生物
干扰素
TLR7型
细胞内寄生虫
免疫系统
Ⅰ型干扰素
微生物学
细胞内
模式识别受体
TLR9型
病毒感染
受体
单核细胞增生李斯特菌
先天免疫系统
病菌
免疫学
特里夫
病毒学
Toll样受体
病毒
细菌
细胞生物学
基因
基因表达
遗传学
DNA甲基化
作者
Andrea K. Perry,Gang Chen,Dahai Zheng,Hong Tang,Genhong Cheng
出处
期刊:Cell Research
[Springer Nature]
日期:2005-06-01
卷期号:15 (6): 407-422
被引量:360
标识
DOI:10.1038/sj.cr.7290309
摘要
Type I interferons (IFN) are well studied cytokines with anti-viral and immune-modulating functions. Type I IFNs are produced following viral infections, but until recently, the mechanisms of viral recognition leading to IFN production were largely unknown. Toll like receptors (TLRs) have emerged as key transducers of type I IFN during viral infections by recognizing various viral components. Furthermore, much progress has been made in defining the signaling pathways downstream of TLRs for type I IFN production. TLR7 and TLR9 have become apparent as universally important in inducing type I IFN during infection with most viruses, particularly by plasmacytoid dendritic cells. New intracellular viral pattern recognition receptors leading to type I IFN production have been identified. Many bacteria can also induce the up-regulation of these cytokines. Interestingly, recent studies have found a detrimental effect on host cells if type I IFN is produced during infection with the intracellular gram-positive bacterial pathogen, Listeria monocytogenes. This review will discuss the recent advances made in defining the signaling pathways leading to type I IFN production.
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