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Central European Journal of Immunology
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2/2013
vol. 38
 
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Clinical immunology
The metabolic activity of neutrophils measured with a chemiluminescence assay in young patients with type 1 diabetes depending on the disease duration

Magdalena Kaczmarek
,
Zdzisława Iwanicka
,
Adam Jankowski
,
Aleksandra Lewandowicz-Uszyńska

(Centr Eur J Immunol 2013; 38 (2): 237-242)
Online publish date: 2013/07/08
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Introduction

Many pathologies result from physical and chemical reactions that lead to the formation of highly reactive forms of oxygen referred to as free radicals [1, 2]. They originate mainly from processes occurring inside granulocytes which activate the NADPH oxidase enzyme system, which produces a phenomenon called a respiratory burst [3]. Released RT are necessary for intracellular destruction of many microorganisms, acting with granulocyte enzymes as an essential part of the immune system that protects against most pathogens. RT released into the extracellular space or as a result of excessive activation of neutrophils, or due to a decreased activity of enzymes neutralizing their activity (SOD, catalase, peroxidase), or as a result of lipid peroxidation, lead to the formation of protein oxidation products, and damage the surrounding cells and even tissues, leading to the development of inflammation and autoimmune processes [4-7]. Diabetes is one of the conditions in which the processes leading to the damage of pancreatic islet  cells are closely related to the free radical pathology [8-11]. Elevated blood glucose increases oxidative stress and release of free radicals, thereby causing the activation of NF-kB [12]. It is believed that excessive activation of neutrophils may occur a few or more months ahead of the onset of symptoms, and the then produced RT along with a network of pro-inflammatory cytokines, nitric oxide, and autoreactive T cells may in favourable conditions (genetic background, infections, stress, dietary errors) lead to the destruction of the islets of Langerhans [13-17].

Therefore, the aim of this study was to assess the metabolic activity of neutrophils in children with type 1 diabetes, depending on the disease duration, compared to the control group.

Material and methods

The study involved 87 children with type 1 diabetes aged 4 to 21 years (52 girls and 35 boys, mean age 13 years) who were patients of the Clinic of Developmental Endocrinology, Wroclaw Medical University (in 2000/2001). Depending on the disease duration, patients were divided into four subgroups:

• subgroup I – the disease duration up to 12 months (35 children),

• subgroup II – the disease duration up to 5 years (28 children),

• subgroup III – the disease duration up to 10 years (12 children),

• subgroup IV – the disease duration over 10 years (12 children).

The control group consisted of 23 people – healthy volunteers aged 20 to 25 years (mean age 23 years).

All patients were receiving humanized insulin injections several times a day from the early onset of diabetes mellitus. The study was approved by the Bioethics Committee (858/01-03) at the Wroclaw Medical University.

The material for this study was venous blood collected during basic diagnostic tests or checks into plastic tubes with heparin in a closed system. The metabolic activity of neutrophils was measured using a luminol-dependent chemiluminescence assay. The spontaneous and stimulated neutrophil CL was studied (fMLP, opsonised Zymosan, PMA) in a 96-well white microplate (LB96P-WMP) according to Lewkowicz et al. [18]. The order of addition and volume of reagents are shown below:

No stimulation: FMLP :

1. PBS 40 l 1. PBS 20 l

2. Luminol 20 l 2. fMLP 20 l

3. Whole blood 40 l 3. Luminol 20 l

4. Whole blood 40 l

PMA: Zymosan:

1. PBS 20 l 1. PBS 20 l

2. PMA 20 l 2. Zymosan 20 l

3. Luminol 20 l 3. Luminol 20 l

4. Whole blood 40 l 4. Whole blood 40 l



Each of the systems was repeated three times, and the arithmetic mean of the values received was calculated. The study was conducted using a chemiluminescence luminometer (LB 96P MicroLumat of E&G Barthold). The device was controlled by WinGlow software in the Windows environment. Spot measurements were taken within 0.2 seconds every 60 seconds at 37°C. The test took 45 minutes. Results are expressed in RLU (Relative Light Units/s) as the maximum chemiluminescence (CLmax). Since CL depends linearly on the number of neutrophils, while heme compounds reduce its value, the chemiluminescence results were adjusted to their absolute number and haemoglobin content in the blood tested by the formula:

Hb [%]

CLCALCULATED = CLDETERMINED × ––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––––

PMN [%] × WBC [thous./100 µl]



where Hb is haemoglobin and PMN is the percentage of neutrophils in the total number of white blood cells (WBC).

