CTLA4 polymorphisms in Spanish patients with rheumatoid arthritis

被引:82
作者
Gonzalez-Escribano, MF
Rodriguez, R
Valenzuela, A
Garcia, A
Garcia-Lozano, JR
Nuñez-Roldan, A
机构
[1] Hosp Univ Virgen del Rocio, Serv Inmunol, Serv Andaluz de Salud, Seville 41013, Spain
[2] Hosp Univ Virgen del Rocio, Serv Reumatol, Serv Andaluz de Salud, Seville 41013, Spain
来源
TISSUE ANTIGENS | 1999年 / 53卷 / 03期
关键词
CTLA4; HLA-DR; PCR-ARMS; rheumatoid arthritis;
D O I
10.1034/j.1399-0039.1999.530311.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cytotoxic T-lymphocyte antigen 4 (CTLA4) polymorphisms located in the promotor region at positions -318 (C/T) and in exon 1 (49 A/ G) were investigated in 138 Spanish patients (37 men and 101 women) with rheumatoid arthritis and in 305 ethnically-matched healthy controls, When the allelic and genotypic frequencies corresponding to the CTLA4 -318 position were compared, no significant differences between patients and controls were found. However when the CTLA4 49 A/G polymorphism was analysed, a significant increase of A/G heterozygous individuals among female patients (48.5% vs. 33.8% in controls; P=0.008; OR=2.0) was observed. This increase was absent among males (37.8%, P=NS). Analysis of the CTLA4 49 polymorphism with respect to HLA-DRB1 typing demonstrated a significant increase of A/G heterozygosity in the HLA-DR3-positive patient group compared with HLA-DR3-negative patient group (14/19, 74% vs. 49/119, 41%; P=0.009, OR=4.0). The increase of A/G genotype among HLA-DR3-positive patients was found in both males (4/6, 67%) and females (10/13, 77%), although statistical differences were only reached in the female group. These results provide new insight into this complex association, confirm previous data from other studies, and suggest that the CTLA4 gene could be involved in the pathogenesis of rheumatoid arthritis.
引用
收藏
页码:296 / 300
页数:5
相关论文
共 23 条
[1]  
AHMED SA, 1985, AM J PATHOL, V121, P531
[2]  
ARNETT FC, 1987, ARTHRITIS RHEUM, V31, P315
[3]  
BIGNON JD, 1997, GENETIC DIVERSITY HL, V1, P584
[4]   An Mse I RFLP in the human CTLA4 promotor [J].
Deichmann, K ;
Heinzmann, A ;
Bruggenolte, E ;
Forster, J ;
Kuehr, J .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1996, 225 (03) :817-818
[5]   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
[6]  
FERNANDEZVINA MA, 1997, GENETIC DIVERSITY HL, P596
[7]   THE SHARED EPITOPE HYPOTHESIS - AN APPROACH TO UNDERSTANDING THE MOLECULAR-GENETICS OF SUSCEPTIBILITY TO RHEUMATOID-ARTHRITIS [J].
GREGERSEN, PK ;
SILVER, J ;
WINCHESTER, RJ .
ARTHRITIS AND RHEUMATISM, 1987, 30 (11) :1205-1213
[8]  
HARPER K, 1991, J IMMUNOL, V147, P1037
[9]  
Kawasaki E-S., 1990, PCR PROTOCOLS GUIDE
[10]   CYTOTOXIC T-LYMPHOCYTE-ASSOCIATED MOLECULE-4, A HIGH AVIDITY RECEPTOR FOR CD80 AND CD86, CONTAINS AN INTRACELLULAR-LOCALIZATION MOTIF IN ITS CYTOPLASMIC TAIL [J].
LEUNG, HT ;
BRADSHAW, J ;
CLEAVELAND, JS ;
LINSLEY, PS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (42) :25107-25114