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. 2017 Dec 18;48(1):13–22. doi: 10.1111/cea.13061

Dendritic cell phenotype in severe asthma reflects clinical responsiveness to glucocorticoids

E S Chambers 1,3, A M Nanzer 1,2, P E Pfeffer 1,4, D F Richards 1, A R Martineau 2, C J Griffiths 2, C J Corrigan 1, C M Hawrylowicz 1,✉
PMCID: PMC5767735  PMID: 29130617

Summary

Background

Subsets of patients with severe asthma remain symptomatic despite prolonged, high‐dose glucocorticoid therapy. We hypothesized that the clinical glucocorticoid sensitivity of these asthmatics is reflected in differences in peripheral blood dendritic cell subsets.

Objective

To compare peripheral blood leucocyte populations using flow cytometry at baseline and after 2 weeks of systemic glucocorticoid (steroid) treatment to identify immunological differences between steroid‐sensitive (SS) and steroid‐resistant (SR) asthmatics.

Methods

Adult severe asthmatics (SS n = 12; SR n = 23) were assessed for their response to 2 weeks of therapy with oral prednisolone. Peripheral blood was obtained before and after therapy and stained for lymphocyte (CD3, CD19, CD4, CD8 and Foxp3) and dendritic cell markers (Lineage negative [CD3, CD14, CD16, CD19, CD20, CD56], HLA‐DR+, CD304, CD11c, ILT3 and CD86).

Results

A higher median frequency of myeloid DCs (mDCs) but not plasmacytoid DCs (pDCs) was observed in the blood of SR as compared to SS asthmatics (P = .03). Glucocorticoid therapy significantly increased median B cell, but not T cell numbers in both cohorts, with a trend for increased numbers of Foxp3+ Tregs in SS (P = .07), but not SR subjects. Oral prednisolone therapy significantly reduced the median numbers and frequencies of total DCs and pDCs in both SS and SR asthmatics. Interestingly, the expression of HLA‐DR and ILT3 was also reduced on pDCs in all patients. In contrast, therapy increased the median frequency of mDCs in SS, but reduced it in SR asthmatics.

Conclusions

Myeloid DC frequency is elevated in SR compared with SS asthmatics, and mDC shows a differential response to oral prednisolone therapy.

Keywords: asthma, dendritic cell, glucocorticoid, steroid resistant, steroid sensitive, T cells

1. INTRODUCTION

Asthma is characterized by airway hyperresponsiveness, T cell‐mediated inflammation, mucus hypersecretion and airway remodelling. Glucocorticoids (steroids) represent the cornerstone of contemporary asthma therapy, improving lung function and asthma symptoms in many patients (steroid sensitive, SS). Beyond these global features of asthma pathophysiology, however, evidence continues to accumulate about the heterogeneity of the disease in terms of its natural history, the nature and degree of associated airways inflammation and its responsiveness to steroid therapy.1 Indeed, it has been evident for some time that there exists a subgroup of asthmatic patients showing no demonstrable clinical benefit, at least in terms of short‐ to medium‐term improvement in lung function, in response to physiologically appropriate systemic steroid therapy (steroid resistant, SR). These patients are at risk of high morbidity and mortality, and as such pose an unmet clinical need.

Several mechanisms have been proposed to contribute to steroid non‐responsiveness at the cellular level, particularly in T cells, including overexpression of pro‐inflammatory transcriptional regulators such as NFκB and AP‐1, increased expression of histone deacetylases, polymorphisms of the IL‐10 gene, elevated expression of the dominant negative isoform of the glucocorticoid receptor GRβ, overexpression of Th2 cytokines and vitamin D insufficiency.2, 3, 4, 5, 6, 7, 8, 9, 10 More recent evidence also suggests that IL‐17A overexpression can be both a marker and a risk factor for severe and SR asthma.11, 12, 13, 14, 15, 16, 17

