Departments of Obstetrics and Gynecology, Division of Maternal-Fetal Medicine, Baylor College of Medicine, Houston, TX; Departments of Obstetrics and Gynecology, Division of Maternal-Fetal Medicine, Texas Children's Hospital, Houston, TX.
Department of Pathology and Immunology, Baylor College of Medicine, Houston, TX; Department of Pathology and Immunology, Texas Children's Hospital, Houston, TX.
Am J Obstet Gynecol. 2017 Mar;216(3):209-225. doi: 10.1016/j.ajog.2017.01.020. Epub 2017 Jan 23.
Zika virus is an emerging mosquito-borne (Aedes genus) arbovirus of the Flaviviridae family. Following epidemics in Micronesia and French Polynesia during the past decade, more recent Zika virus infection outbreaks were first reported in South America as early as May 2013 and spread to now 50 countries throughout the Americas. Although no other flavivirus has previously been known to cause major fetal malformations following perinatal infection, reports of a causal link between Zika virus and microcephaly, brain and ocular malformations, and fetal loss emerged from hard-hit regions of Brazil by October 2015. Among the minority of infected women with symptoms, clinical manifestations of Zika virus infection may include fever, headache, arthralgia, myalgia, and maculopapular rash; however, only 1 of every 4-5 people who are infected have any symptoms. Thus, clinical symptom reporting is an ineffective screening tool for the relative risk assessment of Zika virus infection in the majority of patients. As previously occurred with other largely asymptomatic viral infections posing perinatal transmission risk (such as HIV or cytomegalovirus), we must develop and implement rapid, sensitive, and specific screening and diagnostic testing for both viral detection and estimation of timing of exposure. Unfortunately, despite an unprecedented surge in attempts to rapidly advance perinatal clinical testing for a previously obscure arbovirus, there are several ongoing hindrances to molecular- and sonographic-based screening and diagnosis of congenital Zika virus infection. These include the following: (1) difficulty in estimating the timing of exposure for women living in endemic areas and thus limited interpretability of immunoglobulin M serologies; (2) cross-reaction of immunoglobulin serologies with other endemic flaviruses, such as dengue; (3) persistent viremia and viruria in pregnancy weeks to months after primary exposure; and (4) fetal brain malformations and anomalies preceding the sonographic detection of microcephaly. In this commentary, we discuss screening and diagnostic considerations that are grounded not only in the realities of current obstetrical practice in a largely global population but also in basic immunology and virology. We review recent epidemiological data pertaining to the risk of congenital Zika virus malformations based on trimester of exposure and consider side by side with emerging data demonstrating replication of Zika virus in placental and fetal tissue throughout gestation. We discuss limitations to ultrasound based strategies that rely largely or solely on the detection of microcephaly and provide alternative neurosonographic approaches for the detection of malformations that may precede or occur independent of a small head circumference. This expert review provides information that is of value for the following: (1) obstetrician, maternal-fetal medicine specialist, midwife, patient, and family in cases of suspected Zika virus infection; (2) review of the methodology for laboratory testing to explore the presence of the virus and the immune response; (3) ultrasound-based assessment of the fetus suspected to be exposed to Zika virus with particular emphasis on the central nervous system; and (4) identification of areas ready for development.
Zika 病毒是黄病毒科的一种新兴蚊媒(Aedes 属)虫媒病毒。在过去十年中,密克罗尼西亚和法属波利尼西亚发生流行疫情之后,2013 年 5 月,南美洲首次报告了最近的 Zika 病毒感染疫情,并蔓延至目前美洲的 50 个国家。尽管此前没有其他黄病毒会导致围产期感染后出现严重的胎儿畸形,但到 2015 年 10 月,巴西受灾严重的地区出现了 Zika 病毒与小头畸形、脑和眼部畸形以及胎儿丢失之间存在因果关系的报告。在少数出现症状的受感染妇女中,Zika 病毒感染的临床表现可能包括发热、头痛、关节痛、肌痛和斑丘疹;然而,每 4-5 名感染者中只有 1 人有任何症状。因此,临床症状报告对于评估大多数患者的 Zika 病毒感染相对风险是一种无效的筛查工具。与以前存在围产期传播风险的其他大多数无症状病毒感染(如 HIV 或巨细胞病毒)一样,我们必须开发和实施快速、敏感和特异性的筛查和诊断检测,以检测病毒并估计暴露时间。不幸的是,尽管以前所未有的速度尝试对以前不为人知的虫媒病毒进行围产期临床检测,但在先天性 Zika 病毒感染的分子和超声筛查和诊断方面仍存在几个持续存在的障碍。这些包括以下几点:(1)对于生活在流行地区的妇女,难以估计暴露时间,因此免疫球蛋白 M 血清学的解释能力有限;(2)免疫球蛋白血清学与其他地方性黄病毒(如登革热)交叉反应;(3)在初次接触后数周到数月内,妊娠时仍持续存在病毒血症和病毒尿症;(4)胎儿脑畸形和异常先于超声检测到小头畸形。在本评论中,我们讨论了筛查和诊断的考虑因素,这些考虑因素不仅基于当前全球范围内大多数产科实践的现实,而且还基于基础免疫学和病毒学。我们回顾了最近关于基于暴露 trimester 的先天性 Zika 病毒畸形风险的流行病学数据,并与新兴数据并排考虑,这些数据显示 Zika 病毒在整个妊娠期间在胎盘和胎儿组织中复制。我们讨论了主要或完全依赖于小头畸形检测的超声策略的局限性,并提供了用于检测可能先于或独立于小头围出现的畸形的替代神经超声方法。本专家评论提供了以下方面有价值的信息:(1)疑似 Zika 病毒感染的产科医生、围产医学专家、助产士、患者和家属;(2)对存在病毒和免疫反应的实验室检测方法的回顾;(3)对疑似接触 Zika 病毒的胎儿进行基于超声的评估,特别强调中枢神经系统;(4)确定准备开发的领域。