Common polymorphisms in the CTLA-4 and CD28 genes at 2q33 are not associated with asthma or atopy

被引:39
作者
Heinzmann, A [1 ]
Plesnar, C [1 ]
Kuehr, J [1 ]
Forster, J [1 ]
Deichmann, KA [1 ]
机构
[1] Univ Freiburg, Univ Childrens Hosp, D-79106 Freiburg, Germany
来源
EUROPEAN JOURNAL OF IMMUNOGENETICS | 2000年 / 27卷 / 02期
关键词
D O I
10.1046/j.1365-2370.2000.00198.x
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Recently, genetic linkage of the chromosomal region 2q33 with asthma has been shown. The genes coding for CD28 and CTLA-4 have been localized to this chromosomal region. CD28 and CTLA-4 have been shown to be involved as an important costimulatory signal in the regulation of allergic inflammation and TH2 cytokine production, and thus both genes are good candidate genes for asthma and atopy. Two common polymorphisms in the CTLA-4 gene and one polymorphism in the CD28 gene found by single-strand conformation polymorphisms (SSCP) analysis and direct genomic sequencing were tested for association with asthma and atopy phenotypes in a population of 260 largely atopic children and young adults. No association was found between any of the three polymorphisms and asthma or atopy phenotypes. The newly described common CD28 polymorphism is situated in the third intron of the gene. We conclude that neither gene is likely to exert a major influence on the development of asthma or atopy in our population. However, it might prove useful to test for association of these polymorphisms with asthma in populations recruited through asthmatic but not necessarily atopic individuals.
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页码:57 / 61
页数:5
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共 31 条
  • [1] THE YIN AND YANG OF T-CELL COSTIMULATION
    ALLISON, JP
    KRUMMEL, MF
    [J]. SCIENCE, 1995, 270 (5238) : 932 - 933
  • [2] MOLECULAR LINKAGE OF THE HUMAN CTLA4 AND CD28 IG-SUPERFAMILY GENES IN YEAST ARTIFICIAL CHROMOSOMES
    BUONAVISTA, N
    BALZANO, C
    PONTAROTTI, P
    LEPASLIER, D
    GOLSTEIN, P
    [J]. GENOMICS, 1992, 13 (03) : 856 - 861
  • [3] DARIAVACH P, 1989, CYTOGENET CELL GENET, V51, P983
  • [4] An Mse I RFLP in the human CTLA4 promotor
    Deichmann, K
    Heinzmann, A
    Bruggenolte, E
    Forster, J
    Kuehr, J
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1996, 225 (03) : 817 - 818
  • [5] DEICHMANN KA, 1996, ALLERGY, P42
  • [6] CTLA-4 gene polymorphism is associated with predisposition to coeliac disease
    Djilali-Saiah, I
    Schmitz, J
    Harfouch-Hammoud, E
    Mougenot, JF
    Bach, JF
    Caillat-Zucman, S
    [J]. GUT, 1998, 43 (02) : 187 - 189
  • [7] Codon 17 polymorphism of the cytotoxic T lymphocyte antigen 4 gene in Hashimoto's thyroiditis and Addison's disease
    Donner, H
    Braun, J
    Seidl, C
    Rau, H
    Finke, R
    Ventz, M
    Walfish, PG
    Usadel, KH
    Badenhoop, K
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1997, 82 (12) : 4130 - 4132
  • [8] CTLA4 alanine-17 confers genetic susceptibility to Graves' disease and to type 1 diabetes mellitus
    Donner, H
    Rau, H
    Walfish, PG
    Braun, J
    Siegmund, T
    Finke, R
    Herwig, J
    Usadel, KH
    Badenhoop, K
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1997, 82 (01) : 143 - 146
  • [9] B7-1 AND B7-2 DO NOT DELIVER IDENTICAL COSTIMULATORY SIGNALS, SINCE B7-2 BUT NOT B7-1 PREFERENTIALLY COSTIMULATES THE INITIAL PRODUCTION OF IL-4
    FREEMAN, GJ
    BOUSSIOTIS, VA
    ANUMANTHAN, A
    BERNSTEIN, GM
    KE, XY
    RENNERT, PD
    GRAY, GS
    GRIBBEN, JG
    NADLER, LM
    [J]. IMMUNITY, 1995, 2 (05) : 523 - 532
  • [10] CD80 costimulation is essential for the induction of airway eosinophilia
    Harris, N
    Peach, R
    Naemura, J
    Linsley, PS
    LeGros, G
    Ronchese, F
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 185 (01) : 177 - 182