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Bench-to-bedside review: Natural killer cells in sepsis - guilty or not guilty?

机译:从病床到病床回顾:败血症中的自然杀伤细胞-有罪还是无罪?

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摘要

Bacterial sepsis and septic shock are complex inflammatory disorders associated with a systemic inflammatory response syndrome. In the most severe cases of infection, an overzealous release of pro-inflammatory cytokines and inflammatory mediators by activated leukocytes, epithelial cells and endothelial cells, known as a 'cytokine storm', leads to deleterious effects such as organ dysfunction and even death. By the end of the 20th century, natural killer (NK) cells were for the first time identified as important players during sepsis. The role of this cell type was, however, double-edged, either 'angel' or 'devil' depending upon the bacterial infection model under study. Bacterial sensors (such as Toll-like receptors) have recently been shown to be expressed at the protein level in these cells. In addition, NK cells are important sources of interferon-γ and granulocyte-macrophage colony-stimulating factor, which are pro-inflammatory cytokines necessary to fight infection but can contribute to deleterious inflammation as well. Interestingly, an adaptative response occurs aimed to silence them, similar to the well-known phenomenon of endotoxin reprogramming.
机译:细菌性败血症和败血性休克是与全身性炎症反应综合征相关的复杂炎症疾病。在最严重的感染病例中,活化的白细胞,上皮细胞和内皮细胞过度释放促炎性细胞因子和炎性介质,被称为“细胞因子风暴”,导致有害作用,例如器官功能障碍,甚至死亡。到20世纪末,自然杀伤(NK)细胞首次被鉴定为败血症中的重要角色。然而,取决于正在研究的细菌感染模型,这种细胞类型的作用是双边缘的,即“天使”或“魔鬼”。最近显示细菌传感器(例如Toll样受体)在这些细胞中以蛋白质水平表达。另外,NK细胞是干扰素-γ和粒细胞-巨噬细胞集落刺激因子的重要来源,它们是抵抗感染所必需的促炎细胞因子,但也可能导致有害的炎症。有趣的是,发生了旨在使它们沉默的适应性反应,类似于众所周知的内毒素重编程现象。

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