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Biomarkers and immunoprofiles associated with fetal abnormalities of ZIKV-positive pregnancies
Suan-Sin Foo, Weiqiang Chen, Yen Chan, Wai-Suet Lee, Shin-Ae Lee, Genhong Cheng, Karin Nielsen-Saines, Patrícia Brasil, Jae U. Jung
Suan-Sin Foo, Weiqiang Chen, Yen Chan, Wai-Suet Lee, Shin-Ae Lee, Genhong Cheng, Karin Nielsen-Saines, Patrícia Brasil, Jae U. Jung
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Clinical Research and Public Health Infectious disease Reproductive biology

Biomarkers and immunoprofiles associated with fetal abnormalities of ZIKV-positive pregnancies

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Abstract

BACKGROUND. An intricate fetal-maternal immune crosstalk during pregnancy is essential for a healthy birth. Hence, the infection-induced alterations of maternal immunity often lead to adverse outcomes for mother and/or child. The emergence of Zika virus (ZIKV) infection in pregnant women has been associated with more than 3,000 cases of microcephaly and nervous system malformations. METHODS. To explore the potential correlation of ZIKV-induced alteration of maternal immunity with fetal abnormalities, we performed extensive sera immunoprofiling of 74 pregnant women: 30 symptomatic ZIKV+ pregnant patients and 30 healthy pregnant controls in ZIKV-endemic Rio de Janeiro, along with 14 healthy pregnant controls in non-endemic Los Angeles. RESULTS. Extensive multiplexing analysis of 69 cytokines revealed that CXCL10, CCL2, and CCL8 chemokines were specifically associated with symptomatic ZIKV+ infection during pregnancy, and distinct immunoprofiles were detected at different trimesters in ZIKV-infected pregnant women. Intriguingly, the high CCL2 level and its inverse correlation with CD163, TNFRSF1A, and CCL22 levels was apparently associated with ZIKV-induced abnormal birth. CONCLUSION. Our findings provide insights into the alteration of ZIKV-elicited maternal immunity, serving as a potential clinical biomarker platform. FUNDING. NIH (CA200422, CA180779, DE023926, AI073099, AI116585, AI129496, AI140705, AI069120, AI056154, AI078389, AI28697, AI40718 and AI129534-01), Hastings Foundation, Fletcher Jones Foundation, Departamento de Ciência e Tecnologia (DECIT/25000.072811/2016-17) do Ministério da Saúde do Brasil, and Coordenação de Aperfeiçoamento de Pessoal de Nivel Superior CAPES/88887.116627/2016-01.

Authors

Suan-Sin Foo, Weiqiang Chen, Yen Chan, Wai-Suet Lee, Shin-Ae Lee, Genhong Cheng, Karin Nielsen-Saines, Patrícia Brasil, Jae U. Jung

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Figure 5

Biomarkers associated with abnormal fetal outcomes.

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Biomarkers associated with abnormal fetal outcomes.
Multiplex immune pro...
Multiplex immune profiling of 69 inflammatory cytokines and chemokines using serum specimens derived from 14 LA healthy pregnant women (n = 4–5/trimester), 30 RJ healthy pregnant women (n = 10/trimester), and 30 ZIKV+ pregnant women (n = 10/trimester). (A) Heatmap and fold change of 16 inflammatory cytokines significantly upregulated in ZIKV+ women with abnormal birth compared with ZIKV+ women with normal birth. (B) IPA analysis of induced cytokines predicts cellular events associated with maternal-fetal cellular trafficking, inflammation, and tissue fibrosis. (C) Venn diagram representation of cytokines negatively/positively correlated to CCL2 expression in ZIKV+ pregnancy with normal or abnormal birth outcomes. (D) Increased CCL2/CD163, CCL2/TNFRSF1A, and CCL2/CCL22 ratios in ZIKV+ pregnancy with abnormal birth outcomes. Data (mean ± SEM) are presented in the box plot showing upper (75%) and lower (25%) quartiles, with horizontal line as median and whiskers as maximum and minimum values. *P < 0.05, Mann-Whitney U test. Median value of the ratios for LA healthy and RJ healthy controls is represented as blue dotted line and red dotted line, respectively.

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