Variation in the TLR10/TLR1/TLR6 locus is the major genetic determinant of interindividual difference in TLR1/2-mediated responses

被引:52
|
作者
Mikacenic, C. [1 ]
Reiner, A. P. [2 ]
Holden, T. D.
Nickerson, D. A. [3 ]
Wurfel, M. M.
机构
[1] Univ Washington, Harborview Med Ctr, Div Pulm & Crit Care Med, Dept Med, Seattle, WA 98104 USA
[2] Univ Washington, Dept Epidemiol, Seattle, WA 98104 USA
[3] Univ Washington, Dept Genome Sci, Seattle, WA 98104 USA
关键词
TLR; polymorphism; genomics; innate immunity; TOLL-LIKE RECEPTOR-2; KAPPA-B ACTIVATION; PROSTATE-CANCER; CUTTING EDGE; CLUSTER TLR10-TLR1-TLR6; MICROBIAL LIPOPROTEINS; BACTERIAL LIPOPROTEINS; INFECTION; DISEASE; INNATE;
D O I
10.1038/gene.2012.53
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Toll-like receptor (TLR)-mediated innate immune responses are important in early host defense. Using a candidate gene approach, we previously identified genetic variation within TLR1 that is associated with hyper-responsiveness to a TLR1/2 agonist in vitro and with death and organ dysfunction in patients with sepsis. Here we report a genome-wide association study (GWAS) designed to identify genetic loci controlling whole blood cytokine responses to the TLR1/2 lipopeptide agonist, Pam(3)CSK(4) (N-palmitoyl-S-dipalmitoylglyceryl Cys-Ser-(Lys)(4)) ex vivo. We identified a very strong association (P < 1 x 10(-27)) between genetic variation within the TLR10/1/6 locus on chromosome 4, and Pam(3)CSK(4)-induced cytokine responses. This was the predominant association explaining over 35% of the population variance for this phenotype. Notably, strong associations were observed within TLR10, suggesting that genetic variation in TLR10 may influence bacterial lipoprotein-induced responses. These findings establish the TLR10/1/6 locus as the dominant common genetic factor controlling interindividual variability in Pam(3)CSK(4)-induced whole blood responses in the healthy population. Genes and Immunity (2013) 14, 52-57; doi: 10.1038/gene.2012.53; published online 15 November 2012
引用
收藏
页码:52 / 57
页数:6
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