Genetic regulation of Dermatophagoides pteronyssinus-specific Ig E responsiveness: A genome-wide multipoint linkage analysis in families recruited through 2 asthmatic sibs

Nobuyuki Hizawa, Linda R. Freidhoff, Yen Feng Chiu, Eva Ehrlich, Craig A. Luehr, Jennifer L. Anderson, David L. Duffy, Georgia M. Dunston, James L. Weber, Shau Ku Huang, Kathleen C. Barnes, David G. Marsh, Terri H. Beaty

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88 引文 斯高帕斯(Scopus)

摘要

Background: Dermatophagoides pteronyssinus (Der p) is one of the most frequently implicated allergens in atopic diseases. Although HLA could play an important role in the development of the IgE response to the Der p allergens, genetic regulation by non-HLA genes influences certain HLA-associated IgE responses to complex allergens. Objective: To clarify genetic control for the expression of Der p-specific IgE responsiveness, we conducted a genome-wide search for genes influencing Der p-specific IgE antibody levels by using 45 Caucasian and 53 African American families ascertained as part of the Collaborative Study on the Genetics of Asthma (CSGA). Methods: Specific IgE antibody levels to the Der p crude allergen and to the purified allergens Der p l and Der p 2 were measured. Multipoint, nonparametric linkage analysis of 370 polymorphic markers was performed with the GENE-HUNTER program. Results: The best evidence of genes controlling specific IgE response to Der p was obtained in 2 novel regions: chromosomes 2q21-q23 (P = .0033 for Caucasian subjects) and 8p23-p21 (P = .0011 for African American subjects). Three regions previously proposed as candidate regions for atopy, total IgE, or asthma also showed evidence for linkage to Der p-specific IgE responsiveness: 6p21 (P = .0064) and 13q32-q34 (P = 0.0064) in Caucasian subjects and 5q23-q33 (P = 0.0071) in African American subjects. Conclusions: No single locus generated overwhelming evidence for linkage in terms of established criteria and guidelines for a genome-wide screening, which supports previous assertions of a heterogeneous etiology for Der p-specific IgE responsiveness. Two novel regions, 2q21-q23 and 8p23-p21, that were identi-fied in this study merit additional study.

原文英語
頁(從 - 到)436-442
頁數7
期刊Journal of Allergy and Clinical Immunology
102
發行號3
DOIs
出版狀態已發佈 - 1月 1 1998
對外發佈

ASJC Scopus subject areas

  • 免疫學和過敏
  • 免疫學

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