Imbalance of dendritic cell co-stimulation in COPD
Respiratory Researchvolume 16, Article number: 19 (2015)
Dendritic cells (DCs) control immunity and play a role in the pathogenesis of chronic obstructive pulmonary disease (COPD). However, the expression of function-associated surface molecules on circulating DCs in COPD is unknown.
Four-colour flow cytometry was used to compare blood DC surface molecules of 54 patients with COPD (median age: 59 years; median FEV1: 38% predicted, median CAT score: 24) with two age-matched control groups with normal lung function: 21 current smokers and 21 never-smokers.
Concentrations of plasmacytoid DCs (pDCs) and myeloid DCs (mDCs) and the mDC/pDC ratio did not differ between the groups. The increased expression of BDCA-1, BDCA-3, CD86 and CCR5 on mDCs in patients with COPD did not significantly differ from smokers with normal lung function. In contrast, COPD was specifically characterised by a decreased expression of the anti-inflammatory co-stimulatory molecule PD-L1 on pDCs and an increased expression of the pro-inflammatory co-stimulatory molecule OX40 ligand (OX40L) on mDCs. These changes were not confined to patients with elevated systemic inflammation markers (leukocytes, c-reactive protein, interleukin-6, fibrinogen). The ratio of OX40L to PD-L1 expression (OX40L/PD-L1 ratio), a quantitative measure of imbalanced DC co-stimulation, correlated with the severity of pulmonary emphysema in patients with COPD.
An imbalance of DC co-stimulation might contribute to the pathogenesis of COPD.
Chronic obstructive pulmonary disease (COPD) is a chronic inflammatory disorder characterised by both local abnormalites (including a specific type of airway inflammation) and systemic abnormalities (including typical co-morbidities and various degrees of systemic inflammation) . An abnormal immune response to inhaled noxious agents is a central pathogenetic feature of COPD, leading to lymphoid follicle formation around the airways and small airway obstruction . Smoking is the most important risk factor for the development of COPD. However, less than 30% of all smokers develop COPD  and it is still unclear which specific immunologic features account for COPD development.
Dendritic cells (DCs), which can be subdivided into myeloid DCs (mDCs) and plasmacytoid DCs (pDCs), control pulmonary immune responses. DC accumulation and activation in the airways has been postulated to be a driver of COPD immunopathology [3-9]. Using an established method to analyse human bronchoalveolar lavage fluid DCs [10-13], we have shown that airway mDCs of asymptomatic smokers show a profound adaptation to cigarette smoke exposure, including a strong upregulation of antigen-recognition receptors such as CD1a, BDCA-1 or Langerin and co-stimulatory molecules such as CD86 . Of note, this upregulation was also found on airway mDCs of current smokers with COPD, but not former smokers with COPD, suggesting that these changes are related to smoke exposure, rather than the presence of COPD. In addition, this upregulation correlated with less airway obstruction, further supporting the concept that an upregulation of these markers is not related to COPD pathogenesis . Thus, the specific causes of chronic airway inflammation in COPD are still enigmatic. It has been postulated that enhanced local concentrations of chemokines contribute to the accumulation of DCs and the subsequent activation of lymphoyctes . We hypothesised that there may be additional changes of co-stimulatory molecules on circulating DCs contributing to the immune dysregulation in COPD. It was the aim of the present study, therefore, to study major co-stimulatory molecules such as programmed death ligand 1 (PD-L1) or OX40 ligand (OX40L) and other function-associated surface molecules on circulating DCs of patients with COPD for the first time, and to compare the findings with control groups of asymptomatic smokers and never-smokers.
