Host determinants of HIV-1 control in African Americans.


Autoria(s): Pelak, K; Goldstein, DB; Walley, NM; Fellay, J; Ge, D; Shianna, KV; Gumbs, C; Gao, X; Maia, JM; Cronin, KD; Hussain, SK; Carrington, M; Michael, NL; Weintrob, AC; Infectious Disease Clinical Research Program HIV Working Group; National Institute of Allergy and Infectious Diseases Center for HIV/AIDS Vaccine Immunology (CHAVI)
Data(s)

15/04/2010

Formato

1141 - 1149

Identificador

http://www.ncbi.nlm.nih.gov/pubmed/20205591

J Infect Dis, 2010, 201 (8), pp. 1141 - 1149

http://hdl.handle.net/10161/4146

1537-6613

Idioma(s)

ENG

en_US

Relação

J Infect Dis

10.1086/651382

Journal of Infectious Diseases

Tipo

Journal Article

Cobertura

United States

Resumo

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.

Palavras-Chave #Adolescent #Adult #African Americans #DNA-Binding Proteins #Disease Progression #Genome-Wide Association Study #Genotype #HIV Infections #HIV-1 #HLA-B Antigens #HLA-C Antigens #Humans #Male #Middle Aged #Phenotype #Polymorphism, Single Nucleotide #Viral Load #Young Adult