Association of Toll-like receptor polymorphisms with HIV status in North Americans

被引:18
作者
Willie, B. [1 ]
Hall, N. B. [2 ]
Stein, C. M. [2 ,3 ]
Jurevic, R. J. [4 ]
Weinberg, A. [4 ]
Mehlotra, R. K. [1 ]
Zimmerman, P. A. [1 ]
机构
[1] Case Western Reserve Univ, Sch Med, Ctr Global Hlth & Dis, Cleveland, OH 44106 USA
[2] Case Western Reserve Univ, Dept Epidemiol & Biostat, Cleveland, OH 44106 USA
[3] Case Western Reserve Univ, Sch Med, Ctr Prote & Bioinformat, Cleveland, OH 44106 USA
[4] Case Western Reserve Univ, Sch Med, Dept Biol Sci, Cleveland, OH 44106 USA
基金
美国国家卫生研究院;
关键词
SINGLE-NUCLEOTIDE POLYMORPHISMS; HUMAN-IMMUNODEFICIENCY-VIRUS; SEQUENCE VARIANTS; BLOOD-DONORS; RECENT INSIGHTS; RESIDUAL RISK; IL-6; LEVELS; VIRAL LOAD; SUSCEPTIBILITY; PREVALENCE;
D O I
10.1038/gene.2014.54
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Single-nucleotide polymorphisms (SNPs) in Toll-like receptor (TLR) genes TLR2-4 and TLR7-9, but not in TLR1 and TLR6, have been previously evaluated regarding human immunodeficiency virus (HIV) acquisition and disease progression in various populations, most of which were European. In this study, we examined associations between a total of 41 SNPs in 8 TLR genes (TLR1-4, TLR6-9) and HIV status in North American subjects (total n = 276 (Caucasian, n = 102; African American, n = 150; other, n = 24)). Stratification of the data by self-identified race revealed that a total of nine SNPs in TLR1, TLR4, TLR6 and TLR8 in Caucasians, and two other SNPs, one each in TLR4 and TLR8, in African Americans were significantly associated with HIV status at P < 0.05. Concordant with the odds ratios of these SNPs, significant differences were observed in the SNP allele frequencies between HIV+ and HIV - subjects. Finally, in Caucasians, certain haplotypes of single (TLR1 and TLR4) and heterodimer (TLR2_TLR6) genes may be inferred as 'susceptible' or 'protective'. Our study provides in-depth insight into the associations between TLR variants, particularly TLR1 and TLR6, and HIV status in North Americans, and suggests that these associations may be race specific.
引用
收藏
页码:569 / 577
页数:9
相关论文
共 88 条
[1]  
[Anonymous], PHARM GENOMICS ADMIX
[2]   TLR4 mutations are associated with endotoxin hyporesponsiveness in humans [J].
Arbour, NC ;
Lorenz, E ;
Schutte, BC ;
Zabner, J ;
Kline, JN ;
Jones, M ;
Frees, K ;
Watt, JL ;
Schwartz, DA .
NATURE GENETICS, 2000, 25 (02) :187-+
[3]   Genetic analysis of HNF4A polymorphisms in Caucasian-American type 2 diabetes [J].
Bagwell, AM ;
Bento, JL ;
Mychaleckyj, JC ;
Freedman, BI ;
Langefeld, CD ;
Bowden, DW .
DIABETES, 2005, 54 (04) :1185-1190
[4]   Toll-like receptor variants are associated with infant HIV-1 acquisition and peak plasma HIV-1 RNA level [J].
Beima-Sofie, Kristin M. ;
Bigham, Abigail W. ;
Lingappa, Jairam R. ;
Wamalwa, Dalton ;
Mackelprang, Romel D. ;
Bamshad, Michael J. ;
Maleche-Obimbo, Elizabeth ;
Richardson, Barbra A. ;
John-Stewart, Grace C. .
AIDS, 2013, 27 (15) :2431-2439
[5]   Functional Characterization of Naturally Occurring Genetic Variants in the Human TLR1-2-6 Gene Family [J].
Ben-Ali, Meriem ;
Corre, Beatrice ;
Manry, Jeremy ;
Barreiro, Luis B. ;
Quach, Helene ;
Boniotto, Michele ;
Pellegrini, Sandra ;
Quintana-Murci, Lluis .
HUMAN MUTATION, 2011, 32 (06) :643-652
[6]   Intracellular Toll-like Receptors [J].
Blasius, Amanda L. ;
Beutler, Bruce .
IMMUNITY, 2010, 32 (03) :305-315
[7]   Polymorphisms in Toll-like receptor 9 influence the clinical course of HIV-1 infection [J].
Bochud, Pierre-Yves ;
Hersberger, Martin ;
Taffe, Patrick ;
Bochud, Murielle ;
Stein, Catherine M. ;
Rodrigues, Stephanie D. ;
Calandra, Thierry ;
Francioli, Patrick ;
Telenti, Amalio ;
Speck, Roberto F. ;
Aderem, Alan .
AIDS, 2007, 21 (04) :441-446
[8]  
BREEN EC, 1990, J IMMUNOL, V144, P480
[9]   Recent insights into the structure of Toll-like receptors and post-translational modifications of their associated signalling proteins [J].
Carpenter, Susan ;
O'Neill, Luke A. J. .
BIOCHEMICAL JOURNAL, 2009, 422 :1-10
[10]   Recent insights into the role of Toll-like receptors in viral infection [J].
Carty, M. ;
Bowie, A. G. .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2010, 161 (03) :397-406