Impact of IL8 and IL8-Receptor alpha polymorphisms on the genetics of bronchial asthma and severe RSV infections
© Puthothu et al; licensee BioMed Central Ltd. 2006
Received: 27 December 2005
Accepted: 17 February 2006
Published: 17 February 2006
Interleukin 8 (IL8) belongs to the family of chemokines. It mediates the activation and migration of neutrophils from peripheral blood into tissue and hereby plays a pivotal role in the initiation of inflammation. Thus it is important in inflammatory lung diseases like bronchial asthma or severe infections by Respiratory Syncytial Virus (RSV). IL8 acts through binding to the IL8-Receptor alpha (IL8RA). For both genes association with asthma has been described. In addition, IL8 has been found in association with RSV bronchiolitis. The aim of our study was to test both genes for association with asthma and severe RSV infections. In addition we were interested in whether a common genetic background of both diseases exists in regards to these genes.
We genotyped the two IL8 promotor polymorphisms -251A/T and -781C/T and the three amino acid variants M31R, S276T and R335C in IL8RA on 322 children with asthma, 131 infants with severe RSV associated diseases and 270 controls. Statistical analyses made use of the Armitage's trend test for single polymorphisms and FAMHAP for calculations of haplotypes.
We found association of the IL8 polymorphism -781C/T as well as IL8 haplotypes with asthma (p = 0.011 and p = 0.036, respectively). In addition, direct comparison of the asthmatic population with the RSV population revealed significant differences, both for -781C/T alone (p = 0.034) and IL8 haplotypes (p = 0.005). The amino acid variants in IL8RA were evenly distributed in between all three populations.
We conclude from our data that IL8 might play a role in the genetic predisposition to asthma and that these effects are different or even opposite to the effects on severe RSV diseases. Furthermore, IL8RA is unlikely to play a major role in the genetics of either disease.
Interleukin 8 (IL8) is a member of the chemokine family and is produced by a wide range of cell types like monocytes, macrophages, fibroblasts and ceratinocytes. It primarily mediates the activation and migration of neutrophils from peripheral blood into tissue and is involved in the initiation and amplification of inflammatory processes, which occur in the human immune system in response to a wide variety of pathogens . Thus IL8 play an important role in inflammatory lung diseases like bronchial asthma or severe infections caused by respiratory syncytial virus (RSV).
RSV, a single-stranded RNA virus, is involved in at least 70% of cases of infectious infantile bronchiolitis and has been repetitively linked to asthma. It has been hypothesized that severe RSV infection in infancy might lead to the development of recurrent wheezing and/or bronchial asthma [2, 3], and consequently a common genetic background of both diseases has been discussed . According to the current evidence, genetic and environmental factors determine the type of immune response to RSV infection. Furthermore, this response may affect the development of control mechanisms in the regulation of airway diseases, mainly bronchial asthma.
Increased concentrations of IL8 have been described in the bronchoalveolar fluid and sputum of asthmatic patients . In addition, repeated administration of IL8 into the airways induces bronchial hyperreactivity in guinea pigs [6, 7]. Genetic association of IL8 has been described with asthma  and RSV bronchiolitis [9, 10].
IL8 binds with high affinity to two different receptors: IL8 receptor alpha (IL8RA, CXCR1) and beta (IL8RB, CXCR2). These closely related proteins are members of the superfamily of receptors, which couple to guanine nucleotide binding proteins. IL8RA is localized on chromosome 2q35 , where linkage to total serum IgE levels in asthmatics has been described . In addition, association of IL8RA polymorphisms has recently been described with asthma and chronic obstructive pulmonary disease .
We were interested in the relationship between severe RSV infection and/or bronchial asthma and IL8 and IL8RA polymorphisms in the German population. We chose to study two IL8 promoter polymorphisms (-251A/T and -781C/T) and three amino acid variants in IL8RA (M31R, S276T and R335C), which are located in the N-terminus of the protein, in the third extracellular loop and in the C-terminus of the protein respectively. The selection of the IL8 polymorphisms was based on previous studies in our asthmatic and control populations, in which these polymorphisms were shown to be most informative .
Materials and methods
322 children with bronchial asthma (aged 5 to 18 years) were recruited from the South-Western part of Germany between July 2000 and January 2005. All probands were characterized at the University Children's Hospital, Freiburg, Germany using a standardized clinical protocol. An extended medical history was recorded including the occurrence and duration of wheezing symptoms; previous and acute medications; severity of previous asthma attacks; previous allergic rhinitis or conjunctivitis; atopic dermatitis and any family history of allergic diseases.
