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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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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. |
format | Online Article Text |
id | pubmed-6471997 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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