MICB microsatellite polymorphism is associated with ulcerative colitis in Chinese population

被引:42
作者
Lu, Min
Xia, Bing
Li, Jin
Ye, Mei
Zhang, Xiaolian
Tan, Qinquan
机构
[1] Wuhan Univ, Zhongnan Hosp, Dept Internal Med & Geriatr, Wuhan 430071, Peoples R China
[2] Wuhan Univ, Zhongnan Hosp, Res Ctr Digest Dis, Wuhan 430071, Peoples R China
[3] Wuhan Univ, Sch Med, Key Lab Allergy & Immune Related Dis, Wuhan, Peoples R China
关键词
ulcerative colitis; MHC class I chain-related gene B; MHC class I chain-related gene A; MICB-CA18; MICA-A5.1; microsatellite polymorphism; Chinese;
D O I
10.1016/j.clim.2006.03.001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
The MHC class I-related molecules A and B (MICA and MICB) are stress-inducible cell surface antigens that are recognized by immunocytes bearing the receptor NKG2D, including intestinal epithelial V delta 1 y delta T cells, which may play a role in immunological reaction in intestinal mucosa. The present study was aimed to investigate the association of the microsatellite polymorphisms in the intron 1 of MICB and the MICA-MICB haplotype with the susceptibility to ulcerative colitis (UC) in Chinese population. The microsatellite polymorphisms of MICB were genotyped in unrelated 127 Chinese patients with UC and 193 ethnically matched healthy controls by a semiautomatic fluorescently labeled PCR method. All the subjects were the Chinese with Han nationality. The frequency of MICB-CA18 was significantly higher in UC patients compared with the healthy controls (14.0% vs. 5.8%, P = 0.0016, Pc 0.024, OR = 2.637, 95% Cl: 1.443-4.820) and was increased in the female patients compared with the female healthy controls (18.3% vs. 4.1%, P = 0.0006, Pc = 0.0080, OR = 5.224, 95% CI: 1.940-14.069). Thus, MICB-CA18 is positively associated with UC and female UC patients in Chinese population. (c) 2006 Elsevier Inc. All. rights reserved.
引用
收藏
页码:199 / 204
页数:6
相关论文
共 42 条
[1]
High resolution MIC genotyping: Design and application to the investigation of inflammatory bowel disease susceptibility [J].
Ahmad, T ;
Marshall, SE ;
Mulcahy-Hawes, K ;
Orchard, T ;
Crawshaw, J ;
Armuzzi, A ;
Neville, M ;
van Heel, D ;
Barnardo, M ;
Welsh, KI ;
Jewell, DP ;
Bunce, M .
TISSUE ANTIGENS, 2002, 60 (02) :164-179
[2]
The MIC gene family [J].
Bahram, S ;
Spies, T .
RESEARCH IN IMMUNOLOGY, 1996, 147 (05) :328-333
[3]
A 2ND LINEAGE OF MAMMALIAN MAJOR HISTOCOMPATIBILITY COMPLEX CLASS-I GENES [J].
BAHRAM, S ;
BRESNAHAN, M ;
GERAGHTY, DE ;
SPIES, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (14) :6259-6263
[4]
HLA-DRB1 and MICA in autoimmunity -: Common associated alleles in autoimmune disorders [J].
Bilbao, JR ;
Martín-Pagola, A ;
De Nanclares, GP ;
Calvo, B ;
Vitoria, JC ;
Vázquez, F ;
Castaño, L .
IMMUNOLOGY OF DIABETES II: PATHOGENESIS FROM MOUSE TO MAN, 2003, 1005 :314-318
[5]
Familial occurrence and inheritance studies in inflammatory bowel disease [J].
Binder, V ;
Orholm, M .
NETHERLANDS JOURNAL OF MEDICINE, 1996, 48 (02) :53-56
[6]
MICA and MICB microsatellite alleles in HLA extended haplotypes [J].
Bolognesi, E ;
D'Alfonso, S ;
Rolando, V ;
Fasano, ME ;
Praticò, L ;
Momigliano-Richiardi, R .
EUROPEAN JOURNAL OF IMMUNOGENETICS, 2001, 28 (05) :523-530
[7]
Inflammatory bowel disease gene hunting by linkage analysis - rationale, methodology, and present status of the field [J].
Brant, SR ;
Shugart, YY .
INFLAMMATORY BOWEL DISEASES, 2004, 10 (03) :300-311
[8]
Replication and extension studies of inflammatory bowel disease susceptibility regions confirm linkage to chromosome 6p (IBD3) [J].
Dechairo, B ;
Dimon, C ;
van Heel, D ;
Mackay, I ;
Edwards, M ;
Scambler, P ;
Jewell, D ;
Cardon, L ;
Lench, N ;
Carey, A .
EUROPEAN JOURNAL OF HUMAN GENETICS, 2001, 9 (08) :627-633
[9]
A COMPARISON OF LINKAGE DISEQUILIBRIUM MEASURES FOR FINE-SCALE MAPPING [J].
DEVLIN, B ;
RISCH, N .
GENOMICS, 1995, 29 (02) :311-322
[10]
MHC class I chain-related gene A-A5•1 allele is associated with ulcerative colitis in Chinese population [J].
Ding, YJ ;
Xia, B ;
Lü, M ;
Zhang, Y ;
Li, J ;
Ye, M ;
Luo, HS ;
Yu, JP ;
Zhang, XL ;
Tan, JQ .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2005, 142 (01) :193-198