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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...

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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
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
Descripción
Sumario: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.