Association of the HLA-B*52 allele with non-progression to AIDS in Brazilian HIV-1-infected individuals

被引:21
作者
Teixeira, S. L. M. [1 ]
da Sa, N. B. R. [1 ]
Campos, D. P. [2 ]
Coelho, A. B. [2 ]
Guimaraes, M. L. [1 ]
Leite, T. C. N. F. [1 ]
Veloso, V. G. [2 ]
Morgado, M. G. [1 ]
机构
[1] Fiocruz MS, Inst Oswaldo Cruz, Lab AIDS & Mol Immunol, BR-21040360 Rio De Janeiro, Brazil
[2] Fiocruz MS, Evandro Chagas Clin Res Inst, BR-21040360 Rio De Janeiro, Brazil
关键词
LONG-TERM NONPROGRESSORS; T-CELL RESPONSES; HIV CONTROLLERS; CLASS-I; ELITE CONTROLLERS; IMMUNE-RESPONSES; VIRAL CONTROL; HLA-B; INFECTION; GENES;
D O I
10.1038/gene.2014.14
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Several human leukocyte antigen (HLA) class I alleles are associated with the susceptibility to human immunodeficiency virus-1 (HIV-1) infection and/or AIDS progression. Of these, the HLA-B alleles are considered the strongest genetic determinant of disease outcome. We evaluated the influence of the HLA-B alleles on AIDS progression among HIV-1-positive individuals from Rio de Janeiro, Brazil, who were categorized as rapid progressors (RPs), typical progressors (TPs) or long-term non-progressors (LTNPs). In this study, significant differences in HLA-B allele frequencies were observed among the three progression groups for the B*48, B*49 and B*52 alleles. After controlling for other factors associated with AIDS progression, the presence of the B*52 allele was shown to be a significant protective factor (hazard ratio (HR) 0.49 (95% confidence interval (Cl) 0.27-0.90) P<0.03). Although no direct association was observed between the presence of the B*27 or B*57 allele and the LTNP profile compared with the TP or RP groups, the adjusted model confirmed that these alleles are protective factors against AIDS progression (HR 0.62 (95% CI 0.38-0.99) P<0.05), as previously described. These data corroborate the existence of significant differences in HLA-B allele frequencies among the distinct AIDS progression profiles-and further elucidate the role of HLA alleles in the outcome of HIV infections in diverse populations.
引用
收藏
页码:256 / 262
页数:7
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