A statistical analysis conducted using the Mann-Whitney U test involved determination of the arithmetic mean, standard deviation, and the level of significance (p < 0.05) for each parameter of neutrophil CL in examined patients and the control group. Using the Kruskal-Wallis ANOVA by Ranks test, box and whisker plots were made showing individual parameters of neutrophil CL including the mean, standard deviation and standard error for examined patients and the control group.

Results

The results of spontaneous neutrophil CL are summarized in Fig. 1. Significantly lower CL values were shown in all children with diabetes, regardless of the disease duration. There were no statistically significant differences in spontaneous neutrophil CL values between subgroups I and II, II and III, III and IV, I and III, I and IV. Significantly lower values of spontaneous CL were observed in subgroup IV in comparison with the results obtained in subgroup II. The effect of fMLP stimulation of neutrophils in the examined group is presented in Fig. 2. Significantly lower values of neutrophil CL were demonstrated in subgroups I, III and IV, compared to the control group. There were no statistically significant differences between the CLmax levels in subgroup II, compared to healthy subjects. The lowest values of CL after stimulation with fMLP were found in subgroup III, i.e. in children with diabetes in the time interval from 5 to 10 years. There were no statistically significant differences in CLmax levels between subgroups I and II, II and III, III and IV, and between I and III, I and IV, II and IV. Neutrophil response to stimulation with PMA is given in Fig. 3. All subgroups of children with diabetes had significantly lower CLmax values, compared to the control group. The weakest response to PMA stimulation was observed in subgroup III (i.e. in children in whom the disease lasts from 5 to 10 years). There were no statistically significant differences in the maximum values of neutrophil CL between subgroups I and II, I and IV, and II and IV. Figure 4 presents CLmax results after stimulation with opsonised Zymosan. Significantly lower neutrophil CL was reported in all the examined subgroups, compared to the control group. The lowest levels of neutrophil CL were observed in children with newly detected diabetes. There were statistically significant differences in CLmax between subgroups I and II, and I and IV. There were no statistically significant differences in the values of Zymosan-activated neutrophil CL between subgroups II and III, III and IV, as well as I and III, II and IV.

