Document Type : Original Article

Authors

1 Department of Immunology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.

2 Nervous System Stem Cells Research Center, Semnan University of Medical Sciences, Semnan, Iran.

3 Department of Tissue Engineering and Applied Cell Sciences, School of Medicine, Semnan University of Medical Sciences, Semnan, Iran.

4 Department of Immunology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.

5 Allergy Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.

6 Department of Electrical Engineering, Faculty of Engineering, University of Zanjan, Zanjan, Iran.

7 Department of Pathobiology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.

8 Laboratory of Signals and Electronic Systems, Faculty of electrical and computer Engineering, Khajeh Nasir Toosi University of Technology, Tehran, Iran.

9 Division of Imaging Sciences and Biomedical Engineering, St Thomas’ Hospital, Faculty of Life Sciences and Medicine, King’s College London, London, England.

10 Cancer Biology Research Center, Cancer Institute of Iran, Tehran University of Medical Sciences, Tehran, Iran.

10.22034/iji.2022.91617.2092

Abstract

Background: Mathematical modeling offers the possibility to select the optimal dose of a drug or vaccine. Considerable evidence show that many bacterial components can activate dendritic cells (DCs). Our previous report showed that multiple doses of DCs matured with Listeria monocytogenes led to tumor regression whereas multiple doses of CpG-matured DCs affected tumor reversely. Objective: To assess a combined pattern of DC vaccination proposed by a mathematical model for tumor regression. Method: WEHI164 cells were inoculated subcutaneously in the right flank of BALB/c mice. Bone marrow-derived DCs were matured by Listeria monocytogenes and CpG motifs. DCs were injected using specific patterns and doses predicted by mathematical modeling. Effector cell-mediated cytotoxicity, gene expression of T cell-related transcription factors, as well as tumor growth and survival rate, were assessed in different groups. Results: Our study indicated that the proposed mathematical model could simulate the tumor and immune system interaction, and it was verified by decreasing tumor size in the List+CpG group. However, comparing the effect of different treatment modalities on Th1/Treg transcription factor expression or cytotoxic responses revealed no advantage for combined therapy over other treatment modalities. Conclusions: These results suggest that finding new combinations of DC vaccines for the treatment of tumors will be promising in the future. The results of this study support the mathematical modelling for DC vaccine design. However, some parameters in this model must be modified to provide a more optimized therapy approach.

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