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《2020年十大重大发现》中对《I型干扰素缺乏可导致严重新冠肺炎》的一篇评论

A commentary of "Type I interferon deficiency can lead to severe COVID-19" in 10 remarkable discoveries from 2020 in .

作者信息

Fang Xiangming

机构信息

Department of Anesthesiology, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.

出版信息

Fundam Res. 2022 Jan 30;2(2):351-352. doi: 10.1016/j.fmre.2022.01.005. eCollection 2022 Mar.

Abstract

In two articles published in online in September 2020, Zhang et al. [1] and Bastard et al. [2] elucidated a key factor in the progression to severe COVID-19; namely, a deficiency in interferon, especially type I interferon (IFN I). This deficiency might be caused by diverse reasons such as genetic mutations of genes encoding key antiviral signaling molecules, or the 'neutralization' of IFN I by endogenous antibodies. How does IFN I deficiency cause severe, life-threatening COVID-19? The most straightforward explanation is that such deficiency allows uncontrolled virus replication and spread. IFN I deficiency may also have other impacts on immune system function. Individuals with mutations in the IFN-I-induced signaling pathways may benefit from interferon therapies. In addition, individuals with neutralizing antibodies against IFN-α and IFN-ω may also benefit from other types of interferons provided in the therapy, such as IFN-β and IFN-λ.

摘要

在2020年9月在线发表的两篇文章中,张等人[1]和巴斯塔德等人[2]阐明了COVID-19进展为重症的一个关键因素,即干扰素缺乏,尤其是I型干扰素(IFN I)缺乏。这种缺乏可能由多种原因引起,如编码关键抗病毒信号分子的基因突变,或内源性抗体对IFN I的“中和”。IFN I缺乏如何导致严重的、危及生命的COVID-19?最直接的解释是这种缺乏会导致病毒不受控制地复制和传播。IFN I缺乏也可能对免疫系统功能产生其他影响。IFN-I诱导信号通路发生突变的个体可能从干扰素治疗中受益。此外,针对IFN-α和IFN-ω具有中和抗体的个体也可能从治疗中提供的其他类型干扰素(如IFN-β和IFN-λ)中受益。

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