Polymorphisms of interferon-γ gene CA-repeat and interleukin-10 promoter region (-592A/C) in Japanese type I diabetes

被引:37
作者
Tegoshi, H
Hasegawa, G [1 ]
Obayashi, H
Nakano, K
Kitagawa, Y
Fukui, M
Matsuo, S
Deguchi, M
Ohta, M
Nishimura, M
Nakamura, N
Yoshikawa, T
机构
[1] Kyoto Prefectural Univ Med, Dept Internal Med 1, Kamikyo Ku, Kyoto 6020841, Japan
[2] Kyoto Second Res Cross Hosp, Dept Pediat, Kyoto, Japan
[3] Kyoto Second Res Cross Hosp, Dept Internal Med, Kyoto, Japan
[4] Kobe Pharmaceut Univ, Dept Clin Chem, Kobe, Hyogo 658, Japan
[5] Univ Tokushima, Sch Med, Dept Neurol, Tokushima 770, Japan
关键词
interferon-gamma; interleukin-10; interferon-gamma CA-repeat polymorphism; IL-10 promoter polymorphism; type I diabetes mellitus;
D O I
10.1016/S0198-8859(01)00363-9
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We investigated the association of the polymorphisms of interferon-gamma gene (IFNG) CA-repeat and IL-10-592A/C with clinical heterogeneity of type I diabetes as well as susceptibility to type I diabetes. Two hundred seven Japanese type I diabetic patients and 160 healthy control subjects were studied in this case-control study. No significant differences of global IFNG allele frequencies were found between controls and type I diabetic patients, and between each subgroup of the patients and controls. When compared with controls, the a12 allele was increased in the patients with age at onset <25 years p 0.0241, p(c) = 0.1205), and a significant increased frequency of the a12 positive genotype was observed in the patients with age at onset <25 years (p(c) = 0.0121). There were no differences of IL-10-592 genotype and allele frequencies between controls and type I diabetes. However, the frequency of the -592*C allele was significantly increased in the patients with highly positive-GADab compared with controls (p(c) = 0.0060) or compared with the GADab-negative type I patients (p(c) = 0.0276). These results suggest that the IFNG CA-repeat and the IL-10-592A/C polymorphisms are not strong determinants of susceptibility to the development of type I diabetes in Japanese individuals. However, both the IFNG CA-repeat and the IL-10-592A/C polymorphisms are associated with clinical heterogeneity in type I diabetes. Human Inmumology 63, 121-128 (2002), (C) American Society for Histocompatibility and Immunogenetics, 2002. Published by Elsevier Science Inc.
引用
收藏
页码:121 / 128
页数:8
相关论文
共 39 条
[1]   T helper type 1 and 2 cytokines mediate the onset and progression of type I (insulin-dependent) diabetes [J].
Almawi, WY ;
Tamim, H ;
Azar, ST .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1999, 84 (05) :1497-1502
[2]   ASSOCIATION OF POLYMORPHISM IN THE INTERFERON-GAMMA GENE WITH IDDM [J].
AWATA, T ;
MATSUMOTO, C ;
URAKAMI, T ;
HAGURA, R ;
AMEMIYA, S ;
KANAZAWA, Y .
DIABETOLOGIA, 1994, 37 (11) :1159-1162
[3]   Islet-specific expression of IL-10 promotes diabetes in nonobese diabetic mice independent of Fas, perforin, TNF receptor-1, and TNF receptor-2 molecules [J].
Balasa, B ;
Van Gunst, K ;
Jung, N ;
Balakrishna, D ;
Santamaria, P ;
Hanafusa, T ;
Itoh, N ;
Sarvetnick, N .
JOURNAL OF IMMUNOLOGY, 2000, 165 (05) :2841-2849
[4]   INTERFERON-GAMMA ENHANCES THE EXPRESSION OF THE MAJOR HISTOCOMPATIBILITY CLASS-I ANTIGENS ON MOUSE PANCREATIC BETA-CELLS [J].
CAMPBELL, IL ;
WONG, GHW ;
SCHRADER, JW ;
HARRISON, LC .
DIABETES, 1985, 34 (11) :1205-1209
[5]   ESSENTIAL ROLE FOR INTERFERON-GAMMA AND INTERLEUKIN-6 IN AUTOIMMUNE INSULIN-DEPENDENT DIABETES IN NOD/WEHI MICE [J].
CAMPBELL, IL ;
KAY, TWH ;
OXBROW, L ;
HARRISON, LC .
JOURNAL OF CLINICAL INVESTIGATION, 1991, 87 (02) :739-742
[6]   INTERCELLULAR-ADHESION MOLECULE-1 IS INDUCED ON ISOLATED ENDOCRINE ISLET CELLS BY CYTOKINES BUT NOT BY REOVIRUS INFECTION [J].
CAMPBELL, IL ;
CUTRI, A ;
WILKINSON, D ;
BOYD, AW ;
HARRISON, LC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (11) :4282-4286
[7]   A GENOME-WIDE SEARCH FOR HUMAN TYPE-1 DIABETES SUSCEPTIBILITY GENES [J].
DAVIES, JL ;
KAWAGUCHI, Y ;
BENNETT, ST ;
COPEMAN, JB ;
CORDELL, HJ ;
PRITCHARD, LE ;
REED, PW ;
GOUGH, SCL ;
JENKINS, SC ;
PALMER, SM ;
BALFOUR, KM ;
ROWE, BR ;
FARRALL, M ;
BARNETT, AH ;
BAIN, SC ;
TODD, JA .
NATURE, 1994, 371 (6493) :130-136
[8]   PREVENTION OF DIABETES IN NOD MICE TREATED WITH ANTIBODY TO MURINE IFN-GAMMA [J].
DEBRAYSACHS, M ;
CARNAUD, C ;
BOITARD, C ;
COHEN, H ;
GRESSER, I ;
BEDOSSA, P ;
BACH, JF .
JOURNAL OF AUTOIMMUNITY, 1991, 4 (02) :237-248
[9]  
DELEPINE M, 1997, AM J HUM GENET, V64, P793
[10]   Interleukin-10 promoter polymorphism predicts initial response of chronic hepatitis C to interferon alfa [J].
Edwards-Smith, CJ ;
Jonsson, JR ;
Purdie, DM ;
Bansal, A ;
Shorthouse, C ;
Powell, EE .
HEPATOLOGY, 1999, 30 (02) :526-530