Human leukocyte antigen class II alleles in Caucasian women with primary biliary cirrhosis

被引:40
作者
Mullarkey, ME
Stevens, AM
McDonnell, WM
Loubière, LS
Brackensick, JA
Pang, JM
Porter, AJ
Galloway, DA
Nelson, JL
机构
[1] Fred Hutchinson Canc Res Ctr, Immunogenet Program, Seattle, WA 98109 USA
[2] Univ Washington, Dept Pediat, Seattle, WA 98195 USA
[3] Univ Washington, Div Rheumatol, Seattle, WA 98195 USA
[4] Fred Hutchinson Canc Res Ctr, Canc Biol Program, Seattle, WA 98109 USA
[5] Western Washington Med Grp, Everett, WA USA
来源
TISSUE ANTIGENS | 2005年 / 65卷 / 02期
关键词
autoimmune disease; HLA alleles; primary biliary cirrhosis;
D O I
10.1111/j.1399-0039.2005.00351.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In the current study, we investigated human leukocyte antigen (HLA) class II alleles in Caucasian women with primary biliary cirrhosis (PBC), a disease that preferentially affects women. Alleles of DRB1, DQA1, and DQB1 were determined by DNA-based HLA typing for women with PBC (n = 72) and healthy women (n = 381). All study subjects were Caucasian. HLA DRB1*08 was significantly increased in women with PBC compared to healthy women. The increase was primarily due to the DRB1*0801 allele, also the most common DRB1*08 allele among controls. DQB1*04 and DQA1*0401 were significantly increased. DRB1*1501, DQA1*0102, and DQB1*0602 were associated with decreased risk. Analyses conducted comparing parous women with PBC to parous healthy women (n = 68 and n = 282, respectively) yielded similar significant results. Although the DRB1*08-DQA1*0401-DQB1*04 haplotype was significantly associated with PBC, consistent with other studies, this haplotype nevertheless represented only 19% (14/72) of all PBC patients and can account for only a minority of the risk of PBC.
引用
收藏
页码:199 / 205
页数:7
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