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Interaction betweenCD14−159C>T polymorphism andHelicobacter pyloriis associated with serum total immunoglobulin E

Authors :
Mikko Hurme
Mikael Knip
Tanja Pessi
Merja Helminen
Tapio Seiskari
Heikki Hyöty
Miia Virta
Anita Kondrashova
Source :
Clinical & Experimental Allergy. 38:1929-1934
Publication Year :
2008
Publisher :
Wiley, 2008.

Abstract

Summary Background Total serum IgE is regulated by both environmental and genetic factors. Association and linkage studies have suggested a role of CD14−159C>T polymorphism in the regulation of serum total IgE, but the results have been contradictory. It seems that gene–environment interactions are involved in this regulation. Objective The aim of this study was to examine the possible gene–environment interactions among Toxoplasma gondii, Helicobacter pylori, CD14−159C>T and Toll-like receptor (TLR) 4+896A>G polymorphism on serum total IgE. For this study, we expanded the scope of our earlier comparison of allergic sensitization and microbial load between Finland and Russian Karelia by studying the CD14−159C>T and TLR4+896A>G polymorphism in a cohort of Russian Karelian children. Methods For this study, CD14−159C>T and TLR4+896A>G polymorphisms were analysed in 264 healthy Russian Karelian children. Serum total IgE levels and H. pylori and T. gondii antibodies were also measured. Results We constructed a multiway anova model to analyse the gene–environment interactions among T. gondii seropositivity, H. pylori seropositivity, CD14−159C>T and TLR4+896A>G polymorphisms on serum total IgE. The model showed that there was an interaction between the CD14−159 allele T carrier status and H. pylori antibodies on serum total IgE (P=0.004). No other interactions were found. Conclusion Our results further emphasize the role of gene–environment interaction in the regulation of serum total IgE.

Details

ISSN :
13652222 and 09547894
Volume :
38
Database :
OpenAIRE
Journal :
Clinical & Experimental Allergy
Accession number :
edsair.doi.dedup.....264df607c450837e5b265b9d2a0b462f
Full Text :
https://doi.org/10.1111/j.1365-2222.2008.03103.x