Viral evasion of DNA-stimulated innate immune responses

被引:57
作者
Christensen, Maria H. [1 ,2 ]
Paludan, Soren R. [1 ,2 ]
机构
[1] Aarhus Univ, Dept Biomed, Wilhelm Meyers Alle 4, DK-8000 Aarhus, Denmark
[2] Aarhus Univ, Aarhus Res Ctr Innate Immunol, DK-8000 Aarhus, Denmark
基金
英国医学研究理事会;
关键词
DNA sensing; evasion; innate immunology; STING; CYCLIC GMP-AMP; HUMAN CYTOMEGALOVIRUS; ADAPTER PROTEIN; DENDRITIC CELLS; RNADNA HYBRIDS; HOST-DEFENSE; SENSOR CGAS; IFI16; RECOGNITION; INFECTION;
D O I
10.1038/cmi.2016.06
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Cellular sensing of virus-derived nucleic acids is essential for early defenses against virus infections. In recent years, the discovery of DNA sensing proteins, including cyclic GMP-AMP synthase (cGAS) and gamma-interferon-inducible protein (IFI16), has led to understanding of how cells evoke strong innate immune responses against incoming pathogens carrying DNA genomes. The signaling stimulated by DNA sensors depends on the adaptor protein STING (stimulator of interferon genes), to enable expression of antiviral proteins, including type I interferon. To facilitate efficient infections, viruses have evolved a wide range of evasion strategies, targeting host DNA sensors, adaptor proteins and transcription factors. In this review, the current literature on virus-induced activation of the STING pathway is presented and we discuss recently identified viral evasion mechanisms targeting different steps in this antiviral pathway.
引用
收藏
页码:4 / 13
页数:10
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