Notwithstanding these observations, there have been few if any studies of the dynamic effects of systemic glucocorticoid therapy in vivo, and in particular, whether glucocorticoids exert differential effects on lymphocyte frequency and functional differentiation in SS as compared with SR asthmatics, which may contribute to their different clinical responsiveness. Elucidating the mechanisms behind steroid‐resistant disease is vital to improving treatments for these patients. As asthmatic inflammation is postulated to be fundamentally lymphocyte driven, the cell types of particular interest, which may play a role in differential steroid responsiveness in SS and SR asthmatics, include lymphocytes such as CD4+ T cells including regulatory T cells (Tregs), CD8+ T cells, B cells and dendritic cells (DCs).8, 18 Dendritic cells are sentinels of the immune system, as they are early sensors of “stress” or pathogens, and when such signals are detected, they will mature and migrate to local lymph nodes to initiate an adaptive immune response. DCs present antigen‐derived peptides (such as those derived from processed allergens) bound to MHC molecules as well as costimulatory molecules (CD80 and CD86) to T cells which bind to the T cell receptor (TCR) and CD28, respectively, resulting in T cell activation and functional differentiation. In contrast inhibitory receptors, such as immunoglobulin‐like transcript 3 (ILT3), are associated with a more tolerogenic DC phenotype, as an expression of ILT3 has been shown to promote the generation of Foxp3+ Treg.19, 20, 21

There are 2 major subsets of DCs: myeloid dendritic cells (mDCs) and plasmacytoid dendritic cells (pDCs). The study of DCs is relevant to asthma as mDCs are resident in the airway mucosa and survey the airway lumen for antigen and particulates.22 Myeloid DCs have been shown to induce a Th2‐inflammatory response in the airways of asthmatics in response to aeroallergen exposure, which results in eosinophilic infiltration and disease exacerbation.23 Plasmacytoid DCs express high levels of IL‐3R, CD123, and MHC class II, and very low levels of costimulatory molecules, pDCs are specialized for production of high levels of anti‐viral type 1 interferon production and prime Th1 effector generation.24 However, pDCs may also play a role in generating tolerance to inhaled antigens,25 to protect the epithelium from damage caused by aberrant T cell responses to otherwise harmless antigens and particulates.

The aim of this study was to investigate differences in peripheral blood DC frequency, number and phenotype in clinically defined SS and SR asthma patients, and the impact of 2 weeks of oral prednisolone treatment on these parameters. We further investigated whether this was associated with any changes in lymphocyte frequency and numbers. We hypothesized that SS patients demonstrate a less activated, more tolerogenic DC phenotype in comparison with SR patients reflected in the frequency of their circulating, regulatory T cells, and that glucocorticoid treatment enhances this phenotype in SS individuals.

2. MATERIALS AND METHODS

2.1. Subjects

All patients recruited provided written, informed consent (National Research Ethics Committee 08/H0804/84). Eligible patients had a specialist physician diagnosis of moderate to severe asthma for at least 6 months and were managed with inhaled steroids and short‐ and long‐acting bronchodilators corresponding to therapy step 3 or 4 of the 2012 British Thoracic Society (BTS) guidelines on the management of asthma.26 At recruitment, all patients were required to demonstrate airways obstruction with a pre‐bronchodilator FEV1 of <80% of the predicted value, and clear reversibility of this obstruction in response to short‐acting bronchodilator (>12% improvement following inhalation of 400 μg of salbuterol). In addition, all patients had undergone a detailed assessment to exclude a diagnosis other than asthma and comorbidities affecting asthma control. Patients had not been exposed to systemic steroids for at least 4 weeks prior to the study. Patients on immunotherapy, smokers or patients who had symptoms and signs suggesting a respiratory tract infection or any asthma exacerbation during the 4 weeks prior to enrolment for the study were also excluded.

Eligible patients were characterized as steroid sensitive or resistant as defined by a ≥10% or <10% improvement, respectively, in baseline FEV1 following a pharmacodynamically standardized, a 14‐day course of oral prednisolone (40 mg/1.73 m2/d; Wockhardt UK Ltd, Wrexham, UK).27 Ongoing inhaled therapy was not altered during this treatment. Routine spirometry was measured before and after the course of prednisolone using a PC based spirometer and software (WinspiroPRO Medical International Research, Rome, Italy). Peripheral venous blood was obtained from all study subjects and collected into tubes containing sodium citrate and was directly stained as described below.