Controls were recruited using public notices in Rostock (Germany). Patients with stable COPD were recruited at the University Hospital of Rostock (Germany). Inclusion criteria for patients with COPD were as follows: 1. doctor’s diagnosis of COPD, 2. age between 40 and 85 years, 3. smoking history of at least 5 pack years, 3. a FEV1/FVC ratio < 70% after inhalation of a short-acting beta-agonist. Former smokers were defined as subjects who quit smoking at least 4 weeks before study inclusion. Exclusion criteria for patients with COPD were: 1. presence of any malignant diseases, 2. any signs of an infection/exacerbation or any treatment with antibiotics or short-term corticosteroids within the last 4 weeks prior to enrollment. Controls were recruited using the following inclusion criteria: 1. no history of chronic respiratory diseases, 2. age between 40 and 85 years, 3. no history of smoking and no exposure to smoking partners or relatives at home (never-smoking controls) or a smoking history of at least 5 pack years and current smoking of at least 15 cigarettes per day (asymptomatic current smokers). For both control groups, exclusion criteria were as follows: 1. presence of any malignant or chronic inflammatory diseases, 2. any signs of an infection or treatment with antibiotics within the last 4 weeks prior to enrollment. The study was approved by the local ethics committee of the Ärztekammer Mecklenburg-Vorpommern, Rostock (Germany). All participants gave their written informed consent.
All participants were examined between 8 am and 12 pm. Lung function tests and blood sampling were performed on the same day. In a first step, informed consent was obtained and a structured history was taken. Subsequently, body plethysmography was performed and the diffusion capacity (DLCO) measured (Masterscreen, Jaeger, Carefusion, Hoechberg, Germany). Then, peripheral blood was taken for laboratory analyses (differential blood counts, fibrinogen, c-reactive protein, Interleukin-6 and 25-OH-Vitamin D) and for the analysis of blood DCs and T cells.
Blood dendritic cells were analysed using freshly collected EDTA blood as described [10-13], using the antibodies detailed in the Additional file 1: Table S1. Among blood cells negative/dim for lineage markers (CD3, CD14, CD16, CD19, CD20, CD56), mDCs were defined as CD11c+HLA-DR+linneg/dim cells and pDCs as CD123+HLA-DR+linneg/dim cells (Additional file 1: Figure S1). Surface molecule expression on DCs was quantified in histogram plots using isotype control antibodies to discriminate between specific and non-specific staining (Additional file 1: Figures S2 and S3). CD4-positive T cells in peripheral blood were defined as CD3+CD4+ cells, regulatory T cells (Tregs) were defined as CD3+CD4+CD25++CD127low/neg cells (Additional file 1: Table S1).
Statistical analysis was performed using SPSS Statistics (SPSS Inc., Chicago, Illinois, USA). The majority of parameters was not normally distributed. Therefore, parameters were expressed as medians (minimum – maximum). For the comparison of groups, the Mann–Whitney-U test for unrelated samples was used. Correlation analyses were performed using Spearman’s correlation coefficient. Probability values of p < 0.05 were regarded as significant. Boxplots display the median (line within the box), interquartil range (edges of the box) and extremes (vertical lines). Significant differences between the groups are marked with the p-value.
Characteristics of the participants
Twenty-one never-smokers, 21 asymptomatic current smokers and 54 patients with the diagnosis of COPD were included in the study. Characteristics of the participants are detailed in Table 1. There were no differences in age and gender distribution between the groups. There was no difference in the number of pack years (PY) between the group of asymptomatic smokers and the group of patients with COPD. Smokers displayed a higher body mass index (BMI) than never-smokers and patients with COPD. Patients with COPD displayed significantly worse lung function parameters, as compared to both control groups, with a median FEV1 of 1,0 liters (38% predicted): 14 patients were in spirometric GOLD stage II, 26 patients in spirometric GOLD stage III und 14 patients in spirometric GOLD stage IV. The median CAT (COPD Assessment Test) score in the COPD group was 24 (Table 1). One patient was treated with a long-acting beta-agonist (LABA) monotherapy, 3 patients with a long-acting muscarinergic antagonist (LAMA) monotherapy, 18 patients with a LABA/LAMA combination therapy, one with a LABA/ICS combination therapy and 30 patients with a LABA/LAMA/ICS triple therapy. Ten patients (18.5%) were treated with oral corticosteroids (OCS) and 31 patients (57.4%) with ICS (Table 1).
