Association of symptomatic acute human parvovirus B19 infection with human leukocyte antigen class I and II alleles

被引:35
作者
Kerr, JR
Mattey, DL
Thomson, W
Poulton, KV
Ollier, WER
机构
[1] Royal Brompton Hosp, Univ London Imperial Coll Sci Technol & Med, Natl Heart & Lung Inst, Dept Microbiol, London SW3 6NP, England
[2] Haywood Hosp, Staffordshire Rheumatol Ctr, Stoke On Trent ST6 7AG, Staffs, England
[3] Univ Manchester, Arthrit Res Campaign Epidemiol Unit, Manchester, Lancs, England
[4] Univ Manchester, Ctr Integrated Genom Med Res, Manchester, Lancs, England
[5] Cent Manchester Healthcare Trust, Transplantat Lab, Manchester, Lancs, England
关键词
D O I
10.1086/341947
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
To determine the effect of the major histocompatibility complex on the development of symptoms during acute human parvovirus B19 infection, we compared human leukocyte antigen (HLA) class I and II alleles in 36 patients with symptomatic acute B19 infection with those in 1 900 control subjects from northwestern England. The frequency of each of HLA-DRB1*01 (P = .016), DRB1*04 (P = .007), and DRB1*07 (P < .001) alleles was significantly higher in parvovirus B19 patients than in control subjects. In the parvovirus group, 63.9% carried the rheumatoid arthritis-associated shared epitope sequence, compared with 45% of control subjects (odds ratio [OR], 2.2; 95% confidence interval [CI], 0.97-4.8; P = .04), and carriage was associated with fatigue during the acute phase (OR, 4.2; 95% CI, 0.8-23.9; P = .047). All symptomatic parvovirus-associated HLA-DRB1 molecules carry a neutrally charged glutamine at position 10 and a positively charged lysine at position 12 of the first hypervariable region. HLA-B49 was associated with parvovirus infection independently of HLA-DRB1*01, DRB1*04, and DRB1*07.
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页码:447 / 452
页数:6
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