2.2. Flow cytometry

The following antibodies were used for ex vivo phenotyping of peripheral blood obtained from asthma donors: CD3, CD4, CD8, CD11c, CD14, CD16, CD19, CD20, CD56, CD86 and HLA‐DR (SK7, RPA‐T4, RPA‐T8, B‐ly6, MφP9, 3G8, HIB19, 2H7, NCAM16.2, 2331[FUN‐1] and L243, respectively; BD Biosciences, Oxford, UK), ILT3 and Foxp3 (ZM4.1 and PCH101, respectively; eBiosciences, Hatfield, UK) and CD304 (BDCA‐4) (AD5‐17F6; Miltenyi Biotec Bisley, UK). Red blood cells were lysed following staining with BD FACS lysing solution. Foxp3 staining was performed as previously described.18 Samples were subsequently processed on a FACSCalibur flow cytometer running CellQuest Pro software (BD Biosciences), which was also used for analysis. A live dead stain was not used as the flow cytometry staining was performed on whole blood ex vivo.

Absolute and differential blood leucocyte counts were performed routinely using a LH750 haematology analyser (Beckman Coulter, CA, USA) and analysed in conjunction with flow cytometric data to calculate cell numbers.

2.3. Cytometric bead array

Serum samples collected from the asthmatics were analysed for the following cytokines (IL‐1β, IL‐5, IL‐8, IL‐6, IL‐13, IL‐17A, IFNγ, GM‐CSF and TNFα) using a cytometric bead array according to the manufacturer's instructions (BD Bioscience). The lower limit of detection was 1.5 pg/mL.

2.4. Statistics

Data were assessed for equivalence to a Gaussian distribution and equality variance after which the appropriate parametric or nonparametric test was performed (see individual figure legends). Differences were considered significant at the 95% confidence level. Box‐and‐whisker plots represent the median, interquartile range and 10th to 90th percentiles, with outliers outside the 10th to 90th percentiles shown as individual points.

3. RESULTS

3.1. Study patients and clinical steroid responsiveness

Clinical and demographic details of the study patients have been published previously.28 Briefly, the asthmatic patients differentiated as steroid sensitive (SS) or SR based on their FEV1 response to a pharmacodynamically standardized course of oral prednisolone were otherwise well matched in terms of age, ethnicity, sex, atopic status, body mass index, total inhaled steroid dosage and baseline FEV1. Mean (95% CI) FEV1 significantly improved from 56.0 (47.4%‐64.6%) to 70.8 (62.6%‐79.0%) of the predicted value following prednisolone in the SS asthmatics (P < .0001), whereas in the SR patients there was no significant change: 61.3 (55.3%‐67.3%) to 59.7 (52.8%‐66.5%) (P = .18) (Table S1). Demographic data on healthy control subjects studied are also provided in Table S1.

3.2. Oral prednisolone significantly increases the number of peripheral blood B cells

Cell surface staining was performed on peripheral blood cells of severe asthmatics and healthy control subjects. No differences in the frequency of lymphocyte populations between healthy controls and the severe asthmatics were observed at baseline (Table 1).

Table 1.

The frequency of lymphocytes is similar between severe asthmatics and healthy controls

Healthy Severe asthma P value
CD19+ lymphocytes 7.32 (5.7‐8.9) 8.45 (7.2‐9.8) .37
CD3+ lymphocytes 59.70 (50.1‐69.3) 58.99 (55.1‐62.9) .87
CD4+ T cells 62.15 (55.3‐67.0) 65.10 (61.1‐69.06) .47
CD8+ T cells 29.91 (23.2‐36.7) 30.04 (26.2‐33.9) .97
CD3+/CD19+ ratio 8.96 (5.9‐12.0) 8.41 (7.1‐9.7) .70
Foxp3+ CD4+ T cells 7.99 (7.2‐8.8) 7.88 (6.9‐8.8) .46
n = 10 n = 35
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Healthy controls and severe asthmatics were assessed at baseline for lymphocyte populations including B Cells (CD19+), T cells (CD3+) and for T regulatory cells (Foxp3+CD4+ T cells). Data are shown as mean ± 5%‐95% confidence intervals.

