei, Wei Yang, Jie Li, Yangqiu Zhou, Hongsheng Liu, Qifa Liu, Pentao Chen, Xinwen Yao, Yao Yang, LiHua Li, Peng |
author_sort | Zheng, Diwei |
collection | PubMed |
description | Chimeric antigen receptor (CAR) T cells have been successfully used in the therapy of B cell leukemia and lymphoma, but still have many challenges in their use for treating T cell malignancies, such as the lack of unique tumor antigens, their limitation of T cell expansion, and the need for third party donors or genome editing. Therefore, we need to find novel targets for CAR T cell therapy to overcome these challenges. Here, we found that both adult T-cell leukemia/lymphoma (ATLL) patients and ATLL cells had increased CCR8 expression but did not express CD7. Moreover, targeting CCR8 in T cells did not impair T cell expansion in vitro. Importantly, anti-CCR8 CAR T cells exhibited antitumor effects on ATLL- and other CCR8-expressing T-ALL cells in vitro and in vivo, and prolonged the survival of ATLL and Jurkat tumor-bearing mouse models. In conclusion, these collective results show that anti-CCR8 CAR T cells possess strong antitumor activity and represent a promising therapeutic approach for ATLL and CCR8(+) tumors. |
format | Online Article Text |
id | pubmed-9182403 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-91824032022-06-10 The Chemokine Receptor CCR8 Is a Target of Chimeric Antigen T Cells for Treating T Cell Malignancies Zheng, Diwei Wang, Xindong Cheng, Lin Qin, Le Jiang, Zhiwu Zhao, Ruocong Li, Yao Shi, Jingxuan Wu, Qiting Long, Youguo Wang, Suna Tang, Zhaoyang Wei, Wei Yang, Jie Li, Yangqiu Zhou, Hongsheng Liu, Qifa Liu, Pentao Chen, Xinwen Yao, Yao Yang, LiHua Li, Peng Front Immunol Immunology Chimeric antigen receptor (CAR) T cells have been successfully used in the therapy of B cell leukemia and lymphoma, but still have many challenges in their use for treating T cell malignancies, such as the lack of unique tumor antigens, their limitation of T cell expansion, and the need for third party donors or genome editing. Therefore, we need to find novel targets for CAR T cell therapy to overcome these challenges. Here, we found that both adult T-cell leukemia/lymphoma (ATLL) patients and ATLL cells had increased CCR8 expression but did not express CD7. Moreover, targeting CCR8 in T cells did not impair T cell expansion in vitro. Importantly, anti-CCR8 CAR T cells exhibited antitumor effects on ATLL- and other CCR8-expressing T-ALL cells in vitro and in vivo, and prolonged the survival of ATLL and Jurkat tumor-bearing mouse models. In conclusion, these collective results show that anti-CCR8 CAR T cells possess strong antitumor activity and represent a promising therapeutic approach for ATLL and CCR8(+) tumors. Frontiers Media S.A. 2022-05-26 /pmc/articles/PMC9182403/ /pubmed/35693763 http://dx.doi.org/10.3389/fimmu.2022.808347 Text en Copyright © 2022 Zheng, Wang, Cheng, Qin, Jiang, Zhao, Li, Shi, Wu, Long, Wang, Tang, Wei, Yang, Li, Zhou, Liu, Liu, Chen, Yao, Yang and Li 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 Zheng, Diwei Wang, Xindong Cheng, Lin Qin, Le Jiang, Zhiwu Zhao, Ruocong Li, Yao Shi, Jingxuan Wu, Qiting Long, Youguo Wang, Suna Tang, Zhaoyang Wei, Wei Yang, Jie Li, Yangqiu Zhou, Hongsheng Liu, Qifa Liu, Pentao Chen, Xinwen Yao, Yao Yang, LiHua Li, Peng The Chemokine Receptor CCR8 Is a Target of Chimeric Antigen T Cells for Treating T Cell Malignancies |
title | The Chemokine Receptor CCR8 Is a Target of Chimeric Antigen T Cells for Treating T Cell Malignancies |
title_full | The Chemokine Receptor CCR8 Is a Target of Chimeric Antigen T Cells for Treating T Cell Malignancies |
title_fullStr | The Chemokine Receptor CCR8 Is a Target of Chimeric Antigen T Cells for Treating T Cell Malignancies |
title_full_unstemmed | The Chemokine Receptor CCR8 Is a Target of Chimeric Antigen T Cells for Treating T Cell Malignancies |
title_short | The Chemokine Receptor CCR8 Is a Target of Chimeric Antigen T Cells for Treating T Cell Malignancies |
title_sort | chemokine receptor ccr8 is a target of chimeric antigen t cells for treating t cell malignancies |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9182403/ https://www.ncbi.nlm.nih.gov/pubmed/35693763 http://dx.doi.org/10.3389/fimmu.2022.808347 |
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