4.7 Article

Host Determinants of HIV-1 Control in African Americans

Journal

JOURNAL OF INFECTIOUS DISEASES
Volume 201, Issue 8, Pages 1141-1149

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1086/651382

Keywords

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Funding

  1. National Institute of Allergy and Infectious Diseases [NIAID], National Institutes of Health [NIH] [Y1-AI5072, 5 T32 GM007754-29, AI067854]
  2. National Cancer Institute (NCI), NIH [HHSN261200800001E]
  3. National Heart, Lung, and Blood Institute [UO1-AI-35042, 5-M01-RR-00052, UO1-AI-35043, UO1-AI-37984, UO1-AI-35039, UO1-AI-35040, UO1-AI-37613, UO1-AI-35041]

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We performed a whole-genome association study of human immunodeficiency virus type 1 (HIV-1) set point among a cohort of African Americans (n = 515), and an intronic single-nucleotide polymorphism (SNP) in the HLA-B gene showed one of the strongest associations. We use a subset of patients to demonstrate that this SNP reflects the effect of the HLA-B*5703 allele, which shows a genome-wide statistically significant association with viral load set point (P = 5.6 x 10(-10)). These analyses therefore confirm a member of the HLA-B*57 group of alleles as the most important common variant that influences viral load variation in African Americans, which is consistent with what has been observed for individuals of European ancestry, among whom the most important common variant is HLA-B*5701.

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