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白细胞介素-10缺陷小鼠表达γ干扰素信使核糖核酸,并且比正常的C57BL/6小鼠更快地从肾脏清除问号钩端螺旋体。

Il-10 deficient mice express IFN-γ mRNA and clear Leptospira interrogans from their kidneys more rapidly than normal C57BL/6 mice.

作者信息

Devlin Amy A, Halvorsen Priya J, Miller Jennifer C, Laster Scott M

机构信息

Reynolds American, Inc. 401 N. Main St., Winston Salem, NC 27101, United States.

Immunity, Inflammation and Disease Laboratory, Division of Intramural Research, National Institute of Environmental Health Sciences, NIH, Research Triangle Park, NC, United States.

出版信息

Immunobiology. 2017 May;222(5):768-777. doi: 10.1016/j.imbio.2017.02.004. Epub 2017 Feb 10.

Abstract

Leptospira interrogans (L. interrogans), the causative agent of leptospirosis, is a widespread zoonotic spirochete that lives a dual lifestyle. L. interrogans infects mice, rats, and wildlife in a persistent and asymptomatic fashion, while also causing productive and acute infections in other mammals such as humans and hamsters. Infections in humans can be fatal, accompanied by a cytokine storm and shock-like symptoms. Production of IL-10 has been noted in both rodent and human infections which has led a number of investigators to hypothesize that IL-10 plays a role in the pathogenesis of this disease. To test this hypothesis we have compared bacteremia and the cytokine response of normal and IL-10 deficient C57Bl/6 mice following ip infection with L. interrogans. In normal mice bacterial 16s mRNA was detected in both lung and kidney tissues within a day after infection. Levels of 16s mRNA then dropped in both organs with complete elimination from the lung by day 3 but persistence in the kidney for 7days after infection. In contrast, in IL-10 deficient mice, the organism was eliminated more rapidly from the kidney. We found that infection of both control and IL-10 deficient mice produced similar levels of a number of pro-inflammatory cytokine mRNAs. On the other hand, IFN-γ mRNA was only induced in IL-10 deficient mice. These results support the hypothesis that L. interrogans ability to induce IL-10, which in turn prevents production of IFN-γ and inhibits T cell immunity, may contribute to the persistent growth of this microorganism in the murine kidney.

摘要

问号钩端螺旋体(L. interrogans)是钩端螺旋体病的病原体,是一种广泛存在的人畜共患螺旋体,具有双重生活方式。问号钩端螺旋体以持续且无症状的方式感染小鼠、大鼠和野生动物,同时也会在其他哺乳动物(如人类和仓鼠)中引发有菌血症的急性感染。人类感染可能是致命的,伴有细胞因子风暴和类似休克的症状。在啮齿动物和人类感染中均已发现白细胞介素-10(IL-10)的产生,这使得许多研究人员推测IL-10在这种疾病的发病机制中起作用。为了验证这一假设,我们比较了正常和IL-10缺陷型C57Bl/6小鼠经腹腔感染问号钩端螺旋体后的菌血症和细胞因子反应。在正常小鼠中,感染后一天内肺和肾组织中均可检测到细菌16s mRNA。然后,两个器官中的16s mRNA水平均下降,到第3天时肺中完全清除,但感染后7天肾中仍持续存在。相比之下,在IL-10缺陷型小鼠中,病原体从肾脏中清除得更快。我们发现,对照小鼠和IL-10缺陷型小鼠感染后产生的多种促炎细胞因子mRNA水平相似。另一方面,γ干扰素(IFN-γ)mRNA仅在IL-10缺陷型小鼠中被诱导。这些结果支持了以下假设:问号钩端螺旋体诱导IL-10的能力,进而阻止IFN-γ的产生并抑制T细胞免疫,可能有助于这种微生物在小鼠肾脏中的持续生长。

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