- Research article
- Open Access
- Open Peer Review
Interleukin-4 and 13 concentrations in infants at risk to develop Bronchopulmonary Dysplasia
© Baier et al; licensee BioMed Central Ltd. 2003
- Received: 28 March 2003
- Accepted: 18 August 2003
- Published: 18 August 2003
An exaggerated inflammatory response occurs in the first few days of life in infants who subsequently develop bronchopulmonary dysplasia (BPD). The increase of inflammatory cytokines in many disease processes is generally balanced by a rise in anti-inflammatory cytokines. Interleukin-4 (IL-4) and interleukin-13 (IL-13) have been shown to inhibit production of several inflammatory cytokines important in the development of BPD.
We sought to determine if a correlation exists between the presence or absence of IL-4 and IL-13 in tracheal aspirates (TA) during the first 3 weeks of life and the development of BPD in premature infants. Serial TAs were prospectively obtained from 36 very low birth weight infants and IL-4 and IL-13 concentrations were determined by ELISA.
Infants who developed BPD (n = 19) were less mature (25.3 ± 0.02 wks vs. 27.8 ± 0.05 wks; p < 0.001), and had lower birth weights (739 ± 27 g vs.1052 ± 41 g; p < 0.001). IL-4 and IL-13 were detectable in only 27 of 132 and 9 of 132 samples assayed respectively. Furthermore, the levels detected for IL-4 and IL-13 were very low and did not correlate with the development of BPD.
TA concentrations of IL-4 and IL-13 do not increase significantly during acute lung injury in premature infants.
- Premature Infant
- Acute Lung Injury
- Neonatal Intensive Care Unit
- Bronchopulmonary Dysplasia
- Tracheal Aspirate
An exaggerated inflammatory response occurs in the first few days of life in infants who subsequently develop bronchopulmonary dysplasia (BPD). This response includes an increase in airway protein, inflammatory cells and cytokines [1–7]. Increased concentrations of inflammatory cytokines such as interleukin-1β (IL-1β), interleukin-6 (IL-6), macrophage inflammatory protein 1α (MIP-1α), tumor necrosis factor-α (TNFα) and interleukin-8 (IL-8) have been found in the tracheal aspirates (TA) of infants who developed BPD [3–8]. Additionally, the magnitude of the inflammatory response seems to correlate with the infant's ability to recover fully from acute lung injury that occurs with hyaline membrane disease.
Inflammatory responses may be modulated by several anti-inflammatory or otherwise immunomodulatory cytokines. The role of these cytokines in the pulmonary inflammatory response of the preterm newborn with hyaline membrane disease or its progression to BPD has had little study. Interleukin-10, which inhibits cytokine production from activated macrophages, is undetectable or present only at very low concentrations in the TAs from preterm infants during the first 3 days of life . These observations suggest an absence of immunomodulatory cytokines, particularly those that down regulate inflammation in the premature infant's lung, may play a role in the development of BPD.
Interleukin-4 (IL-4) and interleukin-13 (IL-13) are structurally related cytokines that share similar properties and receptor components . The actions of these cytokines are pleiotropic, some may be beneficial in moderating lung inflammation, and others may be detrimental. For example, IL-4 and IL-13 have both been shown to inhibit production of several inflammatory cytokines that may be important in the development of BPD in vivo and in vitro [11–18]. However, increased IL-4 and IL-13 expression and production is associated with the development of bronchial hyperreactivity and asthma, which are significant long term complications of BPD [19, 20].
Since information on the possible role of IL-4 and IL-13 in the pathogenesis of BPD is unknown, we designed a study to determine the role of these cytokines in the development of BPD. Specifically, we prospectively determined tracheal aspirate concentrations of IL-4 and IL-13 during the first 3 weeks of life in mechanically ventilated very low birth weight infants who did and did not develop BPD. Our goal was to determine if a correlation exists between the presence or absence of these cytokines in tracheal aspirates and the development of BPD in premature infants.
The study population consisted of very low birth weight infants admitted to the neonatal intensive care unit (NICU) at the Louisiana State University Health Sciences Center in Shreveport. Patients were admitted to the NICU between February 1997 and March 1998. Eligibility criteria included: a birth weight of less than 1500 grams, mechanical ventilation (MV) during the first day of life, and informed consent. Infants who were not expected to survive for 24 hours and those with major respiratory, cardiovascular or neurological anomalies were excluded. The study was approved by the Institutional Review Board for Human Research at LSUHSC.
