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针对普马拉野鼠型汉坦病毒,NKG2C NK 细胞反应的剖析。

Dissection of the NKG2C NK cell response against Puumala Orthohantavirus.

机构信息

Center for Virology, Medical University of Vienna, Vienna, Austria.

出版信息

PLoS Negl Trop Dis. 2021 Dec 6;15(12):e0010006. doi: 10.1371/journal.pntd.0010006. eCollection 2021 Dec.

Abstract

BACKGROUND

Infections with the Puumala orthohantavirus (PUUV) in humans may cause hemorrhagic fever with renal syndrome (HFRS), known as nephropathia epidemica (NE), which is associated with acute renal failure in severe cases. In response to PUUV-infections, a subset of potent antiviral NKG2C+ NK cells expand, whose role in virus defence and pathogenesis of NE is unclear. NKG2C+ NK cell proliferation is mediated by binding of NKG2C/CD94 to HLA-E on infected cells. The proliferation and activation of NKG2C+ NK cells via the NKG2C/HLA-E axis is affected by different NKG2C (NKG2Cwt/del) and HLA-E (HLA-E*0101/0103) alleles, which naturally occur in the human host. Homozygous (NKG2Cdel/del) and heterozygous (NKG2Cwt/del) deletions of the NKG2C receptor results in an impaired NKG2C/CD94 mediated proliferation and activation of NKG2C+ cells. We therefore analyzed the PUUV-mediated NKG2C+ NK cell responses and the impact of different NKG2C and HLA-E alleles in NE patients.

METHODOLOGY/PRINCIPAL FINDINGS: NKG2C+ NK cell expansion and effector functions in PUUV-infected cells were investigated using flow cytometry and it was shown that PUUV-infected endothelial cells led to a NKG2C/CD94 mediated NKG2C+ NK cell activation and expansion, dependent on the HLA-G-mediated upregulation of HLA-E. Furthermore, the NKG2Cdel and HLA-E*0101/0103 alleles were determined in 130 NE patients and 130 matched controls, and it was shown that in NE patients the NKG2Cwt/del allele was significantly overrepresented, compared to the NKG2Cwt/wt variant (p = 0.01). In addition, in vitro analysis revealed that NKG2Cwt/del NK cells exhibited on overall a lower proliferation (p = 0.002) and lower IFNγ expression (p = 0.004) than NKG2Cwt/wt NK cells.

CONCLUSIONS/SIGNIFICANCE: Our results corroborate the substantial impact of the NKG2C/HLA-E axis on PUUV-specific NK cell responses. A weak NKG2C+ NK cell response, as reflected by NKG2Cwt/del variant, may be associated with a higher risk for a severe hantavirus infections.

摘要

背景

人类感染普马拉 orthohantavirus(PUUV)可能会导致肾综合征出血热(HFRS),又称流行性肾病(NE),在严重情况下会导致急性肾衰竭。针对 PUUV 感染,一部分有效的抗病毒 NKG2C+NK 细胞会扩增,但其在病毒防御和 NE 发病机制中的作用尚不清楚。NKG2C+NK 细胞的增殖是通过 NKG2C/CD94 与受感染细胞上的 HLA-E 结合介导的。NKG2C/HLA-E 轴通过 NKG2C 对 NKG2C+NK 细胞的增殖和激活的影响受不同的 NKG2C(NKG2Cwt/del)和 HLA-E(HLA-E*0101/0103)等位基因的影响,这些等位基因在人类宿主中自然存在。NKG2C 受体的纯合子(NKG2Cdel/del)和杂合子(NKG2Cwt/del)缺失导致 NKG2C/CD94 介导的 NKG2C+细胞增殖和激活受损。因此,我们分析了 PUUV 介导的 NKG2C+NK 细胞反应以及不同 NKG2C 和 HLA-E 等位基因在 NE 患者中的影响。

方法/主要发现:使用流式细胞术研究了 PUUV 感染细胞中的 NKG2C+NK 细胞扩增和效应功能,结果表明,PUUV 感染的内皮细胞导致 NKG2C/CD94 介导的 NKG2C+NK 细胞激活和扩增,这依赖于 HLA-G 介导的 HLA-E 上调。此外,在 130 名 NE 患者和 130 名匹配对照中确定了 NKG2Cdel 和 HLA-E*0101/0103 等位基因,结果表明与 NKG2Cwt/wt 变体相比,NE 患者中 NKG2Cwt/del 等位基因明显过多(p=0.01)。此外,体外分析显示,NKG2Cwt/del NK 细胞的增殖(p=0.002)和 IFNγ 表达(p=0.004)总体上低于 NKG2Cwt/wt NK 细胞。

结论/意义:我们的研究结果证实了 NKG2C/HLA-E 轴对 PUUV 特异性 NK 细胞反应的重要影响。较弱的 NKG2C+NK 细胞反应,如 NKG2Cwt/del 变体所示,可能与汉坦病毒感染的严重程度较高相关。

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