Discussion

Maintaining the stability of the neutrophils-RT-antioxidant enzymes system determines maintaining RT concentrations at the appropriate level that is sufficient to protect against infectious agents, without causing damage associated with excessive proliferation of these compounds. Telci et al. [19] showed elevated levels of markers of oxidative damage to proteins and decreased plasma antioxidant capacity in children with type 1 diabetes, compared to the control group. Studies showing impaired neutrophil oxidative metabolism in patients with diabetes were conducted as early as in the 1990s [20, 21]. Decreased oxidative metabolism of neutrophils measured with a chemiluminescence assay was also demonstrated in children with type 1 diabetes in a variety of clinical conditions (good, medium, severe), compared to healthy subjects [22]. In the present study, all tested systems (spontaneous and stimulated CL) showed impaired neutrophil oxidative metabolism in all subgroups of children with diabetes, compared with the control group. Thus, impaired response of neutrophils to both receptor stimulation (fMLP, Zymosan) and non-receptor stimulation (PMA) was reported. A similar observation was made by Nishizawa et al. [23] who showed impaired neutrophil CL after stimulation with fMLP in patients with type 1 diabetes, compared to healthy subjects. Kantara et al. [24] reported significantly enhanced spontaneous CL in patients with diabetes compared to healthy subjects, which was not observed in the present study. PMA stimulation of neutrophils resulted in convergent observation, i.e. a significant reduction in CL in comparison with healthy subjects. It is worth noting that the lowest CL values were found in children from subgroup III (after stimulation with fMLP and PMA). In subgroup IV, i.e. in children with the longest disease duration (over 10 years) CL results (after stimulation with PMA) were statistically significantly higher than in children from subgroup III. Longer duration of diabetes increases the risk of the so-called late complications (microangiopathy, vascular lesions) directly related to RT activity [25]. Perhaps the slight increase of CL observed in children with the longest disease duration indicates the beginning of the process. It is noteworthy that the lowest CL levels (after stimulation with Zymosan) were reported in children with newly detected diabetes. This may indicate that neutrophil dysfunctions (related to the processes of phagocytosis and CL) occur at an early stage of the disease. Descamps et al. [26] showed no changes in spontaneous neutrophil CL in patients with newly detected diabetes (the tests were performed 2 months after the onset of diabetes). After stimulation with fMLP and PMA, the researchers observed enhanced neutrophil CL. After three months of treatment, CL reached the normal values of healthy subjects. Unfortunately, the research was not continued in a longer time interval. The fact of poor response to this type of neutrophil stimulation explains the tendency of patients with suspected or newly detected diabetes to have frequent infections during this period. In the present study, the situation observed in children with diabetes was similar to that of recurrent respiratory infections in children and adults [27-29], in which a decline in neutrophil CL, probably resulting from recurrent infections, was observed. Perhaps chronic activation leads to the depletion of neutrophil energy reserves and consequently to a decline in their CL. The possibility of the existence of different functional states of neutrophils, including the state of “exhaustion”, has been described by various authors [30]. In this study chronic pre-activation of neutrophils in a high concentration of glucose in the body can decrease the sensitivity of these cells to subsequent stimuli. The reduced neutrophil CL in children with type 1 diabetes observed in this study is in apparent contradiction to the fact of excessive activity of neutrophils in the pathophysiology of diabetes. It must be noted that the oxidative burst of neutrophils is influenced by various factors, such as certain drugs, impaired glucose profile, insulin, blood ph disorders associated with the accumulation of acidic metabolites, and finally elevated levels of haemoglobin and its derivatives which significantly reduce neutrophil CL in whole blood [31, 32]. The presence of elevated levels of glycated haemoglobin (HbA1C) in erythrocytes in patients with uncontrolled diabetes may be the essence of this phenomenon. Studies conducted in vitro by Oldenborg et al. [31] on healthy people showed inhibition of neutrophil chemiluminescence after stimulation with fMLP by insulin. Gallacher et al. [34] found lower CL values in adults with diabetes, compared to the control group. The authors also found a negative correlation between blood levels of chemiluminescence and HbA1C. Thus, the weakening of neutrophil bactericidal function should be associated not only with direct changes in blood glucose levels, but also with poor metabolic control of the disease. Another cause of impaired neutrophil oxidative metabolism may be the response of these cells to insulin. Saeed et al. [27] showed impaired neutrophil oxidative metabolism using a CL array in patients with diabetes, and they attributed the inhibitory role to acidic metabolites (acetoacetate) present in the serum of these patients. Delamaire et al. [36] also showed impaired neutrophil oxidative metabolism (chemotaxis, chemiluminescence) in patients with type 1 diabetes. Just as in the present study, the PMA and Zymosan-stimulated CL of neutrophils was lower, compared to healthy subjects. Marhoffer et al. [37] demonstrated lower neutrophil CL after stimulation with PMA in diabetic patients, compared to healthy individuals. Assessing the phenomena associated with RT generation, we should, if possible, include processes occurring inside neutrophils as well as processes associated with the so-called extracellular CL resulting from lipid peroxidation of cell membranes (directly independent of NADPH oxidase), however, as a consequence leading to tissue damage and the accumulation of metabolites (malonic aldehyde) associated with the activity of other free radicals and nitric oxide [38].

Conclusions

Children with diabetes, regardless of the disease duration, had impaired spontaneous oxidative metabolism of neutrophils measured with a chemiluminescence assay in comparison to the control group.



The authors declare no conflict of interest.

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Copyright: © 2013 Polish Society of Experimental and Clinical Immunology 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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