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新冠病毒肺炎患者中I型干扰素反应低下:干扰素反应可能是新冠病毒肺炎的一种潜在治疗方法。

Low type I interferon response in COVID-19 patients: Interferon response may be a potential treatment for COVID-19.

作者信息

Salman Ahmed Abdulwahid, Waheed Mohammed Hussein, Ali-Abdulsahib Akeel Abd, Atwan Zeenah Weheed

机构信息

PCR Laboratory, Public Health Department, Basrah Health Directorate, Basrah, Iraq.

Microbiology Laboratory, Basrah Educational Hospital, Basrah, Iraq.

出版信息

Biomed Rep. 2021 May;14(5):43. doi: 10.3892/br.2021.1419. Epub 2021 Mar 9.

Abstract

Interferons (IFN) are antiviral cytokines that mitigate the effects of invading viruses early on during the infection process. SARS-CoV and MERS induce weak IFN responses; hence, the clinical trials which included recombinant IFN accompanied with other antiviral drugs exhibited improved results in terms of shortening the duration of illness. The aim of the present study was to evaluate the type I IFN response in COVID-19 patients to determine whether it is sufficient to eliminate or reduce the severity of the infection, and whether it can be recommended as a potential therapy. Total RNA samples were converted to cDNA and used as templates to evaluate the gene expression levels of IFN regulatory factor (IRF)3 and IFN-β in COVID-19 patients or control. The results showed that IRF3 gene expression was upregulated ~250-fold compared with the negative samples. In contrast, IFN-β expression increased slightly in COVID-19 patients. Consistent with other coronaviruses, such as SARS-CoV and MERS, COVID-19 infection does not induce an efficient IFN response to reduce the severity of the virus. This may be attributed to an incomplete response of IRF3 in activating the IFN-β promoter in the infected patients. The results suggest IFN-β or α may be used as potential treatments.

摘要

干扰素(IFN)是一类抗病毒细胞因子,可在感染过程早期减轻入侵病毒的影响。严重急性呼吸综合征冠状病毒(SARS-CoV)和中东呼吸综合征冠状病毒(MERS)诱导的干扰素反应较弱;因此,包含重组干扰素及其他抗病毒药物的临床试验在缩短病程方面显示出更好的结果。本研究的目的是评估2019冠状病毒病(COVID-19)患者的I型干扰素反应,以确定其是否足以消除或降低感染的严重程度,以及是否可推荐将其作为一种潜在治疗方法。将COVID-19患者或对照的总RNA样本逆转录为cDNA,并用作模板来评估干扰素调节因子(IRF)3和干扰素-β(IFN-β)的基因表达水平。结果显示,与阴性样本相比,IRF3基因表达上调了约250倍。相比之下,COVID-19患者的IFN-β表达略有增加。与SARS-CoV和MERS等其他冠状病毒一致,COVID-19感染不会诱导有效的干扰素反应来减轻病毒的严重程度。这可能归因于感染患者中IRF3在激活IFN-β启动子方面的反应不完全。结果表明,IFN-β或α可能用作潜在的治疗方法。

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Interferon-α2b Treatment for COVID-19.干扰素-α2b 治疗 COVID-19。
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