Abstract

BackgroundDendritic cells are potent and specialized antigen presenting cells, which play a crucial role in initiating and amplifying both the innate and adaptive immune responses. The dendritic cell-based vaccination against cancer has been clinically achieved promising successes. But there are still many challenges in its clinical application, especially for how to identify the functional states.MethodsThe CD14+ monocytes were isolated from human peripheral blood after plastic adherence and purified to approximately 98% with cocktail immunomagnetic beads. The immature dendritic cells and mature dendritic cells were induced by traditional protocols. The resulting dendritic cells were cocultured with normal cells and cancer cells. The functional state of dendritic cells including immature dendritic cells (imDCs) and mature dendritic cells (mDCs) under different conditioned microenvironments were investigated by Fourier transformed infrared spectroscopy (FTIR) and molecular biological methods.ResultsThe results of Fourier transformed infrared spectroscopy showed that the gene transcription activity and energy states of dendritic cells were specifically suppressed by tumor cells (P < 0.05 or 0.01). The expression levels of NF-kappa B (NF-κB) in dendritic cells were also specifically inhibited by tumor-derived factors (P < 0.05 or 0.01). Moreover, the ratios of absorption intensities of Fourier transformed infrared spectroscopy at given wave numbers were closely correlated with the expression levels of NF-κB (R2:0.69 and R2:0.81, respectively).ConclusionOur results confirmed that the ratios of absorption intensities of Fourier transformed infrared spectroscopy at given wave numbers were positively correlated with the expression levels of NF-κB, suggesting that Fourier transformed infrared spectroscopy technology could be clinically applied to identify the functional states of dendritic cell when performing dendritic cell-based vaccination. It’s significant for the simplification and standardization of dendritic cell-based vaccination clinical preparation protocols.

Highlights

  • Dendritic cells (DCs) are potent and specialized antigen-presenting cells with the capabilities of capturing, processing antigens and presenting tumor associated antigens to naive-T cells, inducing tumor-specific immune response [1,2]

  • It was clinically cumbersome for the preparation of Dendritic cells-based vaccination (DCBV) and difficult to determine the functional state of DCs

  • The results showed that the gene transcription activity and energy states of DCs were suppressed by tumor cells, the absorption intensities of Fourier transformed infrared spectroscopy (FTIR) at given wave number were closely correlated with the expression levels of RelB

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Summary

Introduction

Dendritic cells (DCs) are potent and specialized antigen-presenting cells with the capabilities of capturing, processing antigens and presenting tumor associated antigens to naive-T cells, inducing tumor-specific immune response [1,2]. There are still many challenges in clinical application of DCBV, such as antigen selection, ways of antigen loading, pathways and intervals of injection, and identification of the functional state of DCs [3,4,5,6]. Many strategies have been focused on the improvement of the efficiency of DCBV [1,5,7], little about identification of functional state of cells. It was clinically cumbersome for the preparation of DCBV and difficult to determine the functional state of DCs. how to measure the functional state of DCs with a convenient, reliable and non-invasive method is practically for DCBV preparation protocols. The functional state of dendritic cells including immature dendritic cells (imDCs) and mature dendritic cells (mDCs) under different conditioned microenvironments were investigated by Fourier transformed infrared spectroscopy (FTIR) and molecular biological methods

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