Tracheal aspirates were collected when clinically indicated. Sterile normal saline (0.5 ml) was instilled into the endotracheal tube and 3–4 manual breaths were provided using a self inflating bag. Airway secretions were aspirated into sterile traps and any material remaining in the catheter was washed into the trap with an additional 0.5 cc saline. Serial aspirates were obtained at 0–24 hours, 48–72 hours, 4–5 days, 7–9 days, 12–14 days and on day 21 if the infant remained on mechanical ventilation. Routine bacterial and genital mycoplasma cultures were performed on tracheal aspirates collected in the first 24 hours. All TAs were frozen at -20°C until assayed for cytokines by enzyme linked immunoassay (ELISA).
Clinical management of the infants was directed by the attending neonatologists. The use and timing of steroids and indomethacin prophylaxis were not specified by the protocol. Demographic data collected in this study included; the need for surfactant therapy, duration of MV, use of corticosteroids, incidence of patent ductus arteriosus (PDA), use of indomethacin (prophylactic and therapeutic), presence and severity of intraventricular hemorrhage (IVH), and the presence of periventricular leukomalacia (PVL). Maternal data included mode of delivery, complications of pregnancy, the use of antenatal steroids and antibiotics.
Several definitions of BPD have been used through the years. Initially BPD was defined as oxygen dependency at 28 days of age [21, 22]. More recently, the use of oxygen dependency at 36 weeks PCA has been proposed as a more suitable definition of BPD . Both of these definitions however, predict long term respiratory abnormalities . More recently a NIH consensus has proposed new definitions and diagnostic criteria that provide gradation of BPD into mild, moderate and severe forms . Since even mild BPD may presage chronic respiratory problems we used the earlier broader definition of BPD (defined as oxygen dependency at 28 days postnatal age and a chest radiograph showing changes compatible with BPD) [24, 21].
The recombinant human cytokines IL-4 and IL-13, monoclonal and biotinylated monoclonal antibodies to IL-4 and IL-13 were purchased from Endogen (Woburn, MA). Streptavidin-horseradish peroxidase (Strep-HRP) conjugate was purchased from Pharmingen (San Diego, CA). Poly horseradish peroxidase-streptavidin (PolyHRP-Strep) and dilution buffer were obtained from Endogen. Horseradish peroxidase-conjugated rabbit anti-goat antibody, monoclonal and polyclonal goat anti-human secretory component antibodies, bovine serum albumin (BSA), and oxalic acid were purchased from Sigma Chemical Co (St. Louis, MO). Human secretory IgA was purchased from ICN Pharmaceuticals (Costa Mesa, CA). ELISA plates were obtained from Costar (Cambridge, MA). 2,2'-azino-di [3-ethyl-benzthiazoline-6-sulphonic acid] (ATBS) and 3, 3', 5, 5'-tetramethylbenzidine (TMB) peroxidase substrate kits were purchased from Bio-RAD (Hercules, CA).
Concentrations of coating and detecting antibodies were titrated to optimize assay conditions. The ELISAs were validated in TAs by adding 1000 pg of recombinant cytokine to a pooled sample of TA with low or undetectable concentrations and comparing measured cytokine concentrations with what was added. Recovery was >80% of added cytokines. The R-squared values of the standard curves for these assays were generally greater than 0.95 with most assays having R-squared value of 0.99. Assays with standard curves with R-squared values less than 0.9 were repeated.
ELISA plates for IL-4 and IL-13 assays were coated with 100 μl of the appropriate monoclonal antibody in PBS (pH 7.4) overnight at 4°C. The coating antibodies were used at the following concentrations: IL-4, 3.4 μg/ml; IL-13, 3.8 μg/ml; and secretory component, 2.0 μg/ml. After coating, the ELISA plates were washed 3 times (5 minutes per wash) with 200 μl of phosphate buffered saline (PBS) containing 0.05% Tween 20 (wash buffer). All subsequent washes were performed similarly. The plates were then blocked using 200 μl PBS – Tween 20 containing 3% (w/v) BSA (blocking buffer) overnight at 4°C. After blocking, the plates were washed 3 times in wash buffer prior to use. All subsequent steps were performed in blocking buffer. Tracheal aspirates and recombinant cytokine standards were diluted in blocking buffer.
