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人类 ZNFX1 缺陷与多系统炎症和易感性病毒感染。

Multisystem inflammation and susceptibility to viral infections in human ZNFX1 deficiency.

机构信息

Division of Immunology and Children's Research Center, University Children's Hospital Zurich, Zurich, Switzerland.

Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, Mass.

出版信息

J Allergy Clin Immunol. 2021 Aug;148(2):381-393. doi: 10.1016/j.jaci.2021.03.045. Epub 2021 Apr 17.

Abstract

BACKGROUND

Recognition of viral nucleic acids is one of the primary triggers for a type I interferon-mediated antiviral immune response. Inborn errors of type I interferon immunity can be associated with increased inflammation and/or increased susceptibility to viral infections as a result of dysbalanced interferon production. NFX1-type zinc finger-containing 1 (ZNFX1) is an interferon-stimulated double-stranded RNA sensor that restricts the replication of RNA viruses in mice. The role of ZNFX1 in the human immune response is not known.

OBJECTIVE

We studied 15 patients from 8 families with an autosomal recessive immunodeficiency characterized by severe infections by both RNA and DNA viruses and virally triggered inflammatory episodes with hemophagocytic lymphohistiocytosis-like disease, early-onset seizures, and renal and lung disease.

METHODS

Whole exome sequencing was performed on 13 patients from 8 families. We investigated the transcriptome, posttranscriptional regulation of interferon-stimulated genes (ISGs) and predisposition to viral infections in primary cells from patients and controls stimulated with synthetic double-stranded nucleic acids.

RESULTS

Deleterious homozygous and compound heterozygous ZNFX1 variants were identified in all 13 patients. Stimulation of patient-derived primary cells with synthetic double-stranded nucleic acids was associated with a deregulated pattern of expression of ISGs and alterations in the half-life of the mRNA of ISGs and also associated with poorer clearance of viral infections by monocytes.

CONCLUSION

ZNFX1 is an important regulator of the response to double-stranded nucleic acids stimuli following viral infections. ZNFX1 deficiency predisposes to severe viral infections and a multisystem inflammatory disease.

摘要

背景

识别病毒核酸是 I 型干扰素介导的抗病毒免疫反应的主要触发因素之一。I 型干扰素免疫的先天缺陷可导致炎症增加和/或由于干扰素产生失衡而导致对病毒感染的易感性增加。NFX1 型锌指结构域包含 1 型(ZNFX1)是一种干扰素刺激的双链 RNA 传感器,可限制 RNA 病毒在小鼠中的复制。ZNFX1 在人类免疫反应中的作用尚不清楚。

目的

我们研究了 8 个家族的 15 名患者,这些患者具有常染色体隐性免疫缺陷,其特征是 RNA 和 DNA 病毒的严重感染以及病毒触发的炎症发作,表现为噬血细胞性淋巴组织细胞增生症样疾病、早发性癫痫发作以及肾脏和肺部疾病。

方法

对 8 个家族的 13 名患者进行全外显子组测序。我们研究了患者和对照的原代细胞中转录组、干扰素刺激基因(ISGs)的转录后调节以及对合成双链核酸刺激的病毒易感性。

结果

在所有 13 名患者中均发现了有害的纯合子和复合杂合 ZNFX1 变体。用合成双链核酸刺激患者来源的原代细胞与 ISG 的表达失调模式相关联,并且与 ISG 的 mRNA 半衰期改变以及单核细胞清除病毒感染的能力较差相关联。

结论

ZNFX1 是病毒感染后对双链核酸刺激的反应的重要调节剂。ZNFX1 缺陷易导致严重的病毒感染和多系统炎症性疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4ad0/8569286/7ec5eced4fd6/nihms-1749221-f0001.jpg

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