Evidence map›Paper›PMID 41505490›Full record

ArticlePLoS neglected tropical diseases2026

Zika virus infection in early pregnancy increases the likelihood of persistent neutralizing antibodies.

Everton Falcão de Oliveira, Amanda Torrentes de Carvalho, Fabio Antonio Venancio, Maria Eulina Quilião, Sanny Cerqueira de Oliveira Gabeira, Silvia Helena Dos Santos Leite, Margarida Dos Santos Salú, Sheila Maria Barbosa de Lima, Nathalia Dos Santos Alves, Luma da Cruz Moura and 15 more

Abstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

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4 · The record

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5 · Who and what money

Authors and funding

25 authors.

Everton Falcão de OliveiraFaculdade de Medicina, Universidade Federal de Mato Grosso do Sul, Campo Grande, Brazil.ORCID https://orcid.org/0000-0002-0074-5278
Amanda Torrentes de CarvalhoLaboratório de Imunobiologia das Doenças Infecciosas, Departamento de Imunobiologia, Universidade Federal Fluminense, Niterói, Brazil.
Fabio Antonio VenancioPrograma de Pós-Graduação em Doenças Infecciosas e Parasitárias, Universidade Federal de Mato Grosso do Sul, Campo Grande, Brazil.
Maria Eulina QuiliãoCentro Especializado em Reabilitação da Associação de Pais e Amigos dos Excepcionais, Campo Grande, Brazil.
Sanny Cerqueira de Oliveira GabeiraLaboratório de Alta Complexidade, Instituto Nacional de Saúde da Mulher, da Criança e do Adolescente Fernandes Figueira, Fiocruz, Rio de Janeiro, Brazil.
Silvia Helena Dos Santos LeiteLaboratório de Alta Complexidade, Instituto Nacional de Saúde da Mulher, da Criança e do Adolescente Fernandes Figueira, Fiocruz, Rio de Janeiro, Brazil.
Margarida Dos Santos SalúLaboratório de Alta Complexidade, Instituto Nacional de Saúde da Mulher, da Criança e do Adolescente Fernandes Figueira, Fiocruz, Rio de Janeiro, Brazil.
Sheila Maria Barbosa de LimaDepartamento de Desenvolvimento Experimental e Pré-Clínico, Fiocruz, Rio de Janeiro, Brazil.
Nathalia Dos Santos AlvesLaboratório de Análise Imunomolecular, Bio-Manguinhos, Fiocruz, Rio de Janeiro, Brazil.
Luma da Cruz MouraLaboratório de Análise Imunomolecular, Bio-Manguinhos, Fiocruz, Rio de Janeiro, Brazil.
Waleska Dias SchwarczLaboratório de Análise Imunomolecular, Bio-Manguinhos, Fiocruz, Rio de Janeiro, Brazil.
Adriana de Souza AzevedoLaboratório de Análise Imunomolecular, Bio-Manguinhos, Fiocruz, Rio de Janeiro, Brazil.
Luiz Henrique Ferraz DemarchiLaboratório Central de Saúde Pública de Mato Grosso do Sul, Secretaria de Estado de Saúde de Mato Grosso do Sul, Campo Grande, Brazil.
Marina Castilhos Souza Umaki ZardinLaboratório Central de Saúde Pública de Mato Grosso do Sul, Secretaria de Estado de Saúde de Mato Grosso do Sul, Campo Grande, Brazil.
Gislene Garcia de Castro LichsLaboratório Central de Saúde Pública de Mato Grosso do Sul, Secretaria de Estado de Saúde de Mato Grosso do Sul, Campo Grande, Brazil.
Deborah Ledesma TairaLaboratório Central de Saúde Pública de Mato Grosso do Sul, Secretaria de Estado de Saúde de Mato Grosso do Sul, Campo Grande, Brazil.
Ana Isabel do NascimentoPrograma de Pós-Graduação em Doenças Infecciosas e Parasitárias, Universidade Federal de Mato Grosso do Sul, Campo Grande, Brazil.
Wagner de Souza FernandesInstituto de Biociências, Laboratório de Parasitologia Humana, Universidade Federal de Mato Grosso do Sul, Campo Grande, Brazil.
Natália Oliveira AlvesPrograma de Pós-Graduação em Doenças Infecciosas e Parasitárias, Universidade Federal de Mato Grosso do Sul, Campo Grande, Brazil.
Aline Etelvina Casaril ArruaInstituto de Biociências, Laboratório de Parasitologia Humana, Universidade Federal de Mato Grosso do Sul, Campo Grande, Brazil.
Márcio José de MedeirosUniversidade Federal do Rio de Janeiro, Campus Macaé, Rio de Janeiro, RJ, Brazil.
Rivaldo Venâncio da CunhaPrograma de Pós-Graduação em Doenças Infecciosas e Parasitárias, Universidade Federal de Mato Grosso do Sul, Campo Grande, Brazil.
Zilton VasconcelosLaboratório de Alta Complexidade, Instituto Nacional de Saúde da Mulher, da Criança e do Adolescente Fernandes Figueira, Fiocruz, Rio de Janeiro, Brazil.
Cláudia Du Bocage Santos-PintoFaculdade de Medicina, Universidade Federal de Mato Grosso do Sul, Campo Grande, Brazil.
Karin Nielsen-SainesDavid Geffen School of Medicine at the University of California, Los Angeles (UCLA), Los Angeles, California, United States of America.ORCID https://orcid.org/0000-0002-1742-5211

Funding

Genetic evolution, pathogenesis and immune responses in mother to child transmission of ZIKVR01AI140718 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI CHENG, GENHONG, JUNG, JAE U · 2018 to 2022
$3.8M
NIAID NIH HHS R01 AI140718
6 · The paper itself

Abstract

backgroundNeutralizing antibodies (nAbs) play a central role in protection against Zika virus (ZIKV) infection. Higher maternal ZIKV nAb titers during pregnancy have been associated with reduced risk of congenital anomalies. However, limited data exist on the long-term persistence of these antibodies in women infected during pregnancy and in children exposed in utero. METHODOLOGY/PRINCIPAL

findingsWe conducted a cross-sectional serological study using stored serum samples from a cohort of mother-child pairs with confirmed maternal ZIKV infection during pregnancy in Campo Grande, Brazil. ZIKV nAb titers were measured in samples collected approximately 3-4 years after maternal infection using plaque reduction neutralization testing. Among 77 women, 66.2% (51/77) had ZIKV nAbs above the cutoff point, with higher titers observed in patients with first trimester infection. In contrast, only 2 of 72 children (2.8%) presented detectable ZIKV nAbs following clearance of maternal antibodies. No clear association was found between maternal nAb titers and adverse child outcomes. CONCLUSIONS/SIGNIFICANCE: Our findings suggest long-term persistence of neutralizing antibodies in most women infected with ZIKV during pregnancy, especially when infection occurred in the first trimester of pregnancy ZIKV-specific nAb persistence was rare in children with antenatal exposure once maternal antibodies waned, reinforcing concerns about limited postnatal protection in this group. These results underscore the importance of further studies to clarify the role of neutralizing antibodies in long-term protection and disease pathogenesis, particularly in endemic regions where the risk of reinfection or exposure to related arboviruses remains high.

Indexed as

Antibodies, NeutralizingAntibodies, ViralPregnancy Complications, InfectiousZika VirusZika Virus InfectionAdultBrazilCross-Sectional StudiesFemaleHumansNeutralization TestsPregnancyYoung AdultAntibodies, NeutralizingAntibodies, Viral

Identifiers

PMID41505490
PMCPMC12810899

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.