Evaluation of the CD14 C-159 T polymorphism in the German Multicenter Allergy Study cohort

被引:98
作者
Sengler, C
Haider, A
Sommerfeld, C
Lau, S
Baldini, M
Martinez, F
Wahn, U
Nickel, R
机构
[1] Humboldt Univ, Charite, Dept Pediat Pneumol & Immunol, D-13353 Berlin, Germany
[2] Univ Arizona, Dept Pediat, Tucson, AZ 85721 USA
关键词
atopy; CD14; genetics; IgE;
D O I
10.1046/j.1365-2222.2003.01549.x
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Background Multiple genetic studies have shown linkage of atopy-related phenotypes to chromosome 5q31. In this region several candidate genes for atopy are localized such as the Th2 cytokines IL-4, IL-5 and IL-13, but also CD14, a receptor for LPS. Recently, a functional CD14 promoter polymorphism was related to total and specific IgE responsiveness. Objective The aim of our study was to evaluate the role of this single nucleotide polymorphism (SNP) in a large German birth cohort. Methods Atopy-related phenotypes were longitudinally carefully evaluated in over 800 children from birth to the age of 10 years. Yearly visits included standardized interviews, physical examinations and determination of total and specific IgE antibodies. Pulmonary function tests and histamine provocations were performed at the age of seven. Eight-hundred and seventy-two children of the Multicenter Allergy Study (MAS) cohort were genotyped using melting curve and restriction digest analyses. Results CD14-159 allele frequencies were consistent with previous reports, however, no association of the SNP with asthma, atopic dermatitis, allergic rhinitis, total or specific IgE levels could be observed. Conclusion The CD14-159 SNP might not play a major role in the development of atopy in German children.
引用
收藏
页码:166 / 169
页数:4
相关论文
共 13 条
[1]   A polymorphism* in the 5′ flanking region of the CD14 gene is associated with circulating soluble CD14 levels and with total serum immunoglobulin E [J].
Baldini, M ;
Lohman, IC ;
Halonen, M ;
Erickson, RP ;
Holt, PG ;
Martinez, FD .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 1999, 20 (05) :976-983
[2]  
Bergmann RL, 1998, CLIN EXP ALLERGY, V28, P965
[3]   Early childhood infectious diseases and the development of asthma up to school age: a birth cohort study [J].
Illi, S ;
von Mutius, E ;
Lau, S ;
Bergmann, R ;
Niggemann, B ;
Sommerfeld, C ;
Wahn, U .
BMJ-BRITISH MEDICAL JOURNAL, 2001, 322 (7283) :390-395
[4]   Association of a promoter polymorphism of the CD14 gene and atopy [J].
Koppelman, GH ;
Reijmerink, NE ;
Stine, OC ;
Howard, TD ;
Whittaker, PA ;
Meyers, DA ;
Postma, DS ;
Bleecker, ER .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2001, 163 (04) :965-969
[5]   Development of seasonal allergic rhinitis during the first 7 years of life [J].
Kulig, M ;
Klettke, U ;
Wahn, V ;
Forster, J ;
Bauer, CP ;
Wahn, U .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2000, 106 (05) :832-839
[6]   Early exposure to house-dust mite and cat allergens and development of childhood asthma: a cohort study [J].
Lau, S ;
Illi, S ;
Sommerfeld, C ;
Niggemann, B ;
Bergmann, R ;
von Mutius, E ;
Wahn, U .
LANCET, 2000, 356 (9239) :1392-1397
[7]   A common single nucleotide polymorphism in the CD14 promoter decreases the affinity of Sp protein binding and enhances transcriptional activity [J].
LeVan, TD ;
Bloom, JW ;
Bailey, TJ ;
Karp, CL ;
Halonen, M ;
Martinez, FD ;
Vercelli, D .
JOURNAL OF IMMUNOLOGY, 2001, 167 (10) :5838-5844
[8]   Evidence for linkage of chromosome 12q15-q24.1 markers to high total serum IgE concentrations in children of the German Multicenter Allergy Study [J].
Nickel, R ;
Wahn, U ;
Hizawa, N ;
Maestri, N ;
Duffy, DL ;
Barnes, KC ;
Beyer, K ;
Forster, J ;
Bergmann, R ;
Zepp, F ;
Wahn, V ;
Marsh, DG .
GENOMICS, 1997, 46 (01) :159-162
[9]  
Sengler C, 2001, RESP RES, V3
[10]   RECEPTOR-DEPENDENT MECHANISMS OF CELL STIMULATION BY BACTERIAL-ENDOTOXIN [J].
ULEVITCH, RJ ;
TOBIAS, PS .
ANNUAL REVIEW OF IMMUNOLOGY, 1995, 13 :437-457