Open Access

The cytokine interleukin-26 as a biomarker in pediatric asthma

  • Jon R. Konradsen1, 2, 3,
  • Björn Nordlund2, 3, 4,
  • Bettina Levänen5,
  • Gunilla Hedlin2, 3, 4 and
  • Anders Linden5, 6Email author
Respiratory Research201617:32

https://doi.org/10.1186/s12931-016-0351-6

Received: 9 January 2016

Accepted: 23 March 2016

Published: 31 March 2016

Abstract

In this pilot study, we examined associations between local interleukin (IL)-26, disease severity and biomarkers of Th2-mediated inflammation in a well-defined cohort of pediatric patients (14 years median age, 41 % females) with controlled (n = 28) or uncontrolled (n = 48) asthma. Sputum IL-26 protein concentrations (ELISA) reflected disease control in patients without local (low exhaled nitric oxide) or systemic (low blood eosinophils) signs of eosinophilic inflammation. Moreover, sputum-IL-26 concentrations correlated with those of blood neutrophils. Our study indicates that IL-26 is a potential biomarker of disease severity in pediatric asthma without signs of Th2-mediated inflammation.

Keywords

Asthma Children Eosinophil FENO IL-26 Neutrophil Sputum

Introduction

Dear Editor,

Up to 20 % of children with severe asthma have no signs of eosinophilic inflammation [1] and these pediatric patients respond poorly to inhaled corticosteroids and anti-IgE, pharmacotherapy that was originally designed to target severe Th2-mediated inflammation [2]. For these patients, there is a need to increase the understanding of the immunological events underlying the disease, to establish biomarkers for improved diagnosis and monitoring, as well as to identify potential targets for therapy [2].

The presumed Th17 cytokine interleukin (IL)-26 is an intriguing member of the IL-10 family; one that is involved in several chronic inflammatory disorders and can exert both pro- and anti-inflammatory actions, depending upon the setting [3]. However, there is currently no conclusive information on the involvement of IL-26 in the pathogenesis of asthma or any other chronic inflammatory airway disorder [4]. A recent study on healthy human subjects indicates that this cytokine is produced by Th17 cells, as well as by other leukocytes, and that IL-26 contributes to the mobilization of neutrophils in the airways during activation of pulmonary host defense by endotoxin [5]. Given these facts, we hypothesized that local IL-26 is associated with severe disease in pediatric asthma lacking signs of eosinophilic inflammation.

Methods

To address our hypothesis, we utilized data from a previously well-characterized cohort of school-age children (n = 76) with severe uncontrolled (uncontrolled) or persistent controlled (controlled) asthma [6]. Briefly, uncontrolled asthma was diagnosed in a child with reduced asthma control despite treatment with high doses of inhaled corticosteroids (≥800 μg budesonide equivalent per 24 h), whereas controlled asthma was defined as children having an acceptable asthma control with a low to moderate daily dose of inhaled corticosteroids (100–400 μg budesonide equivalent per 24 h). The patients were recruited as previously described [6], after approval by the Regional Ethics Review Committee in Stockholm (Stockholm) and after informed consent from each patient or parent, in full accordance with the Helsinki declaration.

We quantified IL-26 protein concentrations in the airways in relation to asthma severity, blood eosinophils (B-EOS), exhaled nitric oxide (FENO) and blood neutrophils (B-NEUTRO). Specifically, we utilized cell-free samples of induced sputum [7] for the measurement of IL-26 protein concentrations (ng/mL) with ELISA (Cusabio Biotech®) [5].

Results

Among our included pediatric patients, the median age (range) was 13.7 years (7–19), with 41 % being females. The 48 patients with uncontrolled asthma had a reduced score on the asthma control test (17 versus 23, p < 0.001), and a lower FEV1 (82 % versus 90 % predicted, p = 0.04) despite receiving a higher dose of inhaled corticosteroids (800 μg versus 320 μg of budesonide, p < 0.001) compared to the 28 children with controlled asthma. In addition, the children with uncontrolled asthma had higher concentrations of B-EOS (0.4 versus 0.2, p = 0.02) and B-NEUTRO (3.2 versus. 2.6, p = 0.03) than those with controlled asthma.

In the entire cohort, the median FENO levels were 18.3 p.p.b and the median B-EOS concentration was 0.3×109/L. These median values were used to categorize children into groups with high and low levels of these biomarkers of Th2-mediated inflammation, independently of the predefined severity classification.

Among children with low concentrations B-EOS (≤0.3*109/L), we observed higher concentrations of IL-26 in uncontrolled compared to controlled asthma (Fig. 1a & Table 1). Furthermore, we found a corresponding association between asthma control and IL-26 concentrations among children with low levels of FENO (Fig. 1b & Table 1). A trend towards an association between asthma control and IL-26 concentrations in the entire cohort was observed, but it was not statistically significant (Table 1). Furthermore, when investigating children with high concentrations of B-EOS and high levels of FENO, the difference in distribution of IL-26 between children with uncontrolled and controlled asthma was less pronounced (Table 1).
Fig. 1

Median concentrations (logarithmically transformed) of IL-26 (ng/mL) in induced sputum from children with uncontrolled versus controlled asthma and a low concentrations of eosinophils in blood (≤0.3 × 109/L) or b low levels of exhaled nitric oxide (≤ 18.3 p.p.b)

Table 1

Interleukin-26 in the airways of children with uncontrolled versus controlled asthma

 

IL-26 (ng/ml) Uncontrolled asthma

n

IL-26 (ng/ml) Controlled asthma

n

p-value*

All patients

4.4 (1.9–14)

48

2.4 (1.3–4.5)

28

0.077

Low B-EOS (≤ 0.3×109/L)

4.6 (2.3–13)

27

2.3 (1.3–4.5)

22

0.038*

High B-EOS (>0.3×109/L)

4.1 (1.7–16)

21

2.9 (1–31)

5

0.61

Low FENO (≤18.3 p.p.b.)

