Abstract

Myeloid-derived suppressor cells (MDSCs) are present in the human lung microenvironment, and they may be involved in the local inflammatory process in chronic obstructive pulmonary disease (COPD). Chronic inflammation in COPD may induce immunogenic cell death of structural airway cells, causing the release of damage-associated molecular patterns (DAMPs). DAMPs may activate the innate and adaptive immune system. The relationship between MDSCs and DAMPs in COPD is poorly described in the available literature. Objectives. (1) Assessment of MDSC percentage and DAMP concentration in bronchoalveolar lavage fluid (BALF) and peripheral blood. (2) Analysis of the relationship between MDSC percentage and chosen DAMPs. Patients and Methods. 30 COPD patients were included. Using monoclonal antibodies directly conjugated with fluorochromes in flow cytometry, MDSCs were assessed in BALF and peripheral blood. The concentration of DAMPs was estimated using sandwich ELISA. Using the Bradford method, the total protein concentrations were evaluated. Results. The percentage of MDSCs among MC in BALF correlated well with the concentration of defensin and heat shock protein 27. Assessing the percentage of MDSCs among all leukocytes in BALF, we revealed a significant correlation with the concentration of defensin, hyaluronic acid, and surfactant protein A. No dependencies occurred between DAMPs and MDSCs in peripheral blood. Conclusion. MDSCs and DAMPs occur in the COPD patient lung microenvironment. Significant correlations between them found in BALF may indicate their influence on the local inflammatory process in COPD. These relationships allow better understanding of the inflammatory process in COPD.

Highlights

  • Chronic obstructive pulmonary disease (COPD) is a significant cause of death in the world

  • Assessing the percentage of Myeloid-derived suppressor cells (MDSCs) among all leukocytes in bronchoalveolar lavage fluid (BALF), we revealed a significant correlation with the concentration of defensin, hyaluronic acid, and surfactant protein A

  • We revealed a significant correlation with BALF DEF/total protein (TP) (see Figure 2(c)), BALF hyaluronic acid (HA)/TP (see Figure 2(d)), and BALF Surfactant protein A (SP-A)/TP (see Figure 2(e)), assessing the percentage of MDSCs among all leukocytes

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Summary

Introduction

Chronic obstructive pulmonary disease (COPD) is a significant cause of death in the world. The adaptive immune system is activated in COPD, as defined by lung infiltration of CD8 T cells, B cells, and both the Th 17 and Th 1 types of CD4 T cells, along with a decrease in regulatory T cells in the airways [3]. These cells release soluble inflammatory agents, which interact with structural cells in the airways, lung parenchyma, and pulmonary vasculature. Various mediators that are increased in COPD patients attract the inflammatory cells from the circulation (chemoattractants)

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