Molecular and Cellular Therapeutics and RCSI Research Institute, Royal College of Surgeons in Ireland, 123 St. Stephens Green, Dublin 2, Ireland.
Molecular and Cellular Therapeutics and RCSI Research Institute, Royal College of Surgeons in Ireland, 123 St. Stephens Green, Dublin 2, Ireland.
Cytokine Growth Factor Rev. 2014 Dec;25(6):745-57. doi: 10.1016/j.cytogfr.2014.07.019. Epub 2014 Aug 15.
Innate immune detection and subsequent immune responses rely on the initial recognition of pathogen specific molecular motifs. Foreign nucleic acids are key structures recognised by the immune system, recognition of which occurs mainly through the use of nucleic acid receptors including members of the Toll-like receptors, AIM2-like receptors, RIG-I-like receptors and intracellular DNA receptors. While the immune system is critically important in protecting the host from infection, it is of utmost importance that it is tightly regulated, in order to prevent recognition of self-nucleic acids and the subsequent development of autoimmunity. Defects in the mechanisms regulating such pathways, for example mutations in endonucleases that clear DNA, altered expression of nucleic acid sensors and defects in negative regulators of these signalling pathways involved in RNA/DNA sensing, have all been implicated in promoting the generation of autoimmune responses. This evidence, as reviewed here, suggests that novel therapeutics targeting these sensors and their downstream pathways may be of use in the treatment of patients with autoimmune diseases such as systemic lupus erythematosus, rheumatoid arthritis and primary Sjögren's syndrome.
先天免疫检测和随后的免疫反应依赖于对病原体特异性分子模体的初始识别。外源核酸是免疫系统识别的关键结构,其识别主要通过使用核酸受体来实现,包括 Toll 样受体、AIM2 样受体、RIG-I 样受体和细胞内 DNA 受体的成员。虽然免疫系统对于保护宿主免受感染至关重要,但至关重要的是要对其进行严格调控,以防止识别自身核酸并随后发展为自身免疫。调控这些途径的机制缺陷,例如清除 DNA 的核酸内切酶的突变、核酸传感器的表达改变以及参与 RNA/DNA 感应的这些信号通路的负调节剂缺陷,都与促进自身免疫反应的产生有关。正如本文所综述的那样,这一证据表明,针对这些传感器及其下游途径的新型治疗方法可能有助于治疗自身免疫性疾病,如系统性红斑狼疮、类风湿关节炎和原发性干燥综合征。