Program in Innate Immunity, Division of Infectious Diseases and Immunology, Department of Medicine, University of Massachusetts Medical School, Worcester, MA, USA.
Innate Immunity Research Unit, GlaxoSmithKline, Collegeville, PA, USA.
Nat Rev Genet. 2019 Nov;20(11):657-674. doi: 10.1038/s41576-019-0151-1. Epub 2019 Jul 29.
The detection of pathogens through nucleic acid sensors is a defining principle of innate immunity. RNA-sensing and DNA-sensing receptors sample subcellular compartments for foreign nucleic acids and, upon recognition, trigger immune signalling pathways for host defence. Over the past decade, our understanding of how the recognition of nucleic acids is coupled to immune gene expression has advanced considerably, particularly for the DNA-sensing receptor cyclic GMP-AMP synthase (cGAS) and its downstream signalling effector stimulator of interferon genes (STING), as well as the molecular components and regulation of this pathway. Moreover, the ability of self-DNA to engage cGAS has emerged as an important mechanism fuelling the development of inflammation and implicating the cGAS-STING pathway in human inflammatory diseases and cancer. This detailed mechanistic and biological understanding is paving the way for the development and clinical application of pharmacological agonists and antagonists in the treatment of chronic inflammation and cancer.
通过核酸传感器检测病原体是先天免疫的一个决定性原则。RNA 感应和 DNA 感应受体对细胞内区室中的外来核酸进行采样,一旦识别,就会触发宿主防御的免疫信号通路。在过去的十年中,我们对核酸识别如何与免疫基因表达偶联的理解有了很大的进展,特别是对于 DNA 感应受体环鸟苷酸-腺苷酸合酶 (cGAS)及其下游信号效应物干扰素基因刺激物 (STING),以及该途径的分子成分和调节。此外,自身 DNA 与 cGAS 结合的能力已成为炎症发展的重要机制,并使 cGAS-STING 途径与人类炎症性疾病和癌症有关。这种详细的机制和生物学理解为开发和临床应用药理学激动剂和拮抗剂治疗慢性炎症和癌症铺平了道路。