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Anti-CD166/4-1BB chimeric antigen receptor T cell therapy for the treatment of osteosarcoma

BACKGROUND: Chimeric antigen receptor (CAR)-engineered T cells have displayed outstanding performance in the treatment of patients with hematological malignancies. However, their efficacy against solid tumors has been largely limited. METHODS: In this study, human osteosarcoma cell lines were prepar...

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Autores principales: Wang, Yitian, Yu, Wei, Zhu, Jian, Wang, Junjie, Xia, Kaishun, Liang, Chengzhen, Tao, Huimin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6471997/
https://www.ncbi.nlm.nih.gov/pubmed/30995926
http://dx.doi.org/10.1186/s13046-019-1147-6
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author Wang, Yitian
Yu, Wei
Zhu, Jian
Wang, Junjie
Xia, Kaishun
Liang, Chengzhen
Tao, Huimin
author_facet Wang, Yitian
Yu, Wei
Zhu, Jian
Wang, Junjie
Xia, Kaishun
Liang, Chengzhen
Tao, Huimin
author_sort Wang, Yitian
collection PubMed
description BACKGROUND: Chimeric antigen receptor (CAR)-engineered T cells have displayed outstanding performance in the treatment of patients with hematological malignancies. However, their efficacy against solid tumors has been largely limited. METHODS: In this study, human osteosarcoma cell lines were prepared, flow cytometry using antibodies against CD166 was performed on different cell samples. CD166-specific T cells were obtained by viral gene transfer of corresponding DNA plasmids and selectively expanded using IL-2 and IL-15. The ability of CD166.BBζ CAR-T cells to kill CD166(+) osteosarcoma cells was evaluated in vitro and in vivo. RESULTS: CD166 was selectively expressed on four different human osteosarcoma cell lines, indicating its role as the novel target for CAR-T cell therapy. CD166.BBζ CAR-T cells killed osteosarcoma cell lines in vitro; the cytotoxicity correlated with the level of CD166 expression on the tumor cells. Intravenous injection of CD166.BBζ CAR-T cells into mice resulted in the regression of the tumor with no obvious toxicity. CONCLUSIONS: Together, the data suggest that CD166.BBζ CAR-T cells may serve as a new therapeutic strategy in the future clinical practice for the treatment of osteosarcoma. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13046-019-1147-6) contains supplementary material, which is available to authorized users.
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spelling pubmed-64719972019-04-24 Anti-CD166/4-1BB chimeric antigen receptor T cell therapy for the treatment of osteosarcoma Wang, Yitian Yu, Wei Zhu, Jian Wang, Junjie Xia, Kaishun Liang, Chengzhen Tao, Huimin J Exp Clin Cancer Res Research BACKGROUND: Chimeric antigen receptor (CAR)-engineered T cells have displayed outstanding performance in the treatment of patients with hematological malignancies. However, their efficacy against solid tumors has been largely limited. METHODS: In this study, human osteosarcoma cell lines were prepared, flow cytometry using antibodies against CD166 was performed on different cell samples. CD166-specific T cells were obtained by viral gene transfer of corresponding DNA plasmids and selectively expanded using IL-2 and IL-15. The ability of CD166.BBζ CAR-T cells to kill CD166(+) osteosarcoma cells was evaluated in vitro and in vivo. RESULTS: CD166 was selectively expressed on four different human osteosarcoma cell lines, indicating its role as the novel target for CAR-T cell therapy. CD166.BBζ CAR-T cells killed osteosarcoma cell lines in vitro; the cytotoxicity correlated with the level of CD166 expression on the tumor cells. Intravenous injection of CD166.BBζ CAR-T cells into mice resulted in the regression of the tumor with no obvious toxicity. CONCLUSIONS: Together, the data suggest that CD166.BBζ CAR-T cells may serve as a new therapeutic strategy in the future clinical practice for the treatment of osteosarcoma. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13046-019-1147-6) contains supplementary material, which is available to authorized users. BioMed Central 2019-04-17 /pmc/articles/PMC6471997/ /pubmed/30995926 http://dx.doi.org/10.1186/s13046-019-1147-6 Text en © The Author(s). 2019 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 Research
Wang, Yitian
Yu, Wei
Zhu, Jian
Wang, Junjie
Xia, Kaishun
Liang, Chengzhen
Tao, Huimin
Anti-CD166/4-1BB chimeric antigen receptor T cell therapy for the treatment of osteosarcoma
title Anti-CD166/4-1BB chimeric antigen receptor T cell therapy for the treatment of osteosarcoma
title_full Anti-CD166/4-1BB chimeric antigen receptor T cell therapy for the treatment of osteosarcoma
title_fullStr Anti-CD166/4-1BB chimeric antigen receptor T cell therapy for the treatment of osteosarcoma
title_full_unstemmed Anti-CD166/4-1BB chimeric antigen receptor T cell therapy for the treatment of osteosarcoma
title_short Anti-CD166/4-1BB chimeric antigen receptor T cell therapy for the treatment of osteosarcoma
title_sort anti-cd166/4-1bb chimeric antigen receptor t cell therapy for the treatment of osteosarcoma
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6471997/
https://www.ncbi.nlm.nih.gov/pubmed/30995926
http://dx.doi.org/10.1186/s13046-019-1147-6
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