Cell surface staining was also performed on SS and SR asthmatics before and after the 2‐week course of prednisolone, which was used to define their responder status. As previously reported,28 there were no significant differences between the groups in the median numbers of circulating total B cells, T cells, CD4+ T cells or CD8+ T cells prior to oral prednisolone treatment. Following treatment with oral prednisolone, no significant change in the median total numbers of circulating lymphocytes in the SR and SS asthmatic was seen (Figure 1A). The median total numbers of circulating B cells, as defined by CD19+ cell surface expression, significantly increased in both groups post‐prednisolone without significant change in the median total numbers of circulating T cells (as defined by CD3+ cell surface expression), CD4+ T cells or CD8+ T cells (Figure 1B). Prednisolone therapy was also associated with a trend towards an increase in the median total number of circulating Foxp3+ T regulatory cells in the SS, but not the SR asthmatics (Figure 1C). This staining was performed ex vivo on whole blood to ascertain that we were looking at “real” Treg populations, as it has been reported that Foxp3 can be induced in T effector cells by activation. Therefore, in a number of severe asthmatics, we included in the staining protocol antibodies specific for CD25 and CD127, as cells that are CD25high and CD127low are reported to represent Treg cells with suppressive function.29 The Foxp3+ CD4+ T cells that we identified as Tregs had >90% of cells falling in the gate CD25hiCD127lo, whereas the Foxp3‐ T cells had only 2.9% of cells falling in the gate (Figure S1A). Also, when the frequency of CD4+ Foxp3+ cells was correlated with the frequency of CD127loCD25hi T cells, there was a significant positive correlation between these 2 populations (r = .752 P < .0001) strongly suggesting that we are looking at “true” Treg cells (Figure S1B). The MFI of Foxp3 in the Foxp3+ Treg cells is also shown, although no difference was observed between the 2 groups (Figure S1C).

Figure 1.

Figure 1

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Absolute lymphocyte counts in the peripheral blood of steroid‐sensitive (SS) and steroid‐resistant (SR) severe asthmatics before (pre‐) and after (post‐) a 2‐week course of oral prednisolone. A, total lymphocytes; B, total B cells (CD19+), T cells (CD3+), CD4+ and CD8+ T cells; C, total Foxp3+ CD4+ T cells; D, eosinophil to the neutrophil ratio in the peripheral blood of SS and SR severe asthmatics. Data assessed by Wilcoxon matched‐pairs test *P < .05, **P < .01, ****P < .001

No difference in the eosinophil and neutrophil numbers was previously reported between SS and SR asthmatics pre‐steroids.28 Here we show that there is a significant reduction in the ratio of eosinophils to neutrophils in both SS and SR asthmatics after prednisolone treatment (Figure 1D).

3.3. Increased frequency of myeloid dendritic cells in the peripheral blood of steroid‐resistant as compared to steroid‐sensitive asthmatics

Dendritic cells (DCs) are sentinels of the immune system; DCs were characterized as being lineage cocktail (CD3, CD14, CD16, CD19, CD20 and CD56) negative and HLA‐DR+ cells. Two major DC subsets, myeloid and plasmacytoid (mDC and pDC, respectively), can be distinguished based on cell surface expression of 2 well‐characterized molecules CD11c for mDCs and CD304 (BDCA‐4; Neuropilin 1) for pDCs30 (Figure 2A). The median frequency of CD11c+ mDCs, within the Lineage‐HLA‐DR+ gate, was significantly elevated in the peripheral blood of the SR as compared to the SS asthmatics, whereas there was no significant difference in the median frequencies of CD304 pDCs between the 2 patient groups (Figure 2B). This resulted in a trend (P = .09) towards an increased ratio of mDC:pDC cells in the SR as compared to the SS asthmatics (Figure 2C).

Figure 2.

Figure 2

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Increased frequency of mDCs in the peripheral blood of steroid‐resistant (SR) as compared to steroid‐sensitive (SS) severe asthmatics. A, example gating of dendritic cell (DC) gating: DCs were identified as being lineage cocktail negative (CD3, CD14, CD16, CD19, CD20 and CD56) and HLA‐DR+ and then subsequently either CD11c+ (mDCs) or CD304+ (pDCs); B, cumulative data of frequency of mDCs and pDCs; and C, the ratio of CD11c+ as compared to BDCA‐4+ DCs in the peripheral blood of SS and SR severe asthmatics prior to any glucocorticoid treatment. Data assessed by Mann‐Whitney U statistical test *P < .05

We also measured cell surface expression of HLA‐DR and the costimulatory molecule CD86 on mDCs and pDCs, as well as that of the Immunoglobulin‐like transcript 3 (ILT3), an inhibitory receptor implicated in promoting tolerance in T cells.19, 20, 21 Myeloid DCs expressed significantly higher surface CD86 and HLA‐DR, as measured by median fluorescence intensity, but lower surface ILT3 as compared to pDCs (Figure 3A; P < .001 in each case). We observed no significant difference, however, in the median intensity of expression of these cell surface molecules in the SS vs SR asthmatic patients (Figure 3B).

