The broad-spectrum antiviral functions of IFIT and IFITM proteins

被引:673
作者
Diamond, Michael S. [1 ,2 ,3 ]
Farzan, Michael [4 ,5 ]
机构
[1] Washington Univ, Sch Med, Dept Med, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Mol Microbiol, St Louis, MO 63110 USA
[3] Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO 63110 USA
[4] Harvard Univ, New England Primate Res Ctr, Sch Med, Southborough, MA 01772 USA
[5] Harvard Univ, Dept Microbiol & Immunol, Sch Med, Southborough, MA 01772 USA
基金
美国国家卫生研究院;
关键词
INTERFERON-STIMULATED GENES; INDUCIBLE TRANSMEMBRANE PROTEINS; VIRUS-RNA REPLICATION; DOUBLE-STRANDED-RNA; WEST NILE VIRUS; MESSENGER-RNA; TRANSLATION INITIATION; S-PALMITOYLATION; DNA-REPLICATION; VIRAL-INFECTION;
D O I
10.1038/nri3344
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Over the past few years, several groups have identified new genes that are transcriptionally induced downstream of type I interferon (IFN) signalling and that inhibit infection by individual or multiple families of viruses. Among these IFN-stimulated genes with antiviral activity are two genetically and functionally distinct families - the IFN-induced protein with tetratricopeptide repeats (IFIT) family and the IFN-induced transmembrane protein (IFITM) family. This Review focuses on recent advances in identifying the unique mechanisms of action of IFIT and IFITM proteins, which explain their broad-spectrum activity against the replication, spread and pathogenesis of a range of human viruses.
引用
收藏
页码:46 / 57
页数:12
相关论文
共 82 条
[1]   Where, in antiviral defense, does IFIT1 fit? [J].
Ablasser, Andrea ;
Hornung, Veit .
NATURE IMMUNOLOGY, 2011, 12 (07) :588-590
[2]   Ifitm3 Limits the Severity of Acute Influenza in Mice [J].
Bailey, Charles C. ;
Huang, I-Chueh ;
Kam, Christina ;
Farzan, Michael .
PLOS PATHOGENS, 2012, 8 (09)
[3]   Global and distinct targets of IRF-5 and IRF-7 during innate response to viral infection [J].
Barnes, BJ ;
Richards, J ;
Mancl, M ;
Hanash, S ;
Beretta, L ;
Pitha, PM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (43) :45194-45207
[4]   Forced IFIT-2 expression represses LPS induced TNF-alpha expression at posttranscriptional levels [J].
Berchtold, Susanne ;
Manncke, Birgit ;
Klenk, Juliane ;
Geisel, Julia ;
Autenrieth, Ingo B. ;
Bohn, Erwin .
BMC IMMUNOLOGY, 2008, 9 (1)
[5]   STRUCTURE, CHROMOSOME LOCALIZATION, AND REGULATION OF EXPRESSION OF THE INTERFERON-REGULATED MOUSE IFI54/IFI56 GENE FAMILY [J].
BLUYSSEN, HAR ;
VLIETSTRA, RJ ;
FABER, PW ;
SMIT, EME ;
HAGEMEIJER, A ;
TRAPMAN, J .
GENOMICS, 1994, 24 (01) :137-148
[6]  
BRADBURY LE, 1993, J IMMUNOL, V151, P2915
[7]   The IFITM Proteins Mediate Cellular Resistance to Influenza A H1N1 Virus, West Nile Virus, and Dengue Virus [J].
Brass, Abraham L. ;
Huang, I-Chueh ;
Benita, Yair ;
John, Sinu P. ;
Krishnan, Manoj N. ;
Feeley, Eric M. ;
Ryan, Bethany J. ;
Weyer, Jessica L. ;
van der Weyden, Louise ;
Fikrig, Erol ;
Adams, David J. ;
Xavier, Ramnik J. ;
Farzan, Michael ;
Elledge, Stephen J. .
CELL, 2009, 139 (07) :1243-1254
[8]   IFITM Proteins Restrict Antibody-Dependent Enhancement of Dengue Virus Infection [J].
Chan, Ying Kai ;
Huang, I-Chueh ;
Farzan, Michael .
PLOS ONE, 2012, 7 (03)
[9]   TPR proteins: the versatile helix [J].
D'Andrea, LD ;
Regan, L .
TRENDS IN BIOCHEMICAL SCIENCES, 2003, 28 (12) :655-662
[10]   Cell-specific IRF-3 responses protect against West Nile virus infection by interferon-dependent and -independent mechanisms [J].
Daffis, Stephane ;
Samuel, Melanie A. ;
Keller, Brian C. ;
Gale, Michael, Jr. ;
Diamond, Michael S. .
PLOS PATHOGENS, 2007, 3 (07) :1005-1015