For the IL-4 ELISA, 50 μl TA (diluted 1:1 in blocking buffer) or recombinant cytokine standards (7.8–1000 pg/ml) were incubated in antibody coated ELISA plates for 1 hour at room temperature. Without washing or removing standards/samples (in accordance to manufacturers specifications), 50 μl biotinylated monoclonal anti-IL-4 antibody (500 ng/ml) was added and incubated for another 1 hour at room temperature. The plates were washed 4 times and then incubated with Strep-HRP (1:1000) for 30 minutes at room temperature. After washing 4 times, 100 ul TMB substrate was added to develop color. The reaction was stopped by adding 100 μl of 0.2 N sulphuric acid and the plates were read at 450 nm.
For the IL-13 ELISA, 50 μl TA (diluted 1:1 in blocking buffer) or recombinant cytokine standards (3.9–1000 pg/ml) were incubated in antibody coated ELISA plates for 1 hour at room temperature. Without washing or removing standards/samples, 50 μl biotinylated monoclonal anti-IL-13 antibody (500 ng/ml) was added and incubated for another 1 hour at room temperature. The plates were washed 4 times and then incubated with polyHRP-streptavidin conjugate (1:7000 in dilution buffer) for 30 minutes at room temperature. After washing 4 times, the plates were developed as described above.
The ELISAs for secretory component has been previously described . TA samples were diluted 1:400 to 1:6400 (in blocking buffer) for the secretory component assay.
Sensitivities of the assays were as follows: IL-4, 15 pg/ml; IL-13, 3.9 pg/ml; secretory component; 3 ng/ml.
To adjust for variation in collection of tracheal aspirates, cytokine concentrations were normalized to secretory component . Statistical analysis was performed using the SPSS for Windows version 6.0 (SPSS Inc., Chicago, IL). Chi square analysis was used to assess the statistical differences in categorical variables. The Student t-test was used to assess normally distributed variables. The duration of mechanical ventilation, oxygen use and hospitalization were not normally distributed therefore; the Wilcoxon Rank Sum test was used for analysis of these factors. The differences in TA cytokine concentrations were assessed using ANOVA. Differences in IL-4 concentrations between infants with and without BPD at each time point were also assessed post hoc using Wilcoxon Rank Sum test (data not normally distributed) without correction. A probability value of less than 0.05 was considered statistically significant. The data are presented as mean ± standard error of the mean (SEM).
Clinical characteristics of Study Subjects
BPD n = 19
no BPD n = 17
Birth weight (grams)
739 ± 27
1052 ± 42
25.3 ± 0.2
27.8 ± 0.5
42 ± 13
7 ± 2
64 ± 12
11 ± 2
104 ± 12
69 ± 6
MV > 28 days
Supplemental O2 at 36 weeks PCA
Age steroids started (days)
8 ± 2
9 ± 2
Inflammation is the primary pathological process that precedes the development of BPD. Increased tracheal concentrations of inflammatory cytokines have been reported in infants who develop this disease [3–8]. Interleukin-4 and IL-13 have been shown to modulate lung inflammation in animal models and thus the presence or absence of these cytokines in the lung may be important determinants in the pathogenesis of BPD [16, 28].
Interleukin-4 is a pleiotropic cytokine produced predominately by T-lymphocytes and alveolar macrophages [10, 29]. Interleukin-4 stimulates production of some cytokines and growth factors while inhibiting others [11–17, 30]. Although IL-4 may be inhibitory to some aspects of lung inflammation, the presence of IL-4 may be detrimental by inducing proliferation of, and collagen production by, subsets of lung fibroblasts [31, 32]. Further, IL-4 is a central mediator in the development of asthma . We detected very low concentrations of IL-4 in only one fifth of the tracheal aspirates. This suggests that IL-4 does not play a major role in the lung injury, or protection from lung injury, associated with BPD. The role of IL-4 later in the course of the disease was not assessed in this study.
Interleukin-13, which is similar in structure and function to IL-4, is produced by activated TH2 lymphocytes and alveolar macrophages [10, 33]. Interleukin-13 inhibits inflammatory cytokine production in macrophages and epithelial cells and upregulates the anti-inflammatory cytokine, interleukin-1 receptor antagonist . Thus, IL-13 potentially moderates lung inflammation. In adult fibrotic lung diseases significantly increased concentrations of IL-13 can be detected in bronchoalveolar lavage (BAL) fluid suggesting an up-regulation of this cytokine in response to lung inflammation . As with IL-4, it has been shown in animal models that IL-13 protects against inflammatory lung injury . In contrast, IL-13 was rarely detected in tracheal aspirates of premature infants with acute lung injury, and when detected, was well below physiologic concentrations required for biologic activity. These observations suggest that very premature neonates may be unable to produce physiologic concentrations of this cytokine in the lung. This suggests that proinflammatory processes in the lungs of the premature infant may be relatively unchecked compared to the adult. Thus, as with IL-4, IL-13 does not appear to have a role in modulating pulmonary inflammatory responses in preterm infants at risk of developing BPD.
