Abstract | BACKGROUND: Agglomeration of myeloid-derived suppressor cells (MDSCs) in tumors impedes immunotherapeutic effects. Doxorubicin (DOX) is currently the most specific drug used for the selective removal of MDSCs. Here, we study the feasibility and mechanism of eliminating MDSCs by DOX to improve antigen-specific cytotoxic T lymphocyte (CTL)-killing neuroblastoma (NB) cells in vitro. METHODS: CTL and MDSC were prepared; then, CTLs, NB cells, MDSCs, and DOX were mixed and cultivated in different collocation patterns and divided into different groups. The levels of cluster of differentiation 3ζ chain (CD3ζ) and L-selectin in CTL in different groups were detected. Thereafter, the killing rate of NB cells and secretion of interleukin-2 and interferon-γ were measured and compared. RESULTS: By real-time polymerase chain reaction (PCR) and Western blot test respectively, the proliferation and killing effect of CTLs on NB cells were all inhibited by MDSC through downregulating CD3ζ (p = 0.002; p = 0.001) and L-selectin (p = 0.006; p < 0.001). However, this inhibitory effect was reversed by DOX. Significant differences were observed in the levels of interleukin-2 (p < 0.001), interferon-γ (p < 0.001), and the killing rate (p < 0.001) among the groups, except between the CTL +SK-N-SH and CTL +SK-N-SH +DOX groups (p > 0.05). CONCLUSIONS: Targeted elimination of MDSCs by DOX can improve Ag-specific CTL killing of NB cells in vitro by upregulating CD3ζ and L-selectin. This study provides a novel method to enhance the immunotherapeutic effects of NB.
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Authors | Weili Xu, Suolin Li, Meng Li, Hui Zhou, Xiaofeng Yang |
Journal | Journal of clinical laboratory analysis
(J Clin Lab Anal)
Vol. 36
Issue 1
Pg. e24158
(Jan 2022)
ISSN: 1098-2825 [Electronic] United States |
PMID | 34861064
(Publication Type: Journal Article)
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Copyright | © 2021 The Authors. Journal of Clinical Laboratory Analysis published by Wiley Periodicals LLC. |
Chemical References |
- Antineoplastic Agents
- L-Selectin
- Doxorubicin
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Topics |
- Animals
- Antineoplastic Agents
(pharmacology)
- Cell Line, Tumor
- Doxorubicin
(pharmacology)
- Humans
- L-Selectin
(genetics, metabolism)
- Mice
- Myeloid-Derived Suppressor Cells
(drug effects, metabolism)
- Neuroblastoma
(metabolism, pathology)
- T-Lymphocytes, Cytotoxic
(metabolism)
- Up-Regulation
(genetics)
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