Evidence for genetic regulation of susceptibility to toxoplasmic encephalitis in AIDS patients

被引:87
作者
Suzuki, Y
Wong, SY
Grumet, FC
Fessel, J
Montoya, JG
Zolopa, AR
Portmore, A
SchumacherPerdreau, F
Schrappe, M
Koppen, S
Ruf, B
Brown, BW
Remington, JS
机构
[1] PALO ALTO MED FDN,RES INST,DEPT IMMUNOL & INFECT DIS,PALO ALTO,CA 94301
[2] STANFORD UNIV,SCH MED,DEPT MED,DIV INFECT DIS & GEOG MED,STANFORD,CA 94305
[3] STANFORD UNIV,SCH MED,DEPT PATHOL,DEPT HLTH RES & POLICY,STANFORD,CA 94305
[4] SAN FRANCISCO KAISER PERMANENTE,SAN FRANCISCO,CA
[5] FREE UNIV BERLIN,KLINIKUM RUDOLF VIRCHOW,DEPT MED,W-1000 BERLIN,GERMANY
[6] UNIV COLOGNE,DEPT INTERNAL MED,INST MED MIKROBIOL,W-5000 COLOGNE,GERMANY
关键词
D O I
10.1093/infdis/173.1.265
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The frequency of HLA-DQ antigens in AIDS patients with toxoplasmic encephalitis (TE) were examined. HLA-DQ3 was significantly more frequent in white North American AIDS patients with TE (85.0%) than in the general white population (51.8%; P = .007, corrected P = .028) or randomly selected control AIDS patients who had not developed TE (40.0%; P = .016). In contrast, the frequency of HLA-DQ1 was lower in TE patients than in healthy controls (40.0% vs. 66.5%, P = .027), but this difference did not reach statistical significance when corrected for the number of variables tested (corrected P = .108 for the general white population). HLA-DQ3 thus appears to be a genetic marker of susceptibility to development of TE in AIDS patients, and DQ1 may be a resistance marker. These HLA associations with disease indicate that development of TE in AIDS patients is affected by a gene or genes in the HLA complex and that HLA-DQ typing may help in decisions regarding TE prophylaxis.
引用
收藏
页码:265 / 268
页数:4
相关论文
共 15 条
[1]  
BROWN BW, 1977, STATISTICS BIOMEDICA, P231
[2]  
BROWN CR, 1990, J IMMUNOL, V145, P3438
[3]   DIFFERENCES IN HLA CLASS-II ALLELES OF ISOLATED SOUTH-AMERICAN INDIAN POPULATIONS FROM BRAZIL AND ARGENTINA [J].
CERNA, M ;
FALCO, M ;
FRIEDMAN, H ;
RAIMONDI, E ;
MACCAGNO, A ;
FERNANDEZVINA, M ;
STASTNY, P .
HUMAN IMMUNOLOGY, 1993, 37 (04) :213-220
[4]  
IMANISHI T, 1992, 11TH P INT HIST WORK, V1, P1065
[5]  
ITESCU S, 1992, J ACQ IMMUN DEF SYND, V5, P37
[6]  
JEANNET M, 1989, J ACQ IMMUN DEF SYND, V2, P28
[7]   ASSOCIATIONS BETWEEN HLA FREQUENCIES AND PATHOGENIC FEATURES OF HUMAN-IMMUNODEFICIENCY-VIRUS TYPE-1 INFECTION IN SEROCONVERTERS FROM THE AMSTERDAM-COHORT-OF-HOMOSEXUAL-MEN [J].
KLEIN, MR ;
KEET, IPM ;
DAMARO, J ;
BENDE, RJ ;
HEKMAN, A ;
MESMAN, B ;
KOOT, M ;
DEWAAL, LP ;
COUTINHO, RA ;
MIEDEMA, F .
JOURNAL OF INFECTIOUS DISEASES, 1994, 169 (06) :1244-1249
[8]   HLA-DQB1 AND HLA-DQA1 TYPING BY PCR AMPLIFICATION WITH SEQUENCE-SPECIFIC PRIMERS (PCR-SSP) IN 2 HOURS [J].
OLERUP, O ;
ALDENER, A ;
FOGDELL, A .
TISSUE ANTIGENS, 1993, 41 (03) :119-134
[9]   PROGRESSION TO AIDS IN FRENCH HEMOPHILIACS - ASSOCIATION WITH HLA-B35 [J].
SAHMOUD, T ;
LAURIAN, Y ;
GAZENGEL, C ;
SULTAN, Y ;
GAUTREAU, C ;
COSTAGLIOLA, D .
AIDS, 1993, 7 (04) :497-500
[10]  
Samuel, 1994, TXB AIDS MED, P223