Interferons and viruses: an evolutionary arms race of molecular interactions

被引:307
作者
Hoffmann, Hans-Heinrich [1 ]
Schneider, William M. [1 ]
Rice, Charles M. [1 ]
机构
[1] Rockefeller Univ, Lab Virol & Infect Dis, New York, NY 10065 USA
基金
美国国家卫生研究院;
关键词
interferons; interferon subtype; innate immunity; viruses; viral antagonism; vaccine adjuvants; PLASMACYTOID DENDRITIC CELLS; PARAMYXOVIRUS V-PROTEINS; HEPATITIS-C-VIRUS; TYROSINE-PHOSPHORYLATED STAT1; ANTIVIRAL SIGNALING PROTEIN; INNATE IMMUNE RECOGNITION; ALPHA SUBTYPE RESPONSE; TOLL-LIKE RECEPTOR-3; I IFN RESPONSES; RIG-I;
D O I
10.1016/j.it.2015.01.004
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 half a century has passed since interferons (IFNs) were discovered and shown to inhibit virus infection in cultured cells. Since then, researchers have steadily brought to light the molecular details of IFN signaling, catalogued their pleiotropic effects on cells, and harnessed their therapeutic potential for a variety of maladies. While advances have been plentiful, several fundamental questions have yet to be answered and much complexity remains to be unraveled. We explore the current knowledge surrounding four main questions: are type I IFN subtypes differentially produced in response to distinct pathogens? How are IFN subtypes distinguished by cells? What are the mechanisms and consequences of viral antagonism? Lastly, how can the IFN response be harnessed to improve vaccine efficacy?
引用
收藏
页码:124 / 138
页数:15
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