HLA-DR and -DQ associations with melioidosis

被引:21
作者
Dharakul, T
Vejbaesya, S
Chaowagul, W
Luangtrakool, P
Stephens, HAF
Songsivilai, S
机构
[1] Mahidol Univ, Siriraj Hosp, Fac Med, Dept Immunol, Bangkok 10700, Thailand
[2] Mahidol Univ, Siriraj Hosp, Fac Med, Dept Transfus Med, Bangkok 10700, Thailand
[3] Sappasitprasong Gen Hosp, Dept Med, Ubonratchathani 34000, Thailand
关键词
D O I
10.1016/S0198-8859(98)00052-4
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Melioidosis is an important infectious disease of southeast Asia caused by an intracellular bacterium, Burkholderia pseudomallei. Cellular immunity is postulated to play important roles in immunity to melioidosis that may influence the severity and clinical outcome of the disease. The present study was undertaken to investigate possible associations of melioidosis with HLA class II alleles. HLA typing of HLA-DRB1, -DQA1, and -DQB1 was performed using polymerase chain reaction and sequence-specific oligonucleotide hybridization (PCR-SSO). Seventy-nine melioidosis patients and 105 healthy, ethnically and geographically matched controls mere studied. Among 24 DRB1 alleles, 7 DQA1 alleles, and 13 DQB1 alleles identified in this population, an association with melioidosis was observed with DRB1*1602 which was increased in melioidosis patients (10.1%) compared to normal controls (4.8%), p = 0.047 (odds ratio (OR) = 2.25). In addition, significant increase of DRB1*1602 allele frequency and decrease of DQA1*03 were also observed in septicemic melioidosis patients, the most severe form of the disease (p = 0.01, OR = 3.10; and p = 0.047, respectively). Furthermore, a trend of association of DRB1*0701, DQA1*0201, and DQB1*0201 with relapse cases of melioidosis was also noted. In contrast, no HLA association was observed in localized melioidosis or melioidosis with diabetes mellitus. These findings provide the suggestive evidence of an immunogenetic basis of certain aspects of melioidosis. (C) American Society for Histocompatibility and Immunogenetics, 1998. Published by Elsevier Science Inc.
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页码:580 / 586
页数:7
相关论文
共 15 条
[1]   HLA-A, -B, -DRB1, -DQA1, and -DQB1 polymorphism in Thais [J].
Chandanayingyong, D ;
Stephens, HAF ;
Klaythong, R ;
Sirikong, M ;
Udee, S ;
Longta, P ;
Chantangpol, R ;
Bejrachandra, S ;
Rungruang, E .
HUMAN IMMUNOLOGY, 1997, 53 (02) :174-182
[2]  
CHAOWAGUL W, 1993, J INFECT DIS, V168, P1181, DOI 10.1093/infdis/168.5.1181
[3]   MELIOIDOSIS - A MAJOR CAUSE OF COMMUNITY-ACQUIRED SEPTICEMIA IN NORTHEASTERN THAILAND [J].
CHAOWAGUL, W ;
WHITE, NJ ;
DANCE, DAB ;
WATTANAGOON, Y ;
NAIGOWIT, P ;
DAVIS, TME ;
LOOAREESUWAN, S ;
PITAKWATCHARA, N .
JOURNAL OF INFECTIOUS DISEASES, 1989, 159 (05) :890-899
[4]  
CHIEWSILP P, 1997, HLA GENETIC DIVERSIT, V2
[5]  
Dance D. A. B., 1990, Reviews in Medical Microbiology, V1, P143
[6]  
DANCE DAB, 1991, CLIN MICROBIOL REV, V4, P361
[7]   TUBERCULOSIS IN PATIENTS WITH VARIOUS HLA PHENOTYPES [J].
KHOMENKO, AG ;
LITVINOV, VI ;
CHUKANOVA, VP ;
POSPELOV, LE .
TUBERCLE, 1990, 71 (03) :187-192
[8]  
Kimura A, 1992, HLA 1991, V1, P397
[9]  
MEHRA NK, 1990, TROP MED PARASITOL, V41, P352
[10]   HOMOGENEITY OF LIPOPOLYSACCHARIDE ANTIGENS IN PSEUDOMONAS-PSEUDOMALLEI [J].
PITT, TL ;
AUCKEN, H ;
DANCE, DAB .
JOURNAL OF INFECTION, 1992, 25 (02) :139-&