Functional assessment of Toll-like receptor 2 and its relevance in patients with Staphylococcus aureus infection of joint prosthesis

被引:15
作者
El-Helou, Odette [1 ]
Berbari, Elie F. [1 ]
Brown, Robert A. [1 ]
Gralewski, Jonathon H. [1 ]
Osmon, Douglas R. [1 ]
Razonable, Raymund R. [1 ]
机构
[1] Mayo Clin, Coll Med, Div Infect Dis, Rochester, MN 55905 USA
关键词
Prosthetic joint infection; Staphylococcus aureus; Toll-like receptors; Gene polymorphisms; Cytokines; INNATE IMMUNE-SYSTEM; CUTTING EDGE; PEPTIDOGLYCAN; RECOGNITION; POLYMORPHISMS; TLR2; ACTIVATION; ASSOCIATION; DISEASE; SECRETION;
D O I
10.1016/j.humimm.2010.10.001
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Staphylococcus aureus induces inflammation in experimental models through Toll-like receptor 2 (TLR2). The clinical relevance of this observation is debated. We evaluated the relationship between TLR2 R753Q single nucleotide polymorphism (SNP) and S aureus infection of joint prosthesis. Human embryonic kidney 293 (HEK293) cells transfected with wild-type and mutant R753Q TLR2 gene were assessed for response to S aureus peptidoglycan. Real-time polymerase chain reaction and gene sequencing of DNA were performed to assess TLR2 R753Q SNP in 76 patients with S aureus prosthetic joint infection (PJI) and 208 noninfected controls. HEK293 cells expressing wild-type TLR2 gene responded robustly to S aureus peptidoglycan, while cells with mutant R753Q TLR2 gene did not. The prevalence of R753Q SNP was high in S aureus PJI patients (heterozygous in 8%, and homozygous in 22%), although not significantly different from controls (12% and 27%, respectively). The TLR2 variant allele was not significantly associated with the risk or survival free of recurrent PJI S aureus. In conclusion, TLR2 R753QSNP disabled the cellular response to S aureus peptidoglycan in vitro. However, TLR2 R753Q SNP was not significantly associated with the risk or outcome of PJI due to S aureus in human patients. (c) 2011 American Society for Histocompatibility and Immunogenetics. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:47 / 53
页数:7
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