MAJOR HISTOCOMPATIBILITY COMPLEX GENES AND SUSCEPTIBILITY TO SYSTEMIC LUPUS-ERYTHEMATOSUS

被引:106
作者
FRONEK, Z
TIMMERMAN, LA
ALPER, CA
HAHN, BH
KALUNIAN, K
PETERLIN, BM
MCDEVITT, HO
机构
[1] STANFORD UNIV,MED CTR,SCH MED,DEPT MICROBIOL & IMMUNOL,STANFORD,CA 94305
[2] HARVARD UNIV,CTR BLOOD RES,SCH MED,BOSTON,MA 02115
[3] UNIV CALIF LOS ANGELES,DEPT MED,DIV RHEUMATOL,LOS ANGELES,CA 90024
[4] UNIV CALIF SAN FRANCISCO,HOWARD HUGHES MED INST,DEPT MED,SAN FRANCISCO,CA 94143
[5] UNIV CALIF SAN FRANCISCO,HOWARD HUGHES MED INST,DEPT MICROBIOL & IMMUNOL,SAN FRANCISCO,CA 94143
来源
ARTHRITIS AND RHEUMATISM | 1990年 / 33卷 / 10期
关键词
D O I
10.1002/art.1780331012
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Susceptibility to systemic lupus erythematosus is associated with major histocompatibility complex (MHC)‐encoded genes. We have used nucleotide sequence analysis to better define the disease‐associated MHC alleles. HLA‐DR2, DQw1, and especially the rare allele DQβ1.AZH confer high relative risk (RR = 14) for lupus nephritis in a Caucasian population of patients. Pilot studies using historical controls suggest that these genes also confer a high risk in non‐Caucasian ethnic groups (RR = 24–78). We have found that DR4 is significantly decreased in patients with lupus nephritis. Fifty percent of the patients with lupus nephritis had either the DQβ1.1, the DQβ1.AZH, or the DQβ1.9 alleles. These alleles share amino acid residues that have been predicted to be the contact points for antigen and the T cell receptor. These HLA alleles appear to have a direct role in the predisposition to lupus nephritis, whereas DR4 may have a “protective” effect. Copyright © 1990 American College of Rheumatology
引用
收藏
页码:1542 / 1553
页数:12
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