TLR-9 (-1237)*T/C polymorphism in russian COVID-19 patients from the chelyabinsk region

S. Belyaeva, T. Suslova, Daria C. Stashkevich, Svetlana E. Balandina, Daria E. Mjakotina, Maria S. Milonchenko
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Abstract

In COVID-19, the clinical outcome depends on a wide range of factors, including genetic features. Among them, TLRs, the genes encoding the receptors of innate immune system are of particular interest since they play the key role in development of innate immune response. The present study concerns the newely identified allelic variants of the TLR-9 (-1237)*T/C gene in Russian residents from the Chelyabinsk Region who had COVID-19 complicated by the bilateral viral pneumonia. Polymorphic variants of TLR-9 (-1237)*T/ C were determined by polymerase chain reaction. It was found that, among the COVID-19 patients, a TLR-9 allele (-1237 C) with higher transcriptional activity was more common than in the control group (19.421% and 11.275%, respectively, p = 0.019), and its homozygous genotype TLR-9 (-1237)*C was not detected in the comparison group. TLR-9 allele (-1237)*T in the patients with COVID-19 was less common in comparison with the control group (80.579% and 88.725%, respectively, p = 0.019). Taking into account the differences in suggested TLR-9 expression in more severe COVID-19 patients, we compared distribution of TLR-9 (-1237)*T/ С allele polymorphism in the patients with different severity of COVID-19. In the group of patients with mild form, the TLR-9 (-1237)*T/T genotype was more common as compared with patients who had more severe clinical course. The differences were significant at the trend level when compared with patients with a medium-severity disease (86.364% and 66,000%, respectively; p = 0.076).
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俄罗斯车里雅宾斯克地区新冠肺炎患者TLR-9 (-1237)*T/C多态性
在COVID-19中,临床结果取决于多种因素,包括遗传特征。其中,tlr是编码先天免疫系统受体的基因,在先天免疫反应的发展中起着关键作用,因此受到特别关注。本研究涉及来自车里雅宾斯克地区的俄罗斯居民新发现的TLR-9 (-1237)*T/C基因等位变异,这些居民患有COVID-19合并双侧病毒性肺炎。采用聚合酶链反应检测TLR-9 (-1237)*T/ C多态性变异。结果发现,在COVID-19患者中,转录活性较高的TLR-9等位基因(-1237 C)比对照组更常见(分别为19.421%和11.275%,p = 0.019),对照组未检测到其纯合子基因型TLR-9 (-1237)*C。TLR-9等位基因(-1237)*T在新冠肺炎患者中的发生率低于对照组(分别为80.579%和88.725%,p = 0.019)。考虑重症患者TLR-9建议表达差异,比较不同重症患者TLR-9 (-1237)*T/ С等位基因多态性分布。在轻型患者组中,TLR-9 (-1237)*T/T基因型比临床病程较重的患者更常见。与中度疾病患者相比,在趋势水平上差异显著(分别为86.364%和660000%;P = 0.076)。
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