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Ⅰ型干扰素的诱导在感染 Whipple 病细菌,即屈螺酮体(Tropheryma whipplei)期间是有害的。

Type I interferon induction is detrimental during infection with the Whipple's disease bacterium, Tropheryma whipplei.

机构信息

Université de la Méditerranée, Centre National de la Recherche Scientifique, Unité Mixte de Recherche 6236, Marseille, France.

出版信息

PLoS Pathog. 2010 Jan 15;6(1):e1000722. doi: 10.1371/journal.ppat.1000722.

Abstract

Macrophages are the first line of defense against pathogens. Upon infection macrophages usually produce high levels of proinflammatory mediators. However, macrophages can undergo an alternate polarization leading to a permissive state. In assessing global macrophage responses to the bacterial agent of Whipple's disease, Tropheryma whipplei, we found that T. whipplei induced M2 macrophage polarization which was compatible with bacterial replication. Surprisingly, this M2 polarization of infected macrophages was associated with apoptosis induction and a functional type I interferon (IFN) response, through IRF3 activation and STAT1 phosphorylation. Using macrophages from mice deficient for the type I IFN receptor, we found that this type I IFN response was required for T. whipplei-induced macrophage apoptosis in a JNK-dependent manner and was associated with the intracellular replication of T. whipplei independently of JNK. This study underscores the role of macrophage polarization in host responses and highlights the detrimental role of type I IFN during T. whipplei infection.

摘要

巨噬细胞是抵御病原体的第一道防线。感染后,巨噬细胞通常会产生高水平的促炎介质。然而,巨噬细胞可以发生另一种极化,导致允许状态。在评估巨噬细胞对 Whipple 病细菌病原体 Whipple 氏疏螺旋体的全球反应时,我们发现 T. whipplei 诱导了与细菌复制兼容的 M2 巨噬细胞极化。令人惊讶的是,感染巨噬细胞的这种 M2 极化与凋亡诱导和功能性 I 型干扰素(IFN)反应有关,通过 IRF3 激活和 STAT1 磷酸化。使用缺乏 I 型 IFN 受体的小鼠巨噬细胞,我们发现这种 I 型 IFN 反应是 T. whipplei 诱导的巨噬细胞凋亡所必需的,并且与 JNK 独立于 JNK 相关,并与 T. whipplei 的细胞内复制有关。这项研究强调了巨噬细胞极化在宿主反应中的作用,并突出了 I 型 IFN 在 T. whipplei 感染期间的有害作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a3a/2798751/4f5b48d66dd4/ppat.1000722.g001.jpg

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