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Medical Studies/Studia Medyczne
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Original paper

Assessment of concentrations of interleukin-25 in bronchial asthma – preliminary studies

Małgorzata A. Czarny-Działak, Anna Słuszniak

Medical Studies/Studia Medyczne 2016; 32 (4): 269–273
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Introduction

Asthma is a chronic inflammatory disease of the airways, which affects between 1% and 18% of people depending on the country (there are countries where prevalence is high, such as England or New Zealand, and those in which it is low, such as Albania and Greece) [1]. Most therapeutic problems are related to the so-called “difficult to treat asthma” – it is now believed that up to 10% of patients with asthma do not respond to standard treatment [2]. It is these patients who are saddled with the highest risk of death, and it is for them that there is a need to concentrate on trials of innovative diagnostic and treatment [3]. Allergic asthma is a chronic respiratory disease, which is inflammatory, and in which many cells and released by the substance – in this process a major role is played by cytokines from Th2 cells [1]. A major role is also played in inflammation in asthma by mast cells, released mediators of which cause bronchospasm and eosinophils, also via the release of eosinophil major basic protein (EMBP), which damages the lining of the airways [2]. the diagnostic process should therefore be concentrated on the treatment of these cells and of the released by substances. Individual cytokines have a very diverse role in the development or suppression of allergic inflammation. Cytokines are molecules of a glycoprotein, and they regulate many vital functions of cells. They are involved in inflammatory reactions and in the regulation of immune and haematopoietic processes [4–7]. Frequently they have a pleiotropic mechanism of action (the ability to act on various cells and induce various effects) and redundancy (when different cytokines produce the same effect). They may also act in relation to each other synergistically or antagonistically and induce a cascade feedback, positive and negative. Cytokines exert their action only by the presence of specific target cells for these receptors. They usually carry information between cells in very small distances [5].
Interleukin (IL)-25 belongs to the IL-17 cytokine family, which also shows pleiotropic properties; its receptor is IL-17RB receptor [8]. Its former name was IL-17E. To the IL-17 family, besides IL-17E, also belong: IL-176, IL17-C, IL-170, and IL-17F – each of them is characterised by certain differences in action [5]. Interleukin 25 is excreted by helper lymphocytes Th2 and mast cells, it inhibits production of IL-1 and IL-23 [9, 10], whereas it induces production of other cytokines, such as IL-4, IL-5, IL-13, and eotaxin in different tissues, mainly by Th2 lymphocytes, acting in an autocrine and paracrine way [11]. It stimulates eosinophils and production of IgE antibodies related to development of allergy. It is stated that IL-25 improves regulatory surface of adhesion molecule – ICAM-1 and inhibits the other molecule – ICAM-3 provides selection of eosinophils depending on the amount of the interleukin – IL-25. Due to this, IL-25 facilitates the leukocyte extravasation (diapedesis) processes of neutrophils, which are important factors in the development of the severe form of asthma. It has been proven that after applying antibody directed against the adhesion molecule (ICAM-1), the inflow of neutrophils to the respiratory tract is lessened. Interleukin 25 also extends the lifespan of eosinophils, the major cells in the inflammatory process in asthma [12]. Interleukin takes part in chronic inflammation, especially in the gastrointestinal tract, and induces inflammation in the lungs and respiratory tracts [13]. It is known that it is the cytokine which controls type 2 immune response, and especially important is its role in controlling the initiation and the severity of Th2 response course that is done via other cytokines: IL-4, IL-5, and IL-13. As we know, the Th2 advantage over Th1 is characteristic for allergic diseases [13]. It has a dual mechanism of action. On the one hand, it is a cytokine that prevents debilitating inflammation – suppressing development of chronic inflammatory diseases; on the other hand, it boosts immune response, thus fostering development of inflammatory diseases such as asthma or other allergic diseases. The action of IL-25 is well known in the case of animal models, whereas its mechanism of action in the case of humans requires further research [12]. Knowledge of the mechanism of action of IL-25 may be relevant to a new therapeutic approach in the treatment of asthma.