Markers of systemic inflammation
Blood concentrations of leukocytes, C-reactive protein (CRP) and fibrinogen were elevated compared to never-smoking controls, but did not significantly differ between asymptomatic smokers and patients with COPD (Table 2 and Additional file 1: Figure S4). In addition, there were no significant differences in the percentages of neutrophils, eosinophils and lymphocytes among blood leukocytes between asymptomatic smokers and patients with COPD (data not shown). In contrast, blood concentrations of Interleukin-6 (IL-6) were significantly higher in patients with COPD, as compared with asymptomatic smokers and never-smokers (Table 2 and Additional file 1: Figure S4). Twenty-seven patients with COPD (50%), 9 asymptomatic smokers (43%) and 1 never-smoker (5%) displayed a systemic inflammation according to the definition proposed by Agusti and colleagues  (at least two elevated parameters: leukocytes > 8.6 106/ml, c-reactive protein > 8.7 mg/l, fibrinogen > 5.18 g/l, Interleukin-6 > 2.6 pg/ml) (Table 2). Blood IL-6 concentrations (but not other markers of systemic inflammation) correlated with lung function parameters (FEV1 % predicted: r = −0.33, p = 0.015; IVC % predicted: r = −0.42, p = 0.002; MEF50 % predicted: r = −0.27, p = 0.049), the 6 minute walk test (6-MWT) distance (r = −0.51, p = 0.001), the CAT score (r = 0.34, p = 0.012) and the mMRC score (r = 0.41, p = 0.002) in patients with COPD (Additional file 1: Figure S5). There was no significant difference in the total concentration of Tregs and in the percentage of Tregs among CD4-positive T-cells in peripheral blood between the 3 groups (Additional file 1: Figure S6).
Percentages and concentrations of DCs in blood
Although the percentages of mDCs in blood were sigificantly higher in never-smokers than in smokers and patients with COPD, there were no differences in total mDC concentrations between the groups. Percentages and concentrations of pDCs did not differ between the groups (Table 3 and Figures 1 and 2). The ratio of mDCs to pDCs in peripheral blood did not differ between the groups (Table 3). DC concentrations in peripheral blood did not differ between former smokers (n = 42) and current smokers with COPD (n = 12) (data not shown). Percentages and concentrations of blood mDC did not differ between patients with systemic inflammation (n = 27) and patients without systemic inflammation (n = 27) (Figures 1 and 2). Although the percentage of pDCs was significantly lower in patients with systemic inflammation (n = 27), as compared with patients without systemic inflammation (n = 27), there was no difference in pDC concentrations between these two groups (Figures 1 and 2).
Surface molecule expression on blood DCs
Patients with COPD displayed a significantly increased expression of BDCA-1 (Figure 3A), BDCA-3 (Figure 3B), CD86 (Figure 3C) and CCR5 (Figure 3D) on mDCs, as compared with never-smoking controls. However, the expression of these markers did not differ between asymptomatic smokers and patients with COPD (Table 3). There were no differences in the expression of CD54 and PD-L1 on mDCs between the groups (Table 3). The expression of OX40-ligand (OX40L) on mDCs was significantly higher in patients with COPD than in both control groups (Table 3 and Figure 4A). In contrast, the expression of PD-L1 on pDCs was significantly lower in patients with COPD, as compared with both control groups (Table 3 and Figure 4B). Consequently, the ratio of OX40L expression on mDCs to PD-L1 expression on pDCs (OX40L/PD-L1 ratio) was significantly increased in patients with COPD, as compared with both control groups (Figure 5A). There was no significant correlation between blood Tregs (total concentrations and percentages among CD4-positive T-cells) and the OX40L expression on mDCs, PD-L1 expression on pDCs and the OX40L/PD-L1 ratio (data not shown). CD54 expression on pDCs was significantly lower in patients with COPD than in asymptomatic smokers, but did not differ between patients with COPD and never-smoking controls (Table 3).
Association with clinical parameters
There was no significant association of the mDC OX40L or pDC PD-L1 expression with anthropometric parameters, pulmonary function, the 6-MWT distance or the CAT score in patients with COPD (data not shown). There was no significant association of the OX40L/PD-L1 ratio with anthropometric parameters, the 6-MWT distance or the CAT score in patients with COPD (data not shown). In contrast, the OX40L/PD-L1 ratio correlated significantly with parameters of pulmonary emphysema such as the diffusion capacity (DLCO), the residual volume (RV) or the total lung capacity (TLC) (Figure 5B-D).