Figure 3.

Figure 3

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Expression of surface CD86, ILT3 and HLA‐DR on myeloid (mDCs) and plasmacytoid (pDCs) dendritic cells in the peripheral blood of steroid‐sensitive (SS) and steroid‐resistant (SR) asthmatics. Expression of costimulatory and inhibitory receptors on DCs was assessed by flow cytometric analysis in SS and SR patients at baseline prior to glucocorticoid treatment. A, example histograms of CD86 (top), ILT3 (middle) and HLA‐DR (bottom) expression on mDCs (blue) and pDCs (red) and fluorescence minus one (FMO) control (grey shaded); B, cumulative data on mDCs (white) and pDCs (grey) in the peripheral blood of SS and SR severe asthmatics. Data assessed by paired t test **P < .01, ***P < .001, ****P < .0001

3.4. Prednisolone treatment significantly decreased total dendritic cells and plasmacytoid dendritic cells frequencies

As shown in Figure 4, a 2‐week course of oral prednisolone resulted in a significant reduction in the median frequencies of total DCs in the leucocyte population of both SS and SR asthmatics (Figure 4A). This was reflected in a reduction in the median absolute number of total DCs in SR asthmatics (P < .01), but not in SS asthmatics (P = .23; Figure 4B). There was a significant reduction in the median absolute number and frequency of pDCs in both SS and SR asthmatics. In contrast, quite different effects of prednisolone were observed on mDCs in the two severe asthma groups. In the SR asthmatics, there was a significant reduction in the median frequency and number of peripheral blood mDCs following prednisolone therapy. Conversely, in the SS asthmatics, there was a significant increase in the median frequency (P < .05), which is most likely due to the decreased frequency of pDCs in the Lineage‐HLA‐DR+ gate. This is reflected in the lack of change in the median absolute number (P = .77) of mDCs following prednisolone therapy (Figure 4A and B). Interestingly, these changes in DC subtypes resulted in a significant increase (P < .001) in the median overall ratio of mDCs to pDCs in the SS, but not the SR patients (Figure 4C).

Figure 4.

Figure 4

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Reduced frequencies and numbers of dendritic cells (DC)s in the peripheral blood of asthmatics following prednisolone therapy. Steroid‐sensitive (SS) and steroid‐resistant (SR) asthmatics were assessed before and after a 2‐week course of oral prednisolone therapy (A) frequencies and (B) total numbers of total DCs, mDCs and pDCs; (C) the ratio of CD11c+ as compared to CD304+ DCs in the peripheral blood of steroid‐sensitive (SS; white) and steroid‐resistant (SR; grey) severe asthmatics before and after 2 weeks of prednisolone therapy. Data assessed by Mann‐Whitney U test *P < .05, **P < .01, ***P < .001

The expression of surface CD86, HLA‐DR and ILT3 was also measured on peripheral blood mDCs and pDCs from the SS and SR asthmatics before and after prednisolone therapy (Table 2). Steroid therapy was associated with reduced expression of ILT3 and HLA‐DR on pDCs in both the SS and SR asthmatics, whereas there was no significant effect on CD86 expression. There was no significant effect of steroids on the ILT3 expression on mDCs. There was, however, a suggestion of a differential effect of prednisolone on mDC cell surface expression of CD86 and HLA‐DR in the SS, as compared with the SR asthmatic patients: there was a trend towards reduced expression of CD86 (P = .088) and HLA‐DR (P = .065) on mDCs in the SS patients which was not observed in the SR patients (Table 2).

Table 2.

