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Lenalidomide Enhances CAR-T Cell Activity Against Solid Tumor Cells
Chimeric antigen receptor (CAR) T-cell immunotherapy still faces many challenges in the treatment of solid tumors, one of which is T-cell dysfunction or exhaustion. Immunomodulator lenalidomide may improve CAR T-cell function. In this study, the effects of lenalidomide on CAR T-cell functions (cytot...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7784582/ https://www.ncbi.nlm.nih.gov/pubmed/32967454 http://dx.doi.org/10.1177/0963689720920825 |
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author | Wang, Zhixiong Zhou, Guomin Risu, Na Fu, Jiayu Zou, Yan Tang, Jiaxing Li, Long Liu, Hui Liu, Qian Zhu, Xuekai |
author_facet | Wang, Zhixiong Zhou, Guomin Risu, Na Fu, Jiayu Zou, Yan Tang, Jiaxing Li, Long Liu, Hui Liu, Qian Zhu, Xuekai |
author_sort | Wang, Zhixiong |
collection | PubMed |
description | Chimeric antigen receptor (CAR) T-cell immunotherapy still faces many challenges in the treatment of solid tumors, one of which is T-cell dysfunction or exhaustion. Immunomodulator lenalidomide may improve CAR T-cell function. In this study, the effects of lenalidomide on CAR T-cell functions (cytotoxicity, cytokine secretion, and cell proliferation) were investigated. Two different CAR T cells (CD133-specific CAR and HER2-specific CAR) were prepared, and the corresponding target cells including human glioma cell line U251 CD133-OE that overexpress CD133 and human breast cancer cell line MDA-MB-453 were used for functional assay. We found that lenalidomide promoted the killing of U251 CD133-OE by CD133-CAR T cells, the cytokine secretion, and the proliferation of CD133-CAR T cells. Lenalidomide also enhanced the cytotoxicity against MDA-MB-453 and the cytokine secretion of HER2-CAR T cells but did not affect their proliferation significantly. Furthermore, lenalidomide may regulate the function of CAR T cells by inducing the degradation of transcription factors Ikaros and Aiolos. |
format | Online Article Text |
id | pubmed-7784582 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-77845822021-01-14 Lenalidomide Enhances CAR-T Cell Activity Against Solid Tumor Cells Wang, Zhixiong Zhou, Guomin Risu, Na Fu, Jiayu Zou, Yan Tang, Jiaxing Li, Long Liu, Hui Liu, Qian Zhu, Xuekai Cell Transplant Cancer Pharmacogenomics and Target Therapy Chimeric antigen receptor (CAR) T-cell immunotherapy still faces many challenges in the treatment of solid tumors, one of which is T-cell dysfunction or exhaustion. Immunomodulator lenalidomide may improve CAR T-cell function. In this study, the effects of lenalidomide on CAR T-cell functions (cytotoxicity, cytokine secretion, and cell proliferation) were investigated. Two different CAR T cells (CD133-specific CAR and HER2-specific CAR) were prepared, and the corresponding target cells including human glioma cell line U251 CD133-OE that overexpress CD133 and human breast cancer cell line MDA-MB-453 were used for functional assay. We found that lenalidomide promoted the killing of U251 CD133-OE by CD133-CAR T cells, the cytokine secretion, and the proliferation of CD133-CAR T cells. Lenalidomide also enhanced the cytotoxicity against MDA-MB-453 and the cytokine secretion of HER2-CAR T cells but did not affect their proliferation significantly. Furthermore, lenalidomide may regulate the function of CAR T cells by inducing the degradation of transcription factors Ikaros and Aiolos. SAGE Publications 2020-09-24 /pmc/articles/PMC7784582/ /pubmed/32967454 http://dx.doi.org/10.1177/0963689720920825 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Cancer Pharmacogenomics and Target Therapy Wang, Zhixiong Zhou, Guomin Risu, Na Fu, Jiayu Zou, Yan Tang, Jiaxing Li, Long Liu, Hui Liu, Qian Zhu, Xuekai Lenalidomide Enhances CAR-T Cell Activity Against Solid Tumor Cells |
title | Lenalidomide Enhances CAR-T Cell Activity Against Solid Tumor Cells |
title_full | Lenalidomide Enhances CAR-T Cell Activity Against Solid Tumor Cells |
title_fullStr | Lenalidomide Enhances CAR-T Cell Activity Against Solid Tumor Cells |
title_full_unstemmed | Lenalidomide Enhances CAR-T Cell Activity Against Solid Tumor Cells |
title_short | Lenalidomide Enhances CAR-T Cell Activity Against Solid Tumor Cells |
title_sort | lenalidomide enhances car-t cell activity against solid tumor cells |
topic | Cancer Pharmacogenomics and Target Therapy |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7784582/ https://www.ncbi.nlm.nih.gov/pubmed/32967454 http://dx.doi.org/10.1177/0963689720920825 |
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