4.1 (2.2–16)

23

2.0 (1.2–3.6)

13

0.055

High FENO (>18.3 p.p.b)

5.0 (1.8–13)

25

2.7 (1.4–24)

15

0.54

Footnotes. The IL-26 concentrations are presented as medians with inter-quartile ranges

The median values in the entire cohort of the respective biomarker were used to define the cut-off between high and low levels of the various biomarkers. B-EOS blood eosinophils, FENO the fraction of nitric oxide in exhaled air, in parts per billion. *Independent samples, analyzed by Mann–Whitney U-test (SPSS® version 20)

Finally, we found a weak but statistically significant correlation (the Pearson test: r = 0.27, p = 0.018, n = 76) between the concentrations of B-NEUTRO and IL-26 in the entire cohort of pediatric patients with asthma and this correlation tended to be stronger in the patients with low levels of FENO (r = 0.35, p = 0.036, n = 36). There was no evident correlation between IL-26 concentrations and age, gender, height or dose of inhaled corticosteroids.

Discussion

Our study is the first to associate local IL-26 protein concentrations in the airways with a certain clinical phenotype of pediatric asthma. The fact that IL-26 protein concentrations are increased in sputum from pediatric patients with uncontrolled asthma but without signs of Th2-mediated inflammation forwards IL-26 as a potential, novel biomarker of disease severity in this phenotype of asthma. These findings are also supported by a positive correlation between local IL-26 and systemic neutrophils (ie. B-NEUTRO); a correlation in line with a mechanistic link between IL-26 and the mobilization of neutrophils as recently indicated in human airways [5, 8].

One of the effects of treatment with inhaled corticosteroid is an inhibition of the production of Th2 cytokines such as IL-4 and IL-5, which subsequently attenuate eosinophilic recruitment and the release of toxic granulae proteins [9]. The observed clinical effects are an improvement of symptoms and pulmonary function and a reduced rate of asthma exacerbations [10]. It is widely accepted that increased concentrations of blood eosinophils and high levels of FENO indicate systemic and local eosinophilic inflammation, respectively [11, 12]. In addition, it is known that low levels of these established biomarkers are associated with a reduced sensitivity to inhaled steroids [13, 14]. Given that our findings are compatible with an increase in local IL-26 being associated with inflammation not mediated by Th2-related mechanisms; this observation forwards the clinically relevant question whether IL-26 is also linked to low sensitivity to inhaled steroids in pediatric patients with non-allergic asthma? New studies are required to address this possibility; a possibility that has implications for the estimated 13 % of children with severe asthma displaying excess neutrophil mobilization [1].

Even though the size of our study material was modest, a particular strength of our current analysis is the standardized and detailed characterization of each individual patient; making it possible to identify various subgroups within this cohort. We think that this facilitated the discovery that IL-26 provides a potentially clinically relevant signal in patients without signs of local or systemic eosinophilic inflammation.

Conclusion

Our pilot study demonstrates that local IL-26 bears potential as a biomarker of disease severity in a clinical phenotype of pediatric asthma that is perpetuated by other than Th2-related mechanisms.

Abbreviations

B-EOS: 

blood eosinophils

B-NEUTRO: 

blood neutrophils

FENO: 

the fraction of nitric oxide in exhaled air

FEV1

forced expiratory volume during 1 s

IL: 

interleukin

Th: 

T helper

Declarations

Acknowledgements

For statistical considerations, Max Vikström, Ph.D., Unit for Cardiovascular Epidemiology, Institute of Environmental Medicine, Karolinska Institutet, was consulted. Funding for this study was obtained from the Centre for Allergy Research at Karolinska Institutet, the Freemason Child House Foundation in Stockholm, the Konsul Th. C. Bergh’s Foundation, the Swedish Asthma and Allergy Association’s Research Foundation, the Pediatric Research Foundation of Astrid Lindgren Children’s Hospital, and the Swedish Heart-Lung Foundation.

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Authors’ Affiliations

(1)
Clinical Immunology and Allergy Unit, Department of Medicine Solna, Karolinska Institutet and Karolinska University Hospital
(2)
Centre for Allergy Research, Karolinska Institutet
(3)
Astrid Lindgren Children’s Hospital, Karolinska University Hospital Solna
(4)
Department of Women’s and Children’s Health, Karolinska Institutet
(5)
Unit for Lung and Airway Research, Institute of Environmental Medicine, Karolinska Institutet
(6)
Lung Allergy Clinic, Karolinska University Hospital Solna

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Copyright

© Konradsen et al. 2016

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