Expression of immunoglobulin‐like transcript 3 (ILT3) and costimulatory molecules on dendritic cells (DC)s before and after corticosteroid therapy

Steroid sensitive P value Steroid refractory P value
Pre‐steroids Post‐steroids Pre‐steroids Post‐steroids
pDCs
ILT3 expression 63.44 (48.56‐78.32) 43.64 (32.3‐55.0) .028 60.33 (48.8‐71.87) 31.89 (26.4‐37.4) <.0001
CD86 expression 21.59 (9.9‐33.31) 19.55 (3.2‐35.9) .693 14.13 (10.5‐17.7) 17.74 (11.6‐23.7) .251
HLA‐DR expression 105.0 (82.3‐127.7) 76.03 (51.2‐100.8) .012 112.2 (89.7‐134.7) 80.28 (62.6‐97.9) .032
mDCs
ILT3 expression 27.82 (21.0‐34.6) 26.38 (22.0‐30.8) .700 27.24 (21.4‐33.1) 26.37 (22.0‐30.8) .781
CD86 expression 63.19 (50.1‐76.3) 51.29 (38.8‐63.8) .088 57.72 (41.9‐98.7) 52.82 (41.9‐67.4) .258
HLA‐DR expression 170.1 (130.4‐209.9) 129.2 (98.9‐159.4) .065 161.6 (107.1‐216.1) 132.2 (111.3‐153.0) .262
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Mean fluorescence intensity (MFI) of cell surface expression of CD86, HLA‐DR and inhibitory receptor ILT3 on pDCs (CD304+; top) and mDCs (CD11c+, bottom) before and after 2 weeks of prednisolone therapy. Data are shown as mean ± 5%‐95% confidence intervals.

3.5. Steroid treatment does not significantly alter the serum cytokine profile

Steroids are known to alter cytokine secretion by multiple cell types, and these cytokines in turn can regulate lymphocyte and dendritic cell populations. The concentration of a number of cytokines in the serum of healthy and severe asthmatics (pre‐ and post‐steroids) was therefore investigated to explore whether these might reflect and/or contribute to the differences observed in the frequency of Tregs and DCs in the peripheral blood. A range of cytokines was assessed; however, the cytokines IL‐1β, IL‐5, IL‐21, IFNγ and GM‐CSF were undetectable in the majority of samples assessed. Interestingly, the healthy control subjects had significantly higher IL‐13 in their serum as compared to the severe asthmatics (P = .0002), whilst conversely, asthma patients had higher levels of IL‐6 and IL‐8 as compared to the healthy controls (both P < .0001; Figure 5A). However, there was no significant difference in the quantities of cytokines in the serum of SS and SR asthmatics at baseline. Treatment of SR asthmatics with prednisolone resulted in a significant reduction in the cytokines IL‐6, IL‐8 and IL‐23p40, which was not observed in the SS; however, this may be due to the lower number of SS individuals (Figure 5B). These differences, whilst of interest, do not obviously explain the differences observed in the DC and Treg populations reported here.

Figure 5.

Figure 5

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A reduction in serum IL‐6, IL‐8 and IL‐23p40 in SR asthmatics after prednisolone treatment. Serum cytokine concentrations were assessed by cytometric bead array in (A) healthy controls (white) and severe asthmatics (grey) and (B) steroid‐sensitive (SS; white) and steroid‐resistant (SR; black) asthmatics pre‐ and post‐prednisolone treatment. Data assessed by Wilcoxon matched‐pairs test *P < .05, **P < .01, ***P < .001, ****P < .0001

4. DISCUSSION

The present study sought to determine whether differences could be detected in circulating leucocyte populations between disease severity‐matched SS and SR asthma patients. Our findings support our original hypothesis that SS patients demonstrate a less activated DC phenotype and that glucocorticoid treatment enhances this phenotype in SS individuals in comparison with SR patients. Specifically, we observed that a significantly higher frequency of mDCs was present in the peripheral blood of SR as compared to SS asthmatics at baseline. Although prednisolone treatment resulted in an increased frequency of circulating mDC in the SS cohort, these cells demonstrated a trend towards a less stimulatory phenotype with reduced expression of HLA‐DR and CD86, as well as a trend for an increase in the circulating Foxp3+ Treg population, which contrasted with our observations in the SR cohort. Thus, we demonstrate that significant differences resided within the mDC compartment, both at baseline and following 2 weeks of oral prednisolone therapy, which appears to reflect a more activated immune phenotype in SR as compared to SS patients. Importantly, both the SS and SR received the same regimen of oral prednisolone (14‐day course of oral prednisolone at 40 mg/1.73 m2/d), and there was no difference in the inhaled mean equivalent inhaled glucocorticoid dosages taken by both groups (P = .60) as shown previously28; therefore, the differences observed here are likely due to the 2‐week course of prednisolone.

