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Published in: Cancer Cell International 1/2022

Open Access 01-12-2022 | Metastasis | Primary research

CD40 monoclonal antibody and OK432 synergistically promote the activation of dendritic cells in immunotherapy

Authors: Juan Zhang, Lei Wang, Shuyi Li, Xuefeng Gao, Zhong Liu

Published in: Cancer Cell International | Issue 1/2022

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Abstract

Background

Colorectal cancer (CRC) with pulmonary metastasis usually indicates a poor prognosis, whereas patients may benefit from adoptive cell therapy. Tumor-specific cytotoxic T lymphocytes (CTLs) have been reported as a promising treatment for CRC. However, the antitumor effect of CTLs remains limited partially due to insufficient production of effector cells via the activation by antigen-presenting dendritic cells (DCs).

Method

This study showed that a combination of CD40 mAb and Picibanil (OK-432) could significantly enhance the activation of CTLs by DCs, both in vitro and in vivo. Flow cytometry, colon cancer mouse model, and pathological staining were employed to demonstrate the specific functions.

Results

This approach promoted the maturation of DCs, augmented the production of stimulatory cytokines, and suppressed the secretion of inhibitory cytokines. Additionally, it facilitated the killing efficiency of CTLs via stimulating their proliferation while restraining the number of Tregs, concomitantly with the positive regulation of corresponding cytokines. Furthermore, the combined unit could hurdle the expansion of tumor cells on metastatic lungs in the colon cancer mouse model.

Conclusion

Collectively, the combination of CD40-mAb and OK-432 facilitated the maturation of DCs and enhanced the cytotoxicity of T cells, promising therapeutic approach against CRC.

Graphical Abstract

Appendix
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Metadata
Title
CD40 monoclonal antibody and OK432 synergistically promote the activation of dendritic cells in immunotherapy
Authors
Juan Zhang
Lei Wang
Shuyi Li
Xuefeng Gao
Zhong Liu
Publication date
01-12-2022
Publisher
BioMed Central
Published in
Cancer Cell International / Issue 1/2022
Electronic ISSN: 1475-2867
DOI
https://doi.org/10.1186/s12935-022-02630-x

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