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首页> 外文期刊>The Journal of Experomental Medicine >Respiratory influenza virus infection induces intestinal immune injury via microbiota-mediated Th17 cell–dependent inflammation
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Respiratory influenza virus infection induces intestinal immune injury via microbiota-mediated Th17 cell–dependent inflammation

机译:呼吸道流感病毒感染通过微生物群介导的Th17细胞依赖性炎症诱导肠道免疫损伤

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摘要

Influenza in humans is often accompanied by gastroenteritis-like symptoms such as diarrhea, but the underlying mechanism is not yet understood. We explored the occurrence of gastroenteritis-like symptoms using a mouse model of respiratory influenza infection. We found that respiratory influenza infection caused intestinal injury when lung injury occurred, which was not due to direct intestinal viral infection. Influenza infection altered the intestinal microbiota composition, which was mediated by IFN-γ produced by lung-derived CCR9+CD4+ T cells recruited into the small intestine. Th17 cells markedly increased in the small intestine after PR8 infection, and neutralizing IL-17A reduced intestinal injury. Moreover, antibiotic depletion of intestinal microbiota reduced IL-17A production and attenuated influenza-caused intestinal injury. Further study showed that the alteration of intestinal microbiota significantly stimulated IL-15 production from intestinal epithelial cells, which subsequently promoted Th17 cell polarization in the small intestine in situ. Thus, our findings provide new insights into an undescribed mechanism by which respiratory influenza infection causes intestinal disease.
机译:人的流感经常伴有类似肠胃炎的症状,例如腹泻,但其潜在机制尚不清楚。我们使用呼吸道流感感染的小鼠模型探索了胃肠炎样症状的发生。我们发现,呼吸道流感感染会在发生肺部损伤时引起肠道损伤,这不是直接肠道病毒感染引起的。流感感染改变了肠道菌群组成,这是由募集到小肠的肺源性CCR9 + CD4 + T细胞产生的IFN-γ介导的。在PR8感染后,小肠中的Th17细胞明显增加,而中和IL-17A可以减少肠损伤。此外,肠道微生物群的抗生素消耗减少了IL-17A的产生,并减轻了由流感引起的肠道损伤。进一步的研究表明,肠道菌群的改变显着刺激了肠道上皮细胞产生IL-15,从而促进了小肠内Th17细胞的极化。因此,我们的发现为呼吸道流行性感冒引起肠道疾病的未知机制提供了新见解。

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