生物
病毒学
病毒
干扰素
甲型流感病毒
抗病毒蛋白
埃博拉病毒
登革热病毒
跨膜蛋白
病毒复制
病毒包膜
冠状病毒
基因
核糖核酸
遗传学
疾病
2019年冠状病毒病(COVID-19)
医学
受体
病理
传染病(医学专业)
作者
Charles C. Bailey,Guocai Zhong,I‐Chueh Huang,Michael Farzan
出处
期刊:Annual Review of Virology
[Annual Reviews]
日期:2014-07-08
卷期号:1 (1): 261-283
被引量:418
标识
DOI:10.1146/annurev-virology-031413-085537
摘要
Animal cells use a wide variety of mechanisms to slow or prevent replication of viruses. These mechanisms are usually mediated by antiviral proteins whose expression and activities can be constitutive but are frequently amplified by interferon induction. Among these interferon-stimulated proteins, members of the IFITM (interferon-induced transmembrane) family are unique because they prevent infection before a virus can traverse the lipid bilayer of the cell. At least three human IFITM proteins-IFITM1, IFITM2, and IFITM3-have antiviral activities. These activities limit infection in cultured cells by many viruses, including dengue virus, Ebola virus, influenza A virus, severe acute respiratory syndrome coronavirus, and West Nile virus. Murine Ifitm3 controls influenza A virus infection in vivo, and polymorphisms in human IFITM3 correlate with the severity of both seasonal and highly pathogenic avian influenza virus. Here we review the discovery and characterization of the IFITM proteins, describe the spectrum of their antiviral activities, and discuss potential mechanisms underlying these effects.
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