Bailey Charles C, Zhong Guocai, Huang I-Chueh, Farzan Michael
Department of Infectious Diseases, The Scripps Research Institute, Jupiter, Florida 33458.
Department of Cell Biology and Neuroscience, College of Natural and Agricultural Sciences, University of California, Riverside, California 92521.
Annu Rev Virol. 2014 Nov 1;1:261-283. doi: 10.1146/annurev-virology-031413-085537.
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 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.
动物细胞利用多种机制来减缓或阻止病毒复制。这些机制通常由抗病毒蛋白介导,其表达和活性可以是组成性的,但常常通过干扰素诱导而增强。在这些干扰素刺激的蛋白中,IFITM(干扰素诱导跨膜蛋白)家族成员很独特,因为它们在病毒穿过细胞脂质双层之前就能阻止感染。至少三种人类IFITM蛋白——IFITM1、IFITM2和IFITM3——具有抗病毒活性。这些活性限制了许多病毒在培养细胞中的感染,包括登革病毒、埃博拉病毒、甲型流感病毒、严重急性呼吸综合征冠状病毒和西尼罗河病毒。小鼠Ifitm3在体内控制甲型流感病毒感染,人类中的多态性与季节性和高致病性禽流感病毒的严重程度相关。在这里,我们综述了IFITM蛋白的发现和特征,描述了它们抗病毒活性的范围,并讨论了这些效应潜在的机制。