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Influence of Promoter Variants of Interleukin‐10, Interleukin‐9, and Tumor Necrosis Factor–α Genes on Respiratory Syncytial Virus Bronchiolitis
Author(s) -
Barbara Hoebee,
Louis Bont,
Edwin Rietveld,
Marijke van Oosten,
Hennie M. Hodemaekers,
Nico Nagelkerke,
Herman J. Neijens,
Jan L. L. Kimpen,
Tjeerd G. Kimman
Publication year - 2004
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/380908
Subject(s) - bronchiolitis , odds ratio , immunology , single nucleotide polymorphism , allele , pathogenesis , medicine , genotype , gastroenterology , biology , virus , genetics , gene
Previously, we reported genetic associations between severe respiratory syncytial virus (RSV) bronchiolitis in infants and polymorphisms in the interleukin (IL)-4 and IL-4 receptor alpha (IL-4Ralpha) genes, providing evidence for involvement of T helper type 2 cytokines in the pathogenesis of RSV bronchiolitis. We expanded our studies to polymorphisms in genes encoding IL-9, IL-10, and tumor necrosis factor (TNF)-alpha, using both a transmission/disequilibrium test and a case-control approach. Children homozygous for the IL-10 -592C or -592A allele had a higher risk of hospitalization for RSV bronchiolitis than did heterozygous carriers (odds ratio [OR], 1.73 vs. 2.55; 95% confidence interval [CI], 1.13-2.66 vs. 1.21-5.39). In children hospitalized at < or =6 months of age, a significant association between RSV bronchiolitis and the IL-10 -592C allele was found (OR, 1.61; 95% CI, 1.10-2.35). No significant associations of TNF-alpha and IL-9 polymorphisms with RSV bronchiolitis were observed. We also explored the interactions between different polymorphisms and found an interaction between the IL-4Ralpha Q551R and IL-10 C-592A polymorphisms.

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