Lenalidomide Enhances CAR-T Cell Activity Against Solid Tumor Cells
Author(s) -
Zhixiong Wang,
Zhou Guo-min,
Risu Na,
Jiayu Fu,
Yan Zou,
Jiaxing Tang,
Long Li,
Hui Liu,
Qian Liu,
Xuekai Zhu
Publication year - 2020
Publication title -
cell transplantation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.043
H-Index - 100
eISSN - 1555-3892
pISSN - 0963-6897
DOI - 10.1177/0963689720920825
Subject(s) - lenalidomide , chimeric antigen receptor , cytokine , cytotoxicity , cancer research , t cell , cell culture , cell growth , cancer immunotherapy , chemistry , immunotherapy , biology , microbiology and biotechnology , immunology , immune system , multiple myeloma , in vitro , biochemistry , genetics
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.
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