Several of the outcomes examined in this study revealed no differences between SS and SR patients, or confirmed independent observations in different disease cohorts. For example, the frequencies of B cells and T cells in the peripheral blood of SS compared with SR severe asthmatics were comparable at baseline. A significant increase in the frequencies and total numbers of B cells was observed in both the SS and SR asthmatics following oral steroids which, as far as we are aware, has not been previously observed in patients with asthma. However, an earlier study observed a similar change in patients with multiple sclerosis post‐methylprednisolone treatment.31 Although of significant interest, as these changes occurred in both SS and SR populations, they may not be indicative of important mechanisms underlying the clinical benefit of steroids in asthma. These data are in contrast to a recent publication which showed that that there was an increase in the numbers of B and T cells in the peripheral blood 24 hours after oral steroids which reverted to baseline within 7 days,32 although in that study a different steroid regimen was employed as compared to our study, and a day 14 time‐point was not addressed.

A major observation arising from the current study is that a significantly higher frequency of mDCs was present in the peripheral blood of SR as compared to SS asthmatics at baseline, resulting in an increase in the ratio of mDCs/pDCs. There was also a trend for mDCs to exhibit higher expression of CD86 and HLA‐DR, but lower expression of the inhibitory receptor ILT3 than pDCs. These data suggest, along with earlier independent studies, that mDCs are better able to initiate immune responses due to their higher expression of HLA‐DR and CD86.33 Thus, the ratio of mDCs to pDCs may have important implications in the context of allergic and asthmatic disease. Models of allergic airway disease suggest that whilst both mDCs and pDCs take up allergen, the pDC population may preferentially induce tolerance to an inhaled allergen.25, 34 Additionally, pDCs play an important role in combating respiratory infections (a common trigger of asthma exacerbations), and in children, the number of peripheral pDCs has been reported to be inversely correlated with symptoms of lower respiratory infections,35 so changes in the ratio of mDC:pDC could impact asthma exacerbations.

Myeloid DCs have been shown to initiate Th2‐mediated disease leading to eosinophilic lung inflammation in mice.23 Recently two independent studies have also proposed that a subset of murine mDCs (CD11b+) play a vital role in the induction of Th17 responses in the mucosal tissue by secreting Th17‐polarizing molecules such as IL‐23p19, IL‐6 and TGF‐β.36, 37 These data may be of relevance to steroid refractory asthma, as IL‐17A expression is elevated in both the airways and cultured peripheral blood of more severe asthmatics, implicating IL‐17A in steroid‐resistant disease.11, 13, 14, 15, 16, 17 Asthmatics have enhanced effector responses associated with disease, and this may plausibly result from an increased frequency and/or stimulatory capacity of their mDCs; additionally, asthmatics have been demonstrated to have lower numbers of Foxp3+ Tregs.38, 39, 40 Our earlier study reported reduced circulating Foxp3+ T cells in SR compared to SS individuals.18 Here we report a trend towards an increase in the circulating Foxp3+ Treg population following oral steroid therapy in SS patients, which supports and extends earlier independent work showing increased Foxp3 expression and numbers of Foxp3+ cells following systemic steroid therapy of moderate/mild asthmatics or patients with immune thrombocytopenic purpura.41, 42 Notably this was not observed in SR asthmatics, suggesting that failure to enhance the frequency of Treg cells by steroids may be a factor contributing to clinical resistance, although further studies are warranted to strengthen this observation. These would include, in addition to studying a greater number of subjects, the inclusion of additional markers to define Tregs (such as CTLA‐4, LAP, GARP or LAG3) and assays of suppressive function. Nevertheless, these data are also consistent with the hypothesis that therapies that increase or maintain the Foxp3+ Treg population, such as vitamin D, provide greater therapeutic benefit.18, 43, 44

An unexpected, but interesting observation from this study is that for certain immune parameters, the response of SR asthmatics to prednisolone treatment is similar to that of SS asthmatics, such as the reduction in the number of B cells, and pDCs, whilst others clearly show a different pattern of regulation by prednisolone. This includes the effects on Tregs and on mDCs discussed further below, as well as the reduction in the serum inflammatory cytokine production in the SR but not in the SS. Thus, we conclude that steroid resistance appears to be associated with a differential response to steroids at the immunological level rather than no response.

