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首页> 外文期刊>PLoS Pathogens >TGF?2-activation by dendritic cells drives Th17 induction and intestinal contractility and augments the expulsion of the parasite Trichinella spiralis in mice
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TGF?2-activation by dendritic cells drives Th17 induction and intestinal contractility and augments the expulsion of the parasite Trichinella spiralis in mice

机译:树突状细胞对TGFβ2的激活驱动Th17诱导和肠道收缩,并增加了寄生虫旋毛虫的驱逐

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Helminths are highly prevalent metazoan parasites that infect over a billion of the world’s population. Hosts have evolved numerous mechanisms to drive the expulsion of these parasites via Th2-driven immunity, but these responses must be tightly controlled to prevent equally devastating immunopathology. However, mechanisms that regulate this balance are still unclear. Here we show that the vigorous Th2 immune response driven by the small intestinal helminth Trichinella spiralis, is associated with increased TGFβ signalling responses in CD4+ T-cells. Mechanistically, enhanced TGFβ signalling in CD4+ T-cells is dependent on dendritic cell-mediated TGFβ activation which requires expression of the integrin αvβ8. Importantly, mice lacking integrin αvβ8 on DCs had a delayed ability to expel a T. spiralis infection, indicating an important functional role for integrin αvβ8-mediated TGFβ activation in promoting parasite expulsion. In addition to maintaining regulatory T-cell responses, the CD4+ T-cell signalling of this pleiotropic cytokine induces a Th17 response which is crucial in promoting the intestinal muscle hypercontractility that drives worm expulsion. Collectively, these results provide novel insights into intestinal helminth expulsion beyond that of classical Th2 driven immunity, and highlight the importance of IL-17 in intestinal contraction which may aid therapeutics to numerous diseases of the intestine.
机译:蠕虫是高度流行的后生寄生虫,感染了全球十亿人口。宿主已经进化出许多机制来通过Th2驱动的免疫力驱赶这些寄生虫,但是必须严格控制这些反应,以防止同样具有破坏性的免疫病理学。但是,调节这种平衡的机制仍不清楚。在这里,我们显示由小肠蠕虫旋毛虫驱动的强烈Th2免疫应答与CD4 + T细胞中TGFβ信号传导应答增加有关。从机理上讲,CD4 + T细胞中增强的TGFβ信号传导依赖于树突状细胞介导的TGFβ激活,这需要表达整联蛋白αvβ8。重要的是,在DC上缺乏整合素αvβ8的小鼠驱逐螺旋螺旋体感染的能力有所延迟,这表明整合素αvβ8介导的TGFβ激活在促进寄生虫驱逐方面具有重要的功能作用。除了维持调节性T细胞反应外,该多效细胞因子的CD4 + T细胞信号转导还引起Th17反应,这对促进肠道肌肉过度收缩驱动蠕虫驱逐至关重要。总的来说,这些结果提供了对肠蠕虫驱除的超越常规Th2驱动的免疫力的新颖见解,并突显了IL-17在肠收缩中的重要性,这可能有助于治疗多种肠道疾病。

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