首页> 外文期刊>International journal of immunopathology and pharmacology. >TNFR1 mRNA Expression Level and TNFR1 Gene Polymorphisms are Predictive Markers for Susceptibility to Develop Invasive Pulmonary Aspergillosis
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TNFR1 mRNA Expression Level and TNFR1 Gene Polymorphisms are Predictive Markers for Susceptibility to Develop Invasive Pulmonary Aspergillosis

机译:TNFR1 mRNA表达水平和TNFR1基因多态性是发展为侵袭性肺曲霉病易感性的预测标记。

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Tumour necrosis factor (TNF) is primarily secreted by monocytes/macrophages and activated T lymphocytes in response to fungal infections. TNF acts through TNF receptor 1 (TNFR1) triggering a pro-inflammatory response, and therefore plays a pivotal role in immune regulation and host immune responses. We hypothesized that single nucleotide polymorphisms (SNPs) in TNFR1 gene may influence the innate immune response against Aspergillus. Three SNPs were genotyped in 275 individuals (144 immunocompromised haematological patients with high-risk of developing IPA and 131 healthy controls): TNFR1-383(A/C) (rs2234649) and TNFR1-609(G/T) (rs4149570) in the 5′ UTR region, and TNFR1+36(A/G) SNP (rs767455) in the first exon of the gene. Of the 144 haematological patients, 77 patients developed Invasive Pulmonary Aspergillosis (IPA) infection and the remaining 67 patients were not infected. TNFR1+36(A/G) and TNFR1-609(G/T) were associated with IPA susceptibility (p=0.033 and p=0.018, respectively). A role of TNFR1 genetic variants in the susceptibility of patients to develop IPA was also supported by the significantly lower TNFR1 mRNA expression level in IPA than in IPA-resistant patients and the strong correlation between the TNFR1-609 genetic variant and the expression levels of TNFR1. There was also a tendency for a higher frequency of galactomannan (GM) positivity in patients with TNFR1-609G/G genotype than in patients with TNFR1-609G/T (p=0.0909) or TNFR1-609T/T (p=0.0913) genotype. Predictive sequence analysis of the effects of TNFR1-609 promoter polymorphism revealed that this SNP might play a critical role in modifying the affinity of ICSBP/IRF-8, a transcription factor that is involved in the TNFR1-mediated activation of NFκB signalling pathway. Taken together, these data suggest that TNFR1 polymorphisms influence the risk of IPA disease and might be useful for risk stratification strategies. These findings need to be confirmed in validation studies with larger samples of haematological patients.
机译:肿瘤坏死因子(TNF)主要由单核细胞/巨噬细胞和活化的T淋巴细胞分泌,以响应真菌感染。 TNF通过TNF受体1(TNFR1)触发促炎反应,因此在免疫调节和宿主免疫反应中起着关键作用。我们假设TNFR1基因中的单核苷酸多态性(SNPs)可能会影响针对曲霉的先天免疫应答。在275名个体(144名免疫受损的血液学高危IPA病患者和131名健康对照)的3个SNP基因型中:TNFR1 -383(A / C)(rs2234649)和TNFR1 -609 (G / T)(rs4149570)位于5'UTR区,而TNFR1 +36(A / G) SNP(rs767455)位于该基因的第一个外显子。在144例血液学患者中,有77例发生了侵袭性肺曲霉病(IPA)感染,其余67例未感染。 TNFR1 +36(A / G)和TNFR1 -609(G / T)与IPA敏感性相关(分别为p = 0.033和p = 0.018)。 TNFR1遗传变异在IPA患者易感性中的作用也得到了支持,因为IPA的TNFR1 mRNA表达水平明显低于IPA耐药患者,而且TNFR1 -609 遗传之间的相关性很强变体和TNFR1的表达水平。基因型TNFR1 -609G / G 患者的半乳甘露聚糖(GM)阳性率也高于TNFR1 -609G / T 患者(p = 0.0909)或TNFR1 -609T / T (p = 0.0913)基因型。对TNFR1 -609 启动子多态性影响的预测序列分析表明,该SNP可能在修饰ICSBP / IRF-8的亲和力中起关键作用,ICSBP / IRF-8是TNFR1介导的转录因子激活NFκB信号通路。综上,这些数据表明TNFR1多态性影响IPA疾病的风险,可能对风险分层策略有用。这些发现需要在更多血液病患者样本的验证研究中得到证实。

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