In the present study, 2 weeks of prednisolone treatment caused a significant reduction in the frequency of total DCs, as well as pDCs, in the peripheral blood of severe asthmatics. This corresponds with other studies in patients suffering from autoimmune disease where intravenous methylprednisolone treatment caused a reduction in the frequency of plasmacytoid DCs in the peripheral blood.25, 31, 45 This is proposed to reflect the susceptibility of pDCs to glucocorticoid‐induced apoptosis,46 although additional effects of steroids on DC homing cannot be ruled out.

The most notable differential response to oral prednisolone treatment in SS and SR patients was observed at the level of mDCs. There was a significant increase in the frequency of circulating mDCs in SS asthmatics following steroid therapy alongside a trend for decreased CD86 and HLA‐DR expression on these cells, likely to render the SS mDCs less stimulatory. The reduction in the expression of CD86 and HLA‐DR is presumed to occur as a direct consequence of the prednisolone treatment on the mDCs, as has been shown previously in vitro.47 Notably, this change in the frequency of SS mDCs post‐steroids was not reflected in a change in the overall number, and this may therefore largely reflect the profound inhibition of pDCs post‐prednisolone. Although there was a significant fall in the median frequency and number of mDCs in the peripheral blood of SR asthmatics following steroid therapy, there was no significant effect on costimulatory molecule expression, so the cells are likely to remain highly stimulatory. We can only speculate as to the reasons for the differential effects of oral prednisolone treatment on mDC populations in SS vs SR asthma patients: it is likely to include a complex outcome of the effects of steroids on the numbers of mDCs produced in bone marrow, those recruited into lymph nodes and tissues and potentially also cell survival.48 Whether, and how, each of these steps is differentially regulated in SS vs SR asthma is, as far as we are aware, not clearly delineated and represents an important area for future research, beyond the scope of the present study. A limitation of the current study is that the data are from the peripheral blood only. A recent study reported differences in myeloid DC in the sputum of children with steroid‐treated asthma as compared to age‐matched healthy children, although differences pre‐ and post‐steroid treatment were not reported.49 To gain a full insight into what is happening in our patients, it would have been informative to have studied bronchoalveolar lavage (BAL) samples in parallel with peripheral blood from the same individual, pre‐ and post‐prednisolone treatment. However, bronchoscopy with BAL carries risks and side effects, especially in severe asthmatics, and was not therefore part of the current study design.

Another limitation of the current study is the paucity of DC markers that were utilized, and with hindsight, it would have been informative to have included, at the very least, the markers CD1c and CD141 to further differentiate mDC subpopulations into conventional type 1 (cDC1s) and conventional type 2 (cDC2s).50, 51, 52 Very recent studies highlight more extensive panels of antigens that can be used to further dissect mDc populations.53 Thus, it would have been informative to have investigated whether, and how, prednisolone targeted these different type of mDC populations.

Collectively, these data demonstrate the differential effects of 2 weeks of oral prednisolone therapy on circulating leucocyte populations as well as the contrasting effects of this therapy on SS and SR severe asthmatics with novel differences seen in mDCs between the 2 types of severe asthmatic. We believe the data from this study warrant further investigations in severe asthma as to whether the differential effects of oral prednisolone on mDCs, as well as Foxp3+ Tregs, have a translational impact as a biomarker of clinical responsiveness to steroids.

CONFLICT OF INTEREST

The authors declare no conflict of interest.

Supporting information

 

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ACKNOWLEDGEMENTS

ESC was funded by a MRC British Thoracic Society/Morriston Davies Trust Capacity Building PhD Studentship and subsequently funded by an MRC Centenary Fellowship. AMN was funded by Asthma UK. PEP held a Wellcome Trust Clinical Research Training Fellowship. The research was funded/supported by the National Institute for Health Research (NIHR) Biomedical Research Centre based at Guy's and St Thomas’ NHS Foundation Trust and King's College London. The views expressed are those of the authors and not necessarily those of the NHS, the NIHR or the Department of Health.

Chambers ES, Nanzer AM, Pfeffer PE, et al. Dendritic cell phenotype in severe asthma reflects clinical responsiveness to glucocorticoids. Clin Exp Allergy. 2018;48:13–22. https://doi.org/10.1111/cea.13061

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