Exclusion of chromosome 11q and the FcεRI-β gene as aetiological factors in allergy and asthma in a population of Dutch asthmatic families

P. J. Amelung, D. S. Postma, J. Xu, D. A. Meyers, E. R. Bleecker

Research output: Contribution to journalArticlepeer-review

27 Scopus citations


Background: The β subunit of the high-affinity receptor for IgE (FcεRI-β) is localized to chromosome 11q13 and has been reported by Cookson et al. to be in close genetic linkage with a gene for atopy. A maternally inherited association was found between the presence of a variant of FcεRI- β, Ile181Leu, and high total serum IgE levels (IgE > 100 IU). In a previous study of 20 Dutch families, we found no evidence for linkage of atopy or bronchial hyperresponsiveness (BHR) to chromosome 11q. Objective: Recently segregation analysis in 92 families has given us evidence for two independent major loci accounting for 78% of the observed variance in total serum IgE levels, and linkage analysis using both sib-pair and LOD score methods has identified one major locus for regulation of IgE levels and BHR near the cytokine gene complex on chromosome 5q. The Objective: of this study is to pursue the identification of the second major locus. Methods: We have studied markers in the area of the high affinity IgE receptor (FcεRI-β) on chromosome 11q (D11S1314, FcεRI-β and D11S987) in 83 families for whom DNA was available. Furthermore, our families have been examined for variance in the FcεRI-β gene, specifically for Leu 181 and Leu 181/Leu 183 mutations. Results: By sib-pair analysis, there is no evidence for linkage of total serum IgE levels or number of positive skin tests to these markers in our population. Similar negative results were obtained for affected sib-pair analysis of BHR, with the exception of D11S1314, which was significant at P = 0.046. The FcεRI-β gene in 36 female probands, 44 male probands and 46 female spouses was sequenced for these mutations. For each of these 126 individuals sequencing of FcεRI-β demonstrated a wild-type sequence pattern, with no mutations found in anyone, male or female. Conclusion: We are unable to confirm the presence of significant mutations in FcεRI-β gene in our population, and we cannot confirm that the FcεRI-β gene is crucial to the pathogenesis of allergic inflammation in asthma.

Original languageEnglish (US)
Pages (from-to)397-403
Number of pages7
JournalClinical and Experimental Allergy
Issue number4
StatePublished - 1998
Externally publishedYes


  • Asthma
  • Bronchial hyperresponsiveness
  • Chromosome 11
  • IgE
  • IgE receptor
  • Linkage
  • Skin-prick tests

ASJC Scopus subject areas

  • Immunology and Allergy
  • Immunology


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