TLR-2 gene Arg753Gln polymorphism is strongly associated with acute rheumatic fever in children

被引:100
作者
Berdeli, A [1 ]
Celik, HA
Özyürek, R
Dogrusoz, B
Aydin, HH
机构
[1] Ege Univ, Sch Med, Dept Pediat, Mol Med Lab, TR-35100 Izmir, Turkey
[2] Ege Univ, Sch Med, Dept Biochem, TR-35100 Izmir, Turkey
[3] Ege Univ, Sch Med, Dept Pediat Cardiol, TR-35100 Izmir, Turkey
来源
JOURNAL OF MOLECULAR MEDICINE-JMM | 2005年 / 83卷 / 07期
关键词
acute rheumatic fever; TLR-2; gene polymorphism; single nucleotide polymorphism; infections;
D O I
10.1007/s00109-005-0677-x
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The recently described family of toll-like receptors (TLRs) is a key player in host immunity by mediating inflammatory reactions against a wide range of pathogens. Mutations and polymorphisms in TLRs have revealed the importance of TLRs in human defence against diseases. TLR-2 is reported to interact with different bacterial structures, including lipoproteins, peptidoglycan and lipoteichoic acid. To assess the role of TLR-2 gene polymorphism in acute rheumatic fever (ARF) etiopathology, 61 independent Caucasian Turkish patients and 91 child and 116 adult controls were studied. Antistreptolycin O, C-reactive protein, sedimentation and white blood cell counts were studied to evaluate the clinical characteristics of the patients. Genomic DNA was extracted from peripheral blood using a standard column extraction technique. The Arg753Gln and Arg677Trp polymorphisms were genotyped by polymerase chain reaction (PCR) restriction fragment length polymorphism. The PCR products for the TLR-2 gene were analysed on 1.5% agarose gel pre-stained with ethidium bromide. Compared with healthy adult controls, the Arg753Arg genotype was significantly decreased in the entire group of ARF cases [odds ratio (OR) 0.01, 95% confidence interval (95% CI) 0.0034-0.031, p < 0.0001]. Significantly, ARF patients were just 16 times more frequent with Gln allele (OR 15.6, 95% CI 7.87-30.8, p < 0.0001). Moreover, evidence for an intensifying effect of the Gln allele was noteworthy when patients with Arg753Gln genotype were compared with healthy controls (OR 97.1, 95% CI 32.5-290, p < 0.0001). However, no Arg677Trp polymorphism was detected in either patients or controls. Our data suggest that there is strong evidence for the biological role of TLR-2 in ARF. The common TLR-2 Arg to Gln polymorphism at position 753 significantly contributes to the pathogenesis of ARF. These results will allow the construction of a profile of individuals prone to ARF and may assist in developing new therapies.
引用
收藏
页码:535 / 541
页数:7
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