The mechanisms responsible for the inability of premature infants to increase concentrations of IL-4 or IL-13 in response to a significant lung inflammation are unclear. It could be that the cells that produce these cytokines are not present in the airways and lungs of the premature newborn. Alveolar macrophages, one of the cells types that produce IL-4 are not usually present in the lung at birth in the absence of congential pneumonia but populate the lungs shortly after birth. An influx mononuclear cells and macrophages are part of the inflammatory response that presages BPD . Thus, it seems likely that the right cell types are present in the lung after birth. This suggests that the ability to produce IL-4 or IL-13 in the lung may be developmentally regulated. Therefore, a functionally immature lung may lack the ability to produce these down regulators of inflammation. This may in part explain the exaggerated inflammatory response frequently observed in infants who develop BPD. Consistent with this hypothesis is the report that cord blood mononuclear cells do not produce significant IL-4 in response to endotoxin . Further, we were not able to demonstrate IL-13 production by lipopolysaccharide (LPS) stimulated cord blood cells (unpublished observations).
The role of airway colonization with Uu in the development of chronic lung disease is unclear. Most, but not all studies, suggest that isolation of Uu from tracheal aspirates is associated with an increased incidence of chronic lung disease in very low birth weight infants [35–37]. The frequency of Uu isolation in our infants and the increased incidence of BPD is in agreement with other reports [35–37].
Postnatal steroids were used frequently in this study. At the time when these infants were cared for in our NICU, it was our practice to treat infants who were ventilator dependent for more than 7 days with systemic dexamethasone. Corticosteroid administration (either antenatal or postnatal) could potentially inhibit IL-4 production . We did not observe an effect of antenatal or postnatal steroids on IL-4 concentrations. The lack of effect of postnatal steroids on IL-4 may be due to the time (on average 8 postnatal days) when these were started. At that time IL-4 concentrations were declining.
All studies of this nature suffer from limitations inherent in their design. Tracheal aspirate cytokine concentrations may not reflect what is happening at the alveolus or interstitium of the lung. In addition, values of IL-4 or IL-13 normalized to secretory component do not directly estimate the concentration of these compounds in the epithelial lining fluid (ELF) of the lung. In a few samples the raw concentration of IL-4 was greater than 100 pg/ml. This is within the range of biological activity of IL-4. IL-4 concentrations as low as 10 pg/ml have been reported to cause partial inhibition of LPS induced IL-8 production in peripheral blood monocytes in vitro. Thus, it is possible that biologically significant concentrations of these cytokines are present in some infants with developing BPD.
This study examined a relatively small number of tracheal aspirates in a small number of infants. This sample size which was sufficient to detect large differences in cytokine production between BPD and control infants is not sufficiently powered to detect smaller differences . Thus it is possible that smaller magnitude differences in IL-4 (and IL-13) do exist between control and BPD infants and would have been detected with a larger sample. The clinical importance of these small magnitude differences is uncertain. Additionally, most patients had mild-moderate BPD and there were few patients who developed severe BPD. These infants (severe BPD) could have different patterns in IL-4 or IL-13 production that are not obvious in our study.
In clinical practice infants are extubated as soon as feasible to limit potential damage from continuing ventilation. Therefore, infants who have less severe lung disease or recover from their acute lung injury rapidly are not sampled. Thus, there are disproportionately fewer samples and fewer time points in infants who recover or do not develop chronic lung disease. This may introduce bias into our results limiting the conclusions that may be drawn. However, we believe that our results are consistent with other similar clinical studies and in animal models of lung injury providing further insight into the mechanisms of chronic lung injury in the newborn.
In summary we have shown that TA concentrations of IL-4 and IL-13 do not increase significantly during acute lung injury in premature infants. Further studies are required to determine the role (if any) of these and other anti-inflammatory mediators in the pathogenesis of chronic lung disease.
The authors would like to thank the nurses and respiratory therapists in the NICU who helped with specimen collection.
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