Aim of the research

The aim of the study was to assess whether levels of IL-25 in bronchial asthma depend on the degree of its gravity.

Material and methods

The blood samples were taken (from ulnar veins) from a group of 80 respondents (20 volunteers and 60 patients suffering from asthma: 20 with chronic mild asthma, 20 with moderate, and 20 with severe) into tubes with gel – with no anticoagulant, which were left for 30 min at room temperature. Next, after the end of the coagulation process, the samples were swirled for 20 min at 2500 rpm (1000 × g). Then serum was separated into 3 tubes, and samples were stored at –70°C until collection of the appropriate number of respondents. Concentration of interleukin was determined by enzyme-linked immunosorbent assay ELISA, with the use of reagent kit SEB 694 Hu. The actual measuring range of the kit varied from 15.6 to 1000 ng/ml. After the initial dilution of the standard 10,000 pg/ml, standards 1000 pg/ml, 500 pg/ml, 250 pg/ml, 125 pg/ml, 62.5 pg/ml, 31.2 pg/ml, and 15.6 pg/ml were obtained. In the kit 96-well plates coated with IL-25-specific antibodies conjugated with biotin were utilised. After adding standards and patients’ serum, the well plates were incubated for 2 h at 37°C. Content was extracted and 100 µl of reagent A added. Next, the well plates were incubated for 1 h at 37°C. After triple rinsing of wells, 100 µl of reagent B was added and incubated for another 30 min at 37°C. Content was extracted; the well plates rinsed five times. 90 µl of substrate solution (TMB) was added and the well plates were incubated for 20 min at 37°C (protecting them from direct sunlight).
Next, 50 µl of sulphuric acid (stop solution) was added in order to complete the reaction.
The well plates were read at 450 nm on an ELISA reader with the possibility of automatic calculation of concentration. The concentration of IL-25 in samples was determined by comparing the optical density of the sample, compared to the standard curve. In 17 of 80 test samples, a colour reaction was observed; however, it was not as significant as differentiation between the blind test and the lowest calibration point on the calibration curve (15.6 pg/ml).
According to the observations, concentration of IL-25 in the group of patients were in the lower range of the calibration curve. In order to adjust the calibration curve to the tested group of patients, during subsequent set, a variant without 1000 pg/ml and 500 pg/ml standards should be considered (these calibration points are rejected by the reader as the optical density is located over the measurement capabilities of the reader) as well as expanding incubation time, after adding TMB, to 25 min (the producer gives an alloying time of reaction of 15–25 min). We will assume that the extension of reaction time to maximum will enable us to measure lower concentrations, which – in a standard procedure – were not differentiated (they were located below the lowest standard). In the study 80 people participated: 20 volunteers and 60 patients suffering from asthma: 20 with chronic mild asthma, 20 with moderate, and 20 with severe. The grouping criteria to a certain degree of severity were clinical signs, categorised according to the Global Initiative for Asthma (GINA) (Tables 1 and 2).
Among patients were 18 men and 42 women, patients’ age ranged from 19 to 82 years. In the group of patients suffering from severe asthma, there were 7 men and 13 women; among patients with chronic moderate asthma there were 6 men and 14 women; and among patients with mild asthma there were also 6 men and 14 women. Affiliation to a given group was assessed by the degree of severity that was included in GINA consensus. Among the tested group, in 6 cases autoimmune aggression diseases were diagnosed: 2 patients with mild asthma, 2 moderate, and 2 severe. All patients were treated at the Healthy Lungs Clinic.
Blood for analysis of IL-25 was sampled from every patient, using the ELISA method.
Spirometry was done to all the patients (during medical examinations at the clinic). The inclusion criterion was diagnosed chronic asthma during the disease control period. Exclusion criteria were age below 18 and over 85 years, as well as loss of control over the disease. Volunteers did not suffer from any chronic illnesses, including allergic diseases. Laboratory tests were carried out at Świętokrzyskie Oncology Centre in the Institute of Cancer Markers. We received permission from the Bioethics Committee to carry out the tests.

