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细胞质 DNA 先天免疫途径。

Cytoplasmic DNA innate immune pathways.

机构信息

Department of Cell Biology and Sylvester Comprehensive Cancer Center, University of Miami Miller School of Medicine, Miami, FL 33136, USA.

出版信息

Immunol Rev. 2011 Sep;243(1):99-108. doi: 10.1111/j.1600-065X.2011.01051.x.

DOI:10.1111/j.1600-065X.2011.01051.x
PMID:21884170
Abstract

The innate immune system is responsible for detecting microbial invasion of the cell and for stimulating host defense countermeasures. These anti-pathogen procedures include the transcriptional activation of powerful antiviral genes such as the type I interferons (IFNs) or the triggering of inflammatory responses through interleukin-1 (IL-1) production. Over the past decade, key cellular sensors responsible for triggering innate immune signaling pathways and host defense have started to be resolved and include the Toll-like receptor (TLR), RIG-I-like helicase, and the cytoplasmic nucleotide-binding oligermerization domain-like receptor families. These sensors recognize non-self pathogen-associated molecular patterns such as microbial lipopolysaccharides and nucleic acids. For example, TLR9 has evolved to detect CpG DNA commonly found in bacteria and viruses and to initiate the production of IFN and other cytokines. In contrast, AIM2 (absent in melanoma 2) has been shown to be essential for mediating inflammatory responses involving IL-1β following the sensing of microbial DNA. Recently, a molecule referred to as STING (stimulator of IFN genes) was demonstrated as being vital for recognizing cytoplasmic DNA and for activating the production of innate immune genes in response to a variety of DNA pathogens and even certain RNA viruses. Comprehending the mechanisms of intracellular DNA-mediated innate immune signaling may lead to the design of new adjuvant concepts that will facilitate vaccine development and may provide important information into the origins of autoimmune disease.

摘要

先天免疫系统负责检测细胞内的微生物入侵,并刺激宿主防御措施。这些抗病原体程序包括转录激活强大的抗病毒基因,如 I 型干扰素(IFN),或通过白细胞介素-1(IL-1)产生引发炎症反应。在过去的十年中,负责触发先天免疫信号通路和宿主防御的关键细胞传感器开始得到解决,包括 Toll 样受体(TLR)、RIG-I 样螺旋酶和细胞质核苷酸结合寡聚化域样受体家族。这些传感器识别非自身病原体相关分子模式,如微生物脂多糖和核酸。例如,TLR9 已进化为检测细菌和病毒中常见的 CpG DNA,并启动 IFN 和其他细胞因子的产生。相比之下,AIM2(无黑色素瘤 2)已被证明对于在感知微生物 DNA 后介导涉及 IL-1β 的炎症反应至关重要。最近,一种称为 STING(干扰素基因刺激物)的分子被证明对于识别细胞质 DNA 以及激活对各种 DNA 病原体甚至某些 RNA 病毒的先天免疫基因的产生至关重要。理解细胞内 DNA 介导的先天免疫信号转导的机制可能会导致设计新的佐剂概念,这将有助于疫苗的开发,并为自身免疫疾病的起源提供重要信息。

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