The diagnosis was based on a clear-cut history of asthmatic symptoms; the use of anti-asthmatic medication and the presence of bronchial hyper-reactivity. The anti-asthmatic drugs included typical betamimetics like salbutamol and standard corticosteroids used in asthma treatment like budesonide. Bronchial hyper-reactivity was defined as a fall in forced respiratory volume in one second (FEV1) by at least 15% in histamine testing or exercise provocation, using standard protocols . The exact recruitment procedure has been described in detail previously .
Population of children with severe RSV infection
This population was recruited at the University Children's Hospital, Freiburg, Germany and also in the Community Children's Hospital, St. Josef's Hospital, Freiburg. Infants and children were eligible when hospitalized due to RSV infection between September 1998 and March 2005 at an age of less than 2 years. RSV infection was detected by antigen test and/or RSV-specific PCR . According to the case definition, children had symptoms of bronchiolitis, for example wheezing and tachypnoe and needed either supplementary oxygen and/or gavage feeding and/or intravenous fluids. Children with congenital heart defects, immune deficiency or chromosomal aberrations were excluded. DNA samples were collected either by blood taking or buccal smears with sterile cotton sticks. In total 131 children were included in this study.
270 randomly chosen probands, aged 19 to 40 years, served as controls. They originated from the same area in the South-Western part of Germany. No medical history was taken and no medical testing was performed on controls.
DNA was extracted from peripheral blood leucocytes or buccal smears following standard protocols and column purified (DNA midikit, Qiagen, Germany). The two IL8 polymorphisms (-251A/T and -781C/T) were typed as described previously .
The three IL8R polymorphisms were typed by means of restriction fragment length polymorphism (RFLP):
Met31Arg (rs16858811) was typed using the primer pair 5'-TGAAGATTACAGGCCCTGTA-3' and 5'-AAATCCAGCCATTCACCTTG-3'. Following PCR, the product was digested with two units of BglI (Fermentas) at 37° over night and the fragments were resolved on a 4% agarose gel.
Ser276Thr (rs16858809) was typed using the primer pair 5'-TCACCCTGCGTACACTGTTT-3' and 5'-GCCAAGAACTCCTTGCTGAC-3. Following PCR, the product was digested with one unit of Alw261 (Fermentas) at 37°C over night and the fragments were resolved on a 4% agarose gel.
Arg335Cys (rs16858808) was typed using the primer pair 5'-AGGAGTTCTTGGCACGTGAT -3' and 5'-AATGATGGTGCTTCGTTTCC-3'. Following PCR, the product was digested with one unit of DpnII (NEB) at 37°C over night and the fragments were resolved on 4% agarose gel.
For each polymorphism, three controls (homozygous wild type, heterozygous and homozygous mutation) were sequenced by the dideoxy chain termination method , using the Big Dye Terminator cycle sequencing kit on an ABI 310 sequencer (Applied Biosystems). All the following studies included these reference individuals.
Association analysis was performed for each polymorphism using Armitage's Trend Test. This test takes into account the individuals' genotypes rather than just the alleles, following the guidelines given by Sasieni , as implemented in the program Finetti (Thomas F. Wienker, unpublished data; http://ihg.gsf.de/cgi-bin/hw/hwa1.pl and http://ihg.gsf.de/linkage/download/finetti.zip). Hardy Weinberg equilibrium (HWE) was calculated for each polymorphism in all three populations using also the program Finetti. In addition to analyses based on single polymorphisms, we performed haplotype frequency estimations using the program FAMHAP . The extent of linkage disequilibrium between polymorphisms has been calculated by Arlequin.
The collection of blood and the experimental procedures were approved by the Ethical Committee of the University of Freiburg. A statement of informed consent was signed by all participants; or in the case of children, signed by their parents.
Frequency and HWE of the polymorphisms within the three populations.
IL8 rs4073 (-251A/T)
IL8 rs2227306 (-781C/T)
IL8RA rs16858811 (M31R)
IL8RA rs16858809 (S276T)
IL8RA rs16858808 (R335C)
Genotype distribution and p-values for association
p-values for association
IL8 rs4073 (-251A/T)
64; 148; 101
26; 73; 34
70; 124; 74
IL8 rs2227306 (-781C/T)
123; 147; 48
37; 62; 27
84; 124; 61
IL8RA rs16858811 (M31R)
299; 20; 0
128; 7; 0
245; 25; 0
IL8RA rs16858809 (S276T)
239; 30; 0
121; 14; 0
IL8RA rs16858808 (R335C)
298; 21; 0
127; 7; 0
246; 23; 1
The two polymorphisms within IL8 were in very tight linkage disequilibrium in all populations (p = 0.00000 for all possible pairs). Thus we did not perform Bonferroni correction for multiple testing as it would be far too conservative in this case. In IL8RA M31R and R35C were transmitted together (p < 0.0001 for all populations).
