寨卡病毒感染的神经病理学。

Journal of neuroinfectious diseases Pub Date : 2016-06-01 Epub Date: 2016-06-23 DOI:10.4172/2314-7326.1000220
Isaac H Solomon, Danny A Milner, Rebecca D Folkerth
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摘要

寨卡病毒(ZIKV)是黄病毒科的一员,在2015年巴西疫情爆发之前,只与轻度疾病有关。在此期间,报告的小头症和格林-巴利综合征病例急剧增加,促使人们对寨卡病毒及其嗜神经特性可能存在的关联进行了重大研究。神经祖细胞和类器官的感染已被证明会诱导细胞凋亡和生长失调,小鼠研究已证明病毒在成人脑组织中复制,以及垂直传播导致胚胎大脑异常。已开始发表大量关于先天性寨卡病毒感染的临床和放射学发现的病例系列;然而,病理报告仅限于两个病例报告和两个小病例系列。到目前为止,这些发现主要局限于大脑,包括弥漫性灰质和白质受累,包括营养不良钙化、胶质细胞增生、小胶质细胞结节、噬神经细胞和分散的淋巴细胞。在一些病例中,胎盘组织出现轻度慢性绒毛炎,其余器官基本未受累。需要进行更大规模的系统研究,包括将组织学结果与母体感染时的胎龄进行相关性研究,以确定寨卡病毒引起的所有异常情况,并帮助指导未来的临床决策。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Neuropathology of Zika Virus Infection.

Zika virus (ZIKV) is a member of the Flaviviridae family that had been associated only with mild disease prior to the 2015 outbreak in Brazil. A dramatic increase in reported cases of microcephaly and Guillain-Barré syndrome during this time prompted significant research into possible associations with ZIKV and its neurotropic properties. Infection of neural progenitor cells and organoids have been shown to induce apoptosis and dysregulation of growth, and mouse studies have demonstrated viral replication in brain tissue in adults, as well as vertical transmission resulting in embryonic brain abnormalities. Large case series of clinical and radiological findings of congenital ZIKV infection have begun to be published; however, pathology reports have been limited to two case reports and two small case series. Thus far, the findings have largely been restricted to the brain and include diffuse grey and white matter involvement consisting of dystrophic calcifications, gliosis, microglial nodules, neuronophagia, and scattered lymphocytes. Mild chronic villitis was observed in the placental tissue in some cases, and the remaining organs were essentially uninvolved. Larger, systematic studies, including correlation of histological findings with gestational age at the time of maternal infection, will be required to determine the full range of Zika virus-induced abnormalities and to help guide future clinical decision making.

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