首页> 外文期刊>Annals of the Rheumatic Diseases: A Journal of Clinical Rheumatology and Connective Tissue Research >A functional polymorphism of TIR-domain-containing adaptor protein is not associated with axial spondyloarthritis.
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A functional polymorphism of TIR-domain-containing adaptor protein is not associated with axial spondyloarthritis.

机译:含有TIR域的衔接子蛋白的功能多态性与轴向性脊椎关节炎无关。

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OBJECTIVE: A genetic variant of the toll-like receptor (TLR)2/4 adaptor protein TIRAP (single nucleotide polymorphism (SNP) C539T) was identified in a UK and in several African populations. The heterozygous genotype of this SNP has been associated with protection from severe infections. This allele results in an attenuated response to bacterial pathogens. As an exaggerated innate immune response to pathogens has been implicated in spondyloarthritis (SpA) pathogenesis, we analysed if the heterozygous C/T genotype was underrepresented in axial SpA compared with healthy controls. METHODS: 204 patients with axial SpA and 175 population-matched controls were included. SNP C539T was determined with a sequence-specific polymerase chain reaction and direct sequencing. RESULTS: The frequency of the haplotypes was similar in cases and controls (87% for C and 13% for T in both groups). The C/T genotype, which attenuates TLR signalling, was not underrepresented in cases versus controls (19% in controls vs 24% in cases, p = 0.44). The T/T genotype, was slightly lower in cases than in controls, although this was not significant (3.4% in controls vs 1% in cases, p = 0.15). Within the cases, there were no differences in disease phenotype or activity between patients with the C/C or C/T genotype. CONCLUSIONS: This study did not show significant associations of SNP S180L of the TLR2/4 adaptor protein TIRAP with axial SpA.
机译:目的:在英国和一些非洲人群中鉴定出了Toll样受体(TLR)2/4衔接蛋白TIRAP(单核苷酸多态性(SNP)C539T)的遗传变异。该SNP的杂合基因型与防止严重感染相关。该等位基因导致对细菌病原体的应答减弱。由于已经对脊椎关节炎(SpA)发病机制涉及了对病原体的先天免疫反应,因此我们分析了轴向SpA中杂合C / T基因型与健康对照相比是否代表不足。方法:纳入204例轴向SpA患者和175例人群匹配对照。 SNP C539T通过序列特异性聚合酶链反应和直接测序确定。结果:在病例和对照中,单倍型的频率相似(两组中C为87%,T为13%)。 C / T基因型减弱了TLR信号传导,在病例组和对照组中的比例并不低(对照组为19%,病例为24%,p = 0.44)。 T / T基因型在病例中比对照组略低,尽管并不显着(对照组为3.4%,病例为1%,p = 0.15)。在这些病例中,具有C / C或C / T基因型的患者在疾病表型或活动方面无差异。结论:本研究未显示TLR2 / 4衔接子蛋白TIRAP的SNP S180L与轴向SpA显着相关。

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