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Depner, M.* ; Kormann, M.S.* ; Klopp, N. ; Illig, T. ; Vogelberg, C.* ; Weiland, S.K.* ; von Mutius, E.* ; Combadière, C.* ; Kabesch, M.*

CX3CR1 polymorphisms are associated with atopy but not asthma in German children.

Int. Arch. Allergy Immunol. 144, 91-94 (2007)
DOI PMC
Open Access Green as soon as Postprint is submitted to ZB.
Chemokines and their receptors are involved in many aspects of immunity. Chemokine CX3CL1, acting via its receptor CX3CR1, regulates monocyte migration and macrophage differentiation as well as T cell-dependent inflammation. Two common, nonsynonymous polymorphisms in CX3CR1 have previously been shown to alter the function of the CX3CL1/CX3CR1 pathway and were suggested to modify the risk for asthma. Using matrix-assisted laser desorption/ionization time-of-flight technology, we genotyped polymorphisms Val249Ile and Thr280Met in a cross-sectional population of German children from Munich (n = 1,159) and Dresden (n = 1,940). For 249Ile an odds ratio of 0.77 (95% confidence interval 0.63-0.96; p = 0.017) and for 280Met an odds ratio of 0.71 (95% confidence interval 0.56-0.89; p = 0.004) were found with atopy in Dresden but not in Munich. Neither polymorphism was associated with asthma. Thus, amino acid changes in CX3CR1 may influence the development of atopy but not asthma in German children. Potentially, other factors such as environmental effects may modify the role of CX3CR1 polymorphisms.
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Publication type Article: Journal article
Document type Scientific Article
Corresponding Author
Keywords Asthma; Atopy; Chemokine; Polymorphism; CX3CR1
ISSN (print) / ISBN 1018-2438
e-ISSN 1423-0097
Quellenangaben Volume: 144, Issue: 1, Pages: 91-94 Article Number: , Supplement: ,
Publisher Karger
Publishing Place Basel ; Freiburg [Breisgau] ; Paris ; London ; New York ; Bangalore ; Bangkok ; Singapore ; Tokyo ; Sydney
Non-patent literature Publications
Reviewing status Peer reviewed