HLA-DR6 (possibly DRB1*1301) is associated with susceptibility to Takayasu arteritis in Mexicans

被引:25
作者
Girona, E [1 ]
YamamotoFurusho, JK [1 ]
Cutino, T [1 ]
Reyes, P [1 ]
VargasAlarcon, G [1 ]
Granados, J [1 ]
AlarconSegovia, D [1 ]
机构
[1] INST NACL CARDIOL IGNACIO CHAVEZ, DEPT IMMUNOL, MEXICO CITY, DF, MEXICO
关键词
major histocompatibility complex (MHC); HLA antigens; Takayasu arteritis;
D O I
10.1007/BF01747186
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Takayasu arteritis is characterized by a ''pulseless'' condition and occurs frequently in young females from Asian and South American countries. This disease has been found to be linked with major histocompatibility complex (MHC) antigens in Japanese individuals. In the present study we compared gene frequencies of class I, class II, and class III MHC genotypes in patients with Takayasu arteritis and ethnically matched healthy controls. Serological typing was confirmed by molecular typing at the DNA level. We found significant increases in the frequencies of human leucocyte antigen (HLA)-DR6 and HLA-B62 in patients compared to the healthy controls (P corrected [C] = 0.0007, relative risk [RR] = 5.08; PC = 0.05, RR = 3.13 respectively). However, since the number of patients was considerably lower than the number of controls this can be considered as a tendency and not a true association. On the other hand, we found a significantly decreased frequency of HLA-DR4 in patients compared to healthy controls (PC = 0.04, RR = 0.34). At the DNA level, all DRG-positive individuals were HLA-DRB1*1301 whereas controls were HLA-DRB1*1301 (4.2%). Takayasu arteritis in Mexicans is probably associated with the HLA-DRG (DRB1*1301) gene.
引用
收藏
页码:277 / 280
页数:4
相关论文
共 20 条
[1]   INHERITED STRUCTURAL POLYMORPHISM IN HUMAN C2 - EVIDENCE FOR GENETIC LINKAGE BETWEEN C2 AND BF [J].
ALPER, CA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1976, 144 (04) :1111-1115
[2]   GENETIC POLYMORPHISM IN HUMAN GLYCINE-RICH BETA-GLYCOPROTEIN [J].
ALPER, CA ;
BOENISCH, T ;
WATSON, L .
JOURNAL OF EXPERIMENTAL MEDICINE, 1972, 135 (01) :68-&
[3]   SERUM COMPLEMENT SUPERGENES OF THE MAJOR HISTOCOMPATIBILITY COMPLEX IN MAN (COMPLOTYPES) [J].
ALPER, CA ;
RAUM, D ;
KARP, S ;
AWDEH, ZL ;
YUNIS, EJ .
VOX SANGUINIS, 1983, 45 (01) :62-67
[4]   INHERITED STRUCTURAL POLYMORPHISM OF THE 4TH COMPONENT OF HUMAN-COMPLEMENT [J].
AWDEH, ZL ;
ALPER, CA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1980, 77 (06) :3576-3580
[5]   MAJOR HISTOCOMPATIBILITY COMPLEX - GENETICS AND BIOLOGY .1. [J].
BACH, FH ;
VANROOD, JJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1976, 295 (15) :806-813
[6]   MAJOR HISTOCOMPATIBILITY COMPLEX - GENETICS AND BIOLOGY .2. [J].
BACH, FH ;
VANROOD, JJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1976, 295 (16) :872-878
[7]  
BODMER JG, 1977, HISTOCOMPATIBILITY T, P35
[8]  
BOYUM A, 1968, SCAND J CLIN LAB INV, VS 21, P31
[9]   PULSELESS DISEASE - A PRELIMINARY CASE REPORT [J].
CACCAMISE, WC ;
WHITMAN, JF .
AMERICAN HEART JOURNAL, 1952, 44 (04) :629-633
[10]  
Dong R P, 1992, Heart Vessels Suppl, V7, P73, DOI 10.1007/BF01744548