Results

Among all respondents no elevated level of IL-25 was identified, whereas among 17 of the respondents higher concentrations of IL-25 were identified. Among them were 4 volunteers (20%) and 13 patients suffering from with asthma, including 6 suffering from chronic severe asthma (30%), 4 (20%) – moderate, 3 (15%) – mild. Among them, 3 patients had coexisting systemic disease (2 – severe asthma, 1 – mild asthma). A colour reaction was observed in 17 cases; however, it was not as significant as differentiation between the blind test and the lowest calibration point at the calibration curve (Tables 3 and 4).
Among volunteers who were identified with higher IL-25 levels compared to other respondents, one fact is worth considering: all the respondents had infection of the respiratory tracts just after the test. All of them had positive familial history of allergic disease. However, the respondents were free from any chronic diseases (Table 5).

Discussion

Research which has been published to date suggests that IL-25 can activate eosinophils during allergic dermatitis [14] and is one of the key cytokines which take part in Th2 response in asthma [13, 15]. This interleukin takes part in the induction of inflammation in respiratory tracts. It is known that asthma is a chronic inflammatory disease of the respiratory tracts [12, 16]. Especially vital is that action of the IL-25cytokine in controlling the initiation and severity of the course of Th2 response is done via other cytokines: IL-4, IL-5, and IL-13. This leads to dominance of Th2 response. It is known that the dominance of Th2 over Th1 is characteristic of allergic diseases [13]. It facilitates the process of penetration of neutrophils through the walls of blood vessels into inflamed tissues. The neutrophils are significant factors in the development of severe asthma. The above data suggest that the concentration of interleukin should increase along with the increase of the severity of the disease. However, its mechanism of action is well known in the case of the laboratory animals, but it requires further research in the case of humans [12]. In the study no precise answer was given. However, it should be noted that despite the lack of clear results, respondents among whom higher concentration of IL-25 interleukin was identified [17] suffered from severe asthma [6] or moderate asthma [4]; among them were also volunteers [4]. However, they all had positive familial history of allergic diseases. The fact that these volunteers had some features of infections after the research is not negligible. It is possible that during the test they had subclinical inflammation. The obtained results may, to some extent, suggest that the more severe the course of asthma, the higher the concentration of IL-25; however, the results are preliminary. We truly hope that further research will help to obtain more precise data because asthma is associated with enormous socioeconomic costs [1]. The most costly treatment – multi-drug regime – concerns severe asthma, especially so-called difficult-to-treat asthma [2, 17–19]. It seems that application of a single therapeutic means (e.g. antibody) not only reduce costs but also facilitates treatment of individual patients and, in some cases, enables maintaining control over the disease. This is why the IL-25 test seems to be crucial.

Conclusions

Perhaps the lack of elevated levels of IL-25 in serum in all patients was due the fact that these were people with controlled asthma. In the future patients should be checked during exacerbations of asthma and have it tried the response time to the maximum so that we can measure lower concentrations, which within a standard procedure have not been varied (found below the lowest standard). Therefore, we take our survey as preliminary to further understanding the action of this cytokine in patients with bronchial asthma.

Conflict of interest

The authors declare no conflict of interest.

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Address for correspondence:

Małgorzata A. Czarny-Działak MD, PhD
Department of Family Medicine and Geriatrics
Institute of Medical Sciences
Faculty of Medicine and Health Science
Jan Kochanowski University
ul. Malachitowa 32A, 25-705 Kielce, Poland
Phone: +48 602 570 179
E-mail: drmczarny@interia.pl
Copyright: © 2016 Jan Kochanowski University in Kielce This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License (http://creativecommons.org/licenses/by-nc-sa/4.0/), allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
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