Ishii Ken J, Akira Shizuo
Exploratory Research for Advanced Technology (ERATO), Japan Science and Technology Agency (JST) and Department of Host Defense, Research Institute for Microbial Diseases, Osaka University, 3-1 Yamada-oka, Suita, Osaka 565-0871, Japan.
Trends Immunol. 2006 Nov;27(11):525-32. doi: 10.1016/j.it.2006.09.002. Epub 2006 Sep 18.
DNA in microbes or host cells is normally sequestered from the immune system, and therefore inert, but becomes an active immunostimulatory molecule during infection or tissue damage. Recent evidence suggests that Toll-like receptor (TLR)9, currently the only known immune sensor for DNA, recognizes more diverse elements in its ligand than initially thought, and must cooperate with additional host factors to provoke an optimal innate immune response in the physiological environment. Moreover, the innate immune system possesses a TLR9-independent, as-yet-undefined intracellular recognition machinery of double-stranded DNA that induces type I interferons through distinct signaling pathways. TLR9-dependent and TLR9-independent immune recognition of DNA might play crucial roles in DNA-associated protective immunity and in pathological autoimmunity.
微生物或宿主细胞中的DNA通常与免疫系统隔离,因此呈惰性,但在感染或组织损伤期间会成为一种活跃的免疫刺激分子。最近的证据表明,Toll样受体(TLR)9是目前已知的唯一一种DNA免疫传感器,其在配体中识别的元素比最初认为的更多样化,并且必须与其他宿主因子协同作用,才能在生理环境中引发最佳的先天免疫反应。此外,先天免疫系统拥有一种不依赖TLR9的、尚未明确的双链DNA细胞内识别机制,该机制通过不同的信号通路诱导I型干扰素。DNA的TLR9依赖性和TLR9非依赖性免疫识别可能在与DNA相关的保护性免疫和病理性自身免疫中发挥关键作用。