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Human Macrophages, but Not Dendritic Cells, Are Activated and Produce Alpha/Beta Interferons in Response to Mopeia Virus Infection

机译:人类巨噬细胞而不是树突状细胞被激活,并响应于pepeia病毒感染而产生α/β干扰素

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摘要

Lassa virus (LV) and Mopeia virus (MV) are closely related members of the Arenavirus genus, sharing 75% amino acid sequence identity. However, LV causes hemorrhagic fever in humans and nonhuman primates, whereas MV cannot induce disease. We have previously shown that antigen-presenting cells (APC)—macrophages (MP) and dendritic cells (DC)—sustain high replication rates of LV but are not activated, suggesting that they play a role in the immunosuppression observed in severe cases of Lassa fever. Here, we infected human APC with MV and analyzed the cellular responses induced. MV infection was productive in MP and even more so in DC. Apoptosis was not induced in either cell type. Moreover, unlike DC, MP were early and strongly activated in response to MV, as shown by the increased surface expression of CD86, CD80, CD54, CD40, and HLA-abc and by the production of mRNA encoding alpha interferon (IFN-α), IFN-β, tumor necrosis factor alpha and interleukin-6. In addition, MV-infected MP produced less of the virus than DC, which was related to the fact that these cells secreted IFN-α. Thus, the strong activation of MP is probably a major event in the control of MV infection and may be involved in the induction of an adaptive immune response in infected hosts. These results may explain the difference in pathogenicity between LV and MV.
机译:Lassa病毒(LV)和Mopeia病毒(MV)是Arenavirus属的密切相关成员,具有75%的氨基酸序列同一性。但是,LV会导致人类和非人类灵长类动物出血热,而MV无法诱发疾病。先前我们已经表明,抗原呈递细胞(APC)-巨噬细胞(MP)和树突状细胞(DC)-维持LV的高复制率,但未被激活,这表明它们在严重的Lassa病例中观察到的免疫抑制中起作用发热。在这里,我们用MV感染了人类APC,并分析了诱导的细胞反应。 MV感染在MP中产生作用,而在DC中则更为明显。两种细胞类型均未诱导凋亡。此外,与DC不同,MP响应MV而被早期激活并被强烈激活,这表现为CD86,CD80,CD54,CD40和HLA-abc的表面表达增加以及编码α干扰素(IFN-α)的mRNA产生。 ,IFN-β,肿瘤坏死因子α和白介素6。此外,感染MV的MP产生的病毒少于产生DC的病毒,这与这些细胞分泌IFN-α的事实有关。因此,MP的强激活可能是控制MV感染的主要事件,并且可能参与了感染宿主中适应性免疫应答的诱导。这些结果可以解释LV和MV之间的致病性差异。

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