Frequency of the haplotype within the three populations.
1 1 1
1 2 1
2 1 2
Results of the haplotype analyses using FAMHAP.
So far, only few studies have investigated the impact of polymorphisms within the IL8 signaling pathway on the genetic background of severe RSV associated diseases or bronchial asthma. The IL8 pathway includes IL8 itself, its two receptor chains IL8RA and IL8RB and its degradative enzyme aminopeptidase N . In a previous study, we have shown that IL8 polymorphisms are in association with bronchial asthma in the German population using 230 asthmatic children and 270 randomly chosen controls . Furthermore, we hypothesized that polymorphisms within IL8 have opposite effects on the development of asthma and severe RSV infections. The hypothesis was based on the observation that the -251T allele was more common in patients with asthma than in controls. In contrast, two studies from Hull and colleagues have demonstrated that the opposite allele, that is -251A, is associated with severe RSV infection in the English population [9, 10].
Thus the first aim of the current study was to test whether our initial hypothesis of an opposite role of IL8 polymorphisms on asthma and RSV infections holds in a population of German children with severe RSV associated diseases. Second, we wanted to verify the association between bronchial asthma and IL8 polymorphisms in an extended asthmatic population (increased by 90 asthmatic children to 320 probands). Thirdly, we extended our investigation to include IL8RA as recently association of asthma and chronic obstructive pulmonary disease with this gene has been reported in another German samples .
In the here presented study, the polymorphisms -251A/T and -781C/T within IL8 showed no association with severe RSV associated diseases - neither in analyses of single polymorphisms nor in haplotype analyses. This might suggest that IL8 does not play a major role in the development of severe RSV infections in the German population. These findings are in contrast to the above mentioned studies of Hull et al. [9, 10]. The discrepancy could be due to several reasons: The infants included in the study of Hull et al. were younger than in our study. Furthermore, the inclusion criteria differed slightly between both studies, for example, Hull and colleagues included children with pre-existing heart diseases, whereas we excluded those children. Finally, though the English and German population represent both Caucasians it is well known that the genetic predisposition to allergic diseases are at least partially different between Germans and English people .
The association between bronchial asthma and -781C/T within IL8 could be confirmed in an extended asthmatic population (p = 0.011), whereas the association with the second IL8 polymorphism -251A/T and asthma became weaker and was no longer statistically significant (p = 0.087). This might be in accordance to one study, showing that -251A/T has no functional impact, whereas the base pair substitution C to T at position -781 within the IL8 promotor enhances the binding of transcription factors and thus is probably more important in the genetic regulation of IL8 expression .
Furthermore, a direct comparison of the asthmatic population with the RSV population revealed significant differences, both for -781C/T alone (p = 0.034) as well as in the haplotype analyses (p = 0.005). These results may support our initial hypothesis, that polymorphisms within IL8 have opposite effects in the pathophysiology of asthma and RSV associated diseases. However, one should notice, that the allelic frequencies of the polymorphisms did not markedly differ between controls and children with severe RSV infections. Thus the positive association might merely reflect the fact that the genotype frequencies in asthmatics differ from controls.
In contrast to Stemmler et al, who found that the IL8RA polymorphisms M13R and R335C were significantly associated with bronchial asthma , we found no association of these polymorphisms neither with asthma nor severe RSV associated diseases. Again the conflicting results might be due to different inclusion criteria. The study by Stemmler et al. used 68 adult patients and 130 children with asthma whereas we used exclusively children with asthma. The "adult phenotype" of asthma is quite different from the asthmatic phenotype in children. For example pediatric asthma is much more often allergic than asthma in adults. Thus it might not be surprising that the genetic background of asthma differs between adults and children . Furthermore, the size of our asthmatic study population was larger than the population of Stemmler et al. (198 asthmatic patients versus 320 patients). Thus the significant result in their study might just reflect a type 1 error. However, as the risk factor conferred by a single gene is quite small in complex genetic diseases like asthma, it is also possible that we missed true association in our population due to a type 2 error.
We conclude from our data, that IL8 might play a role in the genetic predisposition to bronchial asthma and that these effects are different, or maybe even opposite to the effects of the same polymorphisms on severe RSV associated diseases. In contrast IL8RA polymorphisms do not play a major role, neither in the development of severe RSV infections nor in asthma.
This project was supported by grants from the Deutsche Forschungsgemeinschaft (DFG HE 3123/3-1 and DFG HE 3123/4-2). The recruitment of asthmatic children was partially supported by a grant from the NIH (NIH R01 HL66533-01).
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