Association between type 1 diabetes mellitus with cytotoxic T lymphocyte associated 4 (CTLA-4) in Tunisian population.

被引:13
作者
Abid, HK
Hmida, S
Smaoui, N
Kaabi, H
Abid, A
Chaabouni, H
Boukef, K
Nagati, K
机构
[1] Inst Natl Nutr & Technol Alimentaire, Tunis 1006, Tunisia
[2] Ctr Natl Transfus Sanguine, Tunis 1006, Tunisia
[3] Hop Charles Nicolle, Serv Genet Humaine, Tunis, Tunisia
来源
PATHOLOGIE BIOLOGIE | 2001年 / 49卷 / 10期
关键词
association CTLA-4 gene dimorphism; type; 1; diabetes;
D O I
10.1016/S0369-8114(01)00246-2
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Susceptibility to type I diabetes mellitus is strongly associated with particular HLA class II alleles, However, non HLA genetic factors are likely to be required for the development of disease, The candidate genes include the cytotoxic T lymphocyte associated 4 (CTLA-4) located on chromosome 2q33 and designated (IDDM12), which encodes a cell surface negative signal T molecule providing for activation. We investigated CTLA-4 exon 1 dimorphism in 74 type I patients and a control group of 48 healthy subjects from Tunisia using two methods PCR (polymerase chain reaction) allele specific and polymerase chain reaction restriction fragment length polymorphism (PCR RFLP). The CTLA-4/G allele was found on 68.9% in type I patients as compared to 51.02% in controls (p = 0.002), mostly in homozygous from 43.24% versus 22.45% (p = 0.0058), This results indicate that CTLA-4/G allele was significantly associated with predisposition to type I diabetes In our group from Tunisian population. (C) 2001 Editions scientifiques et medicales Elsevier SAS.
引用
收藏
页码:794 / 798
页数:5
相关论文
共 17 条
[1]   A NEW MEMBER OF THE IMMUNOGLOBULIN SUPERFAMILY - CTLA-4 [J].
BRUNET, JF ;
DENIZOT, F ;
LUCIANI, MF ;
ROUXDOSSETO, M ;
SUZAN, M ;
MATTEI, MG ;
GOLSTEIN, P .
NATURE, 1987, 328 (6127) :267-270
[2]  
BRUNET JF, 1988, IMMUNOL REV, P103
[3]  
COTEN MC, 1977, TISSUE ANTIGENS, V9, P59
[4]   CTLA4 alanine-17 confers genetic susceptibility to Graves' disease and to type 1 diabetes mellitus [J].
Donner, H ;
Rau, H ;
Walfish, PG ;
Braun, J ;
Siegmund, T ;
Finke, R ;
Herwig, J ;
Usadel, KH ;
Badenhoop, K .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1997, 82 (01) :143-146
[5]  
Krokowski M, 1998, DIABETES METAB, V24, P241
[6]  
LINDSTEN T, 1993, J IMMUNOL, V151, P3489
[7]   Insulin-dependent diabetes mellitus (IDDM) is associated with CTLA4 polymorphisms in multiple ethnic groups [J].
Marron, MP ;
Raffel, LJ ;
Garchon, HJ ;
Jacob, CO ;
SerranoRios, M ;
Larrad, MTM ;
Teng, WP ;
Park, Y ;
Zhang, ZX ;
Goldstein, DR ;
Tao, YW ;
Beaurain, G ;
Bach, JF ;
Huang, HS ;
Luo, DF ;
Zeidler, A ;
Rotter, JI ;
Yang, MCK ;
Modilevsky, T ;
Maclaren, NK ;
She, JX .
HUMAN MOLECULAR GENETICS, 1997, 6 (08) :1275-1282
[8]   A SIMPLE SALTING OUT PROCEDURE FOR EXTRACTING DNA FROM HUMAN NUCLEATED CELLS [J].
MILLER, SA ;
DYKES, DD ;
POLESKY, HF .
NUCLEIC ACIDS RESEARCH, 1988, 16 (03) :1215-1215
[9]   The CTLA-4 gene region of chromosome 2q33 is linked to, and associated with, type 1 diabetes [J].
Nistico, L ;
Buzzetti, R ;
Pritchard, LE ;
VanderAuwera, B ;
Giovannini, C ;
Bosi, E ;
Larrad, MTM ;
Rios, MS ;
Chow, CC ;
Cockram, CS ;
Jacobs, K ;
Mijovic, C ;
Bain, SC ;
Barnett, AH ;
Vandewalle, CL ;
Schuit, F ;
Gorus, FK ;
Tosi, R ;
Pozzilli, P ;
Todd, JA .
HUMAN MOLECULAR GENETICS, 1996, 5 (07) :1075-1080
[10]  
Noble JA, 1996, AM J HUM GENET, V59, P1134