The expression of DC surface molecules did not significantly differ between current smokers (n = 12) and former smokers with COPD (n = 42)(data not shown). The expression of OX40L on mDCs, the expression of PD-L1 on pDCs and the OX40L/PD-L1 ratio did not significantly differ between patients with spirometric GOLD stages II (n = 14), III (n = 26) and IV (n = 14) (Figure 6A-C) and between current smokers (n = 12) and former smokers with COPD (n = 42)(Figure 6D-F), although the highest median OX40L/PD-L1 ratios were found in the subgroup of current smokers with COPD and in the subgroup of patients with spirometric GOLD stage IV (Figure 6C, F). Despite an increase in CCR5 expression (p = 0.044) in OCS treated patients, there were no differences in DC surface molecules expression between patients treated with OCS (n = 10) and patients not treated with OCS (n = 44). No differences in surface molecule expression was observed between patients treated with ICS (n = 31) and patients not treated with ICS (n = 23)(data not shown). Presence of systemic inflammation did not have an impact on the expression of the examined DC surface molecules. In particular, there was no significant difference in the expression of OX40L on mDCs and PD-L1 on pDCs between patients with systemic inflammation (n = 27) and patients without systemic inflammation (n = 27) (Figure 4C and D).
This is the first report showing an imbalance of DC co-stimulation in COPD. We demonstrate a specific increase in the pro-inflammatory co-stimulatory molecule OX40L on blood mDCs and a specific decrease in the anti-inflammatory co-stimulatory molecule PD-L1 on blood pDCs in COPD. In addition, we show that the OX40L/PD-L1 ratio, as a quantitative measure of this imbalance, correlates with the severity of pulmonary emphysema. Thus, the observed imbalance of DC co-stimulation might contribute to the pathogenesis of COPD.
Programmed death ligand 1 (PD-L1, also known as B7-H1), a member of the family of co-stimulatory B7 receptors, is expressed on DCs and binds to the CD28 family member PD-1 on T-cells . The interaction of PD-L1 with PD-1 has anti-inflammatory effects by inducing regulatory T cells (Tregs) and suppressing self- and allo-reactive T cells [17-19], and plays a central role in the prevention of autoimmune and chronic inflammatory diseases . PD-L1 is an important component of the anti-inflammatory functions of pDCs . T cells upregulate PD-1 on the surface following activation . The elevated expression of PD-1 on circulating CD4+ T cells in COPD  might, therefore, be related to a chronic T cell ativation in this condition. We show a decreased expression of the corresponding ligand (PD-L1) on pDCs in COPD and speculate that this defective PD-L1 expression results in a decreased ability of pDCs to control inflammation, contributing to chronic inflammation in COPD. Therefore, further studies are needed to investigate the role of the PD-L1/PD-1 axis in COPD pathogenesis.
In contrast to PD-L1, we found an increased expression of OX40L on circulating mDCs in COPD. The expression of OX40L, a costimulatory molecule of DCs binding to the OX40 receptor on T cells, has been shown to be regulated by thymic stromal lymphopoietin (TSLP) which is primarily derived from bronchial epithelial cells . A TSLP-induced stimulation of the OX40L/OX40 axis has pro-inflammatory effects . As a key driver of Th2 immune responses, TSLP has been postulated to play a major pathogenetic role in asthma . However, an increased expression of TSLP has also been found in COPD [22,24]. In addition, there is an increased OX40 expression on circulating T cells (especially CD8+ T cells) in patients with COPD . Thus, the increased OX40L expression on circulating mDCs observed in the current study suggests an upregulation of the OX40L/OX40 axis in COPD. There is an ongoing discussion on possible therapeutic implications of increased TSLP and Th2 cytokine production in COPD [26,27]. Our results suggest that the OX40L/OX40 axis might be involved in COPD pathogenesis and could represent a potential new target for COPD treatment.
