Safari Mahnaz, Tavakoli Rezvan, Aghasadeghi Mohammadreza, Tabatabaee Bafroee Akram Sadat, Fateh Abolfazl, Rahimi Pooneh
Department of Biology, East Tehran Branch, Islamic Azad University, Tehran, Iran.
Department of Hepatitis and AIDS and Blood Transmitted Diseases, Pasteur Institute of Iran, Tehran, Iran.
Nucleosides Nucleotides Nucleic Acids. 2025;44(1):41-56. doi: 10.1080/15257770.2024.2344179. Epub 2024 Apr 25.
Understanding the complex mechanisms of the immune system in dealing with the COVID-19 infection, which is probably related to the polymorphism in cytokine and chemokine genes, can explain the pro-inflammatory condition of patients. Therefore, in this study, the relationship between the frequency of single nucleotide polymorphisms in the two pro-inflammatory genes dipeptidylpeptidase 9 (DPP9) and interferon alpha and beta receptor subunit 2 (IFNAR2) and the severity of COVID-19 was assessed. This study involved 954 COVID-19 patients, including 528 recovered and 426 deceased patients. To investigate the polymorphisms of rs2236757 and rs2109069, we used the polymerase chain reaction with the restriction fragment length polymorphism assay. The results showed that rs2236757 A allele is related to the reduced severity of the disease, whereas the incidence of rs2109069 A allele was higher among the deceased than recovered individuals. On the other hand, in people carrying the G allele in the gene polymorphism and the allele A in the gene polymorphism, the improvement of the disease was significantly higher. In conclusion, the results showed that rs2236757 A allele is related to the decrease in the severity of the disease, while the frequency of rs2109069 A allele was higher in deceased people than in recovered people. This shows the important role of genes related to inflammatory responses as well as the role of genetic variants of these genes in the severity of COVID-19.
了解免疫系统应对新冠病毒感染的复杂机制(这可能与细胞因子和趋化因子基因的多态性有关),可以解释患者的促炎状态。因此,在本研究中,评估了两种促炎基因二肽基肽酶9(DPP9)和干扰素α和β受体亚基2(IFNAR2)的单核苷酸多态性频率与新冠病毒疾病严重程度之间的关系。本研究纳入了954例新冠病毒患者,其中528例康复,426例死亡。为了研究rs2236757和rs2109069的多态性,我们使用了聚合酶链反应与限制性片段长度多态性分析。结果显示,rs2236757 A等位基因与疾病严重程度降低有关,而rs2109069 A等位基因在死亡患者中的发生率高于康复患者。另一方面,在基因多态性中携带G等位基因且在基因多态性中携带A等位基因的人群中,疾病改善情况显著更高。总之,结果表明rs2236757 A等位基因与疾病严重程度降低有关,而rs2109069 A等位基因在死亡人群中的频率高于康复人群。这显示了与炎症反应相关基因的重要作用以及这些基因的遗传变异在新冠病毒疾病严重程度中的作用。