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Perinatal analyses of Zika- and dengue virus-specific neutralizing antibodies: A microcephaly case-control study in an area of high dengue endemicity in Brazil

机译:寨卡病毒和登革热病毒特异性中和抗体的围产期分析:巴西高登革热流行地区的小头畸形病例对照研究

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摘要

Laboratory confirmation of Zika virus (ZIKV) infection during pregnancy is challenging due to cross-reactivity with dengue virus (DENV) and limited knowledge about the kinetics of anti-Zika antibody responses during pregnancy. We described ZIKV and DENV serological markers and the maternal-fetal transfer of antibodies among mothers and neonates after the ZIKV microcephaly outbreak in Northeast Brazil (2016). We included 89 microcephaly cases and 173 neonate controls at time of birth and their mothers. Microcephaly cases were defined as newborns with a particular head circumference (2 SD below the mean). Two controls without microcephaly were matched by the expected date of delivery and area of residence. We tested maternal serum for recent (ZIKV genome, IgM and IgG3 anti-NS1) and previous (ZIKV and DENV neutralizing antibodies [NAbs]) markers of infection. Multiple markers of recent or previous ZIKV and DENV infection in mothers were analyzed using principal component analysis (PCA). At delivery, 5.6% of microcephaly case mothers and 1.7% of control mothers were positive for ZIKV IgM. Positivity for ZIKV IgG3 anti-NS1 was 8.0% for case mothers and 3.5% for control mothers. ZIKV NAbs was slightly higher among mothers of cases (69.6%) than that of mothers of controls (57.2%; p = 0.054). DENV exposure was detected in 85.8% of all mothers. PCA discriminated two distinct components related to recent or previous ZIKV infection and DENV exposure. ZIKV NAbs were higher in newborns than in their corresponding mothers (p<0.001). We detected a high frequency of ZIKV exposure among mothers after the first wave of the ZIKV outbreak in Northeast Brazil. However, we found low sensitivity of the serological markers to recent infection (IgM and IgG3 anti-NS1) in perinatal samples of mothers of microcephaly cases. Since the neutralization test cannot precisely determine the time of infection, testing for ZIKV immune status should be performed as early as possible and throughout pregnancy to monitor acute Zika infection in endemic areas.
机译:由于与登革热病毒(DENV)的交叉反应以及对怀孕期间抗Zika抗体反应动力学的了解有限,因此在怀孕期间实验室确认Zika病毒(ZIKV)感染具有挑战性。我们描述了ZIKV和DENV血清学标志物以及在巴西东北部(2016)ZIKV小头症暴发后母婴之间抗体的母胎转移。我们纳入了89例小头畸形病例和173例出生时及其母亲的新生儿对照。小头畸形的病例定义为头围特定的新生儿(均值以下2 SD)。将两个无小头畸形的对照与预期的分娩日期和居住面积相匹配。我们测试了母体血清中感染的最新标记(ZIKV基因组,IgM和IgG3抗NS1)和先前的标记(ZIKV和DENV中和抗体[NAbs])。使用主成分分析(PCA)分析了母亲最近或以前感染ZIKV和DENV的多个标记。分娩时,5.6%的小头畸形母亲和1.7%的对照母亲ZIKV IgM呈阳性。 ZIKV IgG3抗NS1阳性的病例母亲为8.0%,对照母亲为3.5%。病例母亲中的ZIKV NAbs略高(69.6%),高于对照组母亲中的ZIKV NAbs(57.2%; p = 0.054)。在所有母亲中,检测到DENV的比例为85.8%。 PCA区分了与最近或以前的ZIKV感染和DENV暴露有关的两个不同的成分。新生儿中的ZIKV NAb高于其相应母亲(p <0.001)。在巴西东北部第一波ZIKV爆发后,我们在母亲中检测到ZIKV暴露的频率很高。但是,我们在小头畸形病例母亲的围产期样本中发现血清标志物对近期感染(IgM和IgG3抗NS1)的敏感性较低。由于中和测试无法准确确定感染时间,因此应尽早在整个怀孕期间进行ZIKV免疫状态测试,以监测流行地区的急性Zika感染。

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