In order to quantify the extent of the imbalanced expression of co-stimulatory molecules on DCs, we calculated the ratio of OX40L expression on mDCs to PD-L1 expression on pDCs (“OX40L/PD-L1 ratio”). This ratio was significantly increased in patients with COPD (as compared with both control groups) and correlated with the severity of pulmonary emphysema. These data suggest that the observed imbalance of DC co-stimulation might contribute to the complex immunopathogenesis of emphysema in COPD . In contrast, we did not find a significant correlation between the OX40L/PD-L1 ratio and circulating Tregs (CD3+CD4+CD25++CD127low/neg cells) in patients with COPD. This finding does not necessarily rule out an association between the imbalanced DC co-stimulation and altered Treg functionality in COPD as there are several methods to measure Tregs and their various subclasses and functions [21,29]. Therefore, further clinical and laboratory studies are needed to better understand the relationship between altered DC phenotypes and T cell functions in COPD.
The chemokine receptor CCR5 has been implicated in the pathogenesis of COPD . CCR5 deficiency results in a marked reduction in airway inflammation and a reduced formation of peribronchial lymphoid follicles in animal models of COPD . Here, we demonstrate that CCR5 is upregulated on blood mDCs in patients with COPD. CCR5 ligands such as CCL4 (MIP-1beta) and CCL5 (RANTES) are known to be increased in the airway wall of patients with COPD [32,33]. We hypothesise that an increased expression of CCR5 on blood mDCs and increased concentrations of CCR5 ligands in the airway wall lead to an selective accumulation of these mDCs in the airway wall. This accumulation has two possible implications. First, the local increase in mDCs could contribute to lymph follicle formation and small airway inflammation in COPD . Second, the retention of CCR5-positive mDCs in the airway wall could result in a decrease of CCR5-positive mDCs in the airway lumen. Because CCR5 plays an important role in the uptake of microbial antigens, this decrease may contribute to an altered response to microbial antigens in COPD airways .
There is substantial evidence suggesting increased DC concentrations in the lung parenchyma of patients with COPD [3-6], however, there are conflicting reports on blood DC concentrations in patients with COPD [21,34]. Galgani and colleagues postulated a decrease in blood pDCs (and a resulting increase in the mDC/pDC ratio) , whereas Kalathil and colleagues  and our study did not find differences in blood pDC concentrations between patients with COPD and controls. One possible explanation for the discrepancy between the studies might be differences in the medication of the patients, the severity of the disease and the presence of different comorbidities. Therefore, further studies are needed to better understand the regulation of pDC concentrations in COPD.
It has been postulated that mDCs can be subdivided into BDCA-1-positive mDCs (“mDC1”) and BDCA-3 positive mDCs (“mDC2”) [35,36], based on a study with blood mDCs from healthy volunteers . However, BDCA-3 can be upregulated on BDCA-1 positive mDCs . In human airways, both BDCA-1 and BDCA-3 are expressed on > 50% of all mDCs, suggesting an overlap in the expression of both markers [10,11,14]. In the current study, both markers were upregulated on blood mDCs (expression on > 60% of mDCs) in asymptomatic smokers and in patients with COPD suggesting that the clear distinction between these two blood mDC populations is lost in these conditions. The functional consequences of these findings are currently unclear and need further investigation.
This study shows, for the first time, that an imbalanced expression of co-stimulatory molecules on circulating DCs is associated with the severity of pulmonary emphysema in COPD. These findings will help to understand the immunopathogenesis of COPD.
Blood Dendritic Cell Antigen
C-C Chemokine Receptor 5
Cluster of Differentiation
Chronic Obstructive Pulmonary Disease
Fluorescence Activated Cell Sorter
- FEV1 :
Forced expiratory volume in the first second
Myeloid Dendritic Cell
Plasmacytoid Dendritic Cell
Programmed death ligand 1
Thymic stromal lymphopoietin
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We thank Petra Thamm for excellent technical assistance.
The authors declare that they have no competing interests.
PS, JCV and ML designed and supervised the study, analysed the data and wrote the manuscript draft; MU recruited and characterised the participants, obtained the blood samples and helped to perform the flow cytometric measurements; KB and KG planned and performed the flow cytometric measurements and analyses. All authors read and approved the final manuscript.
Antibodies used for flow cytometry. Figure S1. Gating of blood dendriticc cells. Figure S2. Histogram plots of mDC surface markers in blood. Figure S3. Histogram plots of pDC surface markers in blood. Figure S4. Markers of systemic inflammation in peripheral blood. Figure S5. Correlation of clinical parameters with Interleukin-6. Figure S6. Regulatory T cells (Tregs) in peripheral blood.