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自然杀伤细胞在大鼠对细胞内细菌单核细胞增生李斯特菌的抗性中的作用。

The role of natural killer cells in resistance to the intracellular bacterium Listeria monocytogenes in rats.

作者信息

Shegarfi H, Sydnes K, Løvik M, Inngjerdingen M, Rolstad B, Naper C

机构信息

Department of Anatomy, Institute of Basic Medical Sciences, University of Oslo, Oslo, Norway.

出版信息

Scand J Immunol. 2009 Sep;70(3):238-44. doi: 10.1111/j.1365-3083.2009.02292.x.

Abstract

We have investigated the influence of early innate immune resistance mechanisms on infection with the intracellular bacterium Listeria monocytogenes in rats. Rats were injected i.v. with various amounts of Listeria and the number of bacterial colonies in the spleen was determined at different time points after infection. A bacterial dose as low as 2 x 10(4) cells gave reproducible infection within the spleen. Athymic nude rats lacking normal T cells but with a robust NK cell repertoire for MHC antigens were more resistant to bacterial replication within the spleen than were normal littermate rats and eliminated the infection within 3 days. In vivo depletion of NK cells, or NK subpopulations expressing Ly49 receptors, increased the bacterial load in the spleen, indicating that these cells were important in the initial control of Listeria infection. An increased frequency of Ly49 expressing NK cells in Listeria-infected rats further supported this notion. As several rat strains, unlike mice, display a large repertoire of MHC-recognizing activating Ly49 receptors, these observations raise the interesting possibility that NK cells may recognize alterations in the MHC-I molecules on Listeria-infected cells leading to their elimination before the adaptive immune system comes into play.

摘要

我们研究了早期先天性免疫抵抗机制对大鼠感染胞内细菌单核细胞增生李斯特菌的影响。给大鼠静脉注射不同数量的李斯特菌,并在感染后的不同时间点测定脾脏中的细菌菌落数。低至2×10⁴个细胞的细菌剂量就能在脾脏中引发可重复的感染。无胸腺裸鼠缺乏正常T细胞,但具有针对MHC抗原的强大NK细胞库,与正常同窝大鼠相比,它们对脾脏内细菌复制的抵抗力更强,并在3天内清除了感染。体内耗尽NK细胞或表达Ly49受体的NK亚群会增加脾脏中的细菌载量,表明这些细胞在李斯特菌感染的初始控制中很重要。李斯特菌感染的大鼠中表达Ly49的NK细胞频率增加进一步支持了这一观点。由于与小鼠不同,几种大鼠品系展示了大量识别MHC的激活型Ly49受体,这些观察结果提出了一个有趣的可能性,即NK细胞可能识别李斯特菌感染细胞上MHC-I分子的改变,从而在适应性免疫系统发挥作用之前将其清除。

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