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寨卡病毒相关小头畸形的新生儿表现出明显的全身炎症失衡。

Newborns With Zika Virus-Associated Microcephaly Exhibit Marked Systemic Inflammatory Imbalance.

机构信息

Instituto Gonçalo Moniz, Fundação Oswaldo Cruz, Salvador, Brazil.

Multinational Organization Network Sponsoring Translational and Epidemiological Research (MONSTER) Initiative, Salvador, Brazil.

出版信息

J Infect Dis. 2020 Jul 23;222(4):670-680. doi: 10.1093/infdis/jiaa197.

Abstract

BACKGROUND

Zika virus (ZIKV) is an emergent flavivirus initially considered a benign and self-limited exanthematic illness. In 2015, a new epidemic emerged in northeastern of Brazil with increased incidence of a previously rare clinical outcome, microcephaly, in newborns from mothers who were infected during pregnancy. Little is known about the immunopathogenesis of ZIKV-associated microcephaly. Understanding the inflammatory profile and degree of inflammation of persons affected with such condition is an important step towards development of innovative therapeutic strategies.

METHODS

A case-control study compared plasma levels of several inflammatory biomarkers from newborns with ZIKV microcephaly, asymptomatic ZKV infection, or uninfected controls. Plasma biomarkers were assessed using Luminex. A series of multidimensional analysis was performed to characterize the systemic immune activation profile of the clinical groups.

RESULTS

We identified an inflammatory signature associated with ZIKV microcephaly that suggested an increased inflammation. Network analysis suggested that ZIKV microcephaly is associated with imbalanced immune activation and inflammation. The cephalic perimeter was inversely proportional with the degree of inflammatory perturbation. Furthermore, a combination of plasma inflammatory biomarkers could discriminate ZIKV with microcephaly from those with ZIKV without microcephaly or uninfected neonates.

CONCLUSIONS

An intense inflammatory imbalance that is proportional to the disease severity hallmarks ZIKV microcephaly.

摘要

背景

寨卡病毒(ZIKV)是一种新兴的黄病毒,最初被认为是一种良性和自限性的出疹性疾病。2015 年,巴西东北部出现了一种新的疫情,孕妇感染寨卡病毒后,新生儿小头畸形的发病率上升,这是一种以前罕见的临床结局。人们对寨卡病毒相关小头畸形的免疫发病机制知之甚少。了解受感染者的炎症特征和炎症程度是开发创新治疗策略的重要步骤。

方法

一项病例对照研究比较了寨卡病毒小头畸形、无症状寨卡病毒感染或未感染对照新生儿的血浆中几种炎症生物标志物的水平。使用 Luminex 评估血浆生物标志物。进行了一系列多维分析,以描述临床组的系统免疫激活特征。

结果

我们确定了与寨卡病毒小头畸形相关的炎症特征,表明炎症增加。网络分析表明,寨卡病毒小头畸形与免疫激活和炎症失衡有关。头围与炎症扰动的程度成反比。此外,血浆炎症生物标志物的组合可区分寨卡病毒伴小头畸形与寨卡病毒不伴小头畸形或未感染新生儿。

结论

与疾病严重程度成正比的强烈炎症失衡标志着寨卡病毒小头畸形。

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