Evidence map›Paper›PMID 32542479›Full record

Observational studyVirus genes2020

Rapid decline of Zika virus NS1 antigen-specific antibody responses, northeastern Brazil.

Andres Moreira-Soto, Gilmara de Souza Sampaio, Célia Pedroso, Ignacio Postigo-Hidalgo, Beatrice Sarah Berneck, Sebastian Ulbert, Carlos Brites, Eduardo Martins Netto, Jan Felix Drexler

Open access · hybridAbstract readObservational Study
In one paragraph

Observational study in Virus genes, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.3field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Analysis of Zika Virus Sequence Data Associated with a School Cohort in Haiti.The American journal of tropical medicine and hygiene · 2022
    Article
  5. Article
  6. Article
  7. Article
  8. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 3 countries.

Andres Moreira-SotoCharité-Universitätsmedizin Berlin, Humboldt-Universität Zu Berlin, and Berlin Institute of Health, Institute of Virology, Berlin, Germany.
Gilmara de Souza SampaioUniversidade Federal da Bahia, Salvador, Bahia, Brasil.
Célia PedrosoUniversidade Federal da Bahia, Salvador, Bahia, Brasil.
Ignacio Postigo-HidalgoCharité-Universitätsmedizin Berlin, Humboldt-Universität Zu Berlin, and Berlin Institute of Health, Institute of Virology, Berlin, Germany.
Beatrice Sarah BerneckDepartment of Immunology, Fraunhofer Institute for Cell Therapy and Immunology, Leipzig, Germany.
Sebastian UlbertDepartment of Immunology, Fraunhofer Institute for Cell Therapy and Immunology, Leipzig, Germany.
Carlos BritesUniversidade Federal da Bahia, Salvador, Bahia, Brasil.
Eduardo Martins NettoUniversidade Federal da Bahia, Salvador, Bahia, Brasil.
Jan Felix DrexlerCharité-Universitätsmedizin Berlin, Humboldt-Universität Zu Berlin, and Berlin Institute of Health, Institute of Virology, Berlin, Germany. felix.drexler@charite.de.ORCID http://orcid.org/0000-0002-3509-0232
Universidade Federal da Bahia · BRCharité - Universitätsmedizin Berlin · DEFraunhofer Institute for Cell Therapy and Immunology · DEHumboldt-Universität zu Berlin · DE

Funding

Honours 721367Horizon 2020 734548
6 · The paper itself

Abstract

Zika virus (ZIKV) is a positive-stranded RNA virus within the Flaviviridae family. After decades of circulation in Asia, ZIKV was introduced to Brazil in 2014-2015, associated with a rise in congenital malformations. Unlike the genetically related dengue virus (DENV), ZIKV constitutes only one serotype. Although assumed that ZIKV infection may engender lifelong immunity, the long-term kinetics of ZIKV antibody responses are unclear. We assessed long-term kinetics of ZIKV NS1-IgG response in 144 individuals from 3 different subpopulations: HIV patients, tuberculosis patients and healthy individuals first tested in 2016 and retested 1.5-2 years after the 2015-2016 ZIKV epidemic in Salvador de Bahia, Brazil, using a widely distributed NS1-based commercial ELISA. The seropositivity in 2016 reached 59.0% (85/144, 95% confidence interval (CI) 50.7-66.7%), and decreased to 38.6% (56/144, CI 31.3-47.0%) 1.5-2 years later. In addition, the median ZIKV NS1-ELISA reactivity for individuals that remained positive in both timepoints significantly decreased from a ratio of 4.4 (95% CI 3.8-5.0) to 1.6 (95% CI 1.6-1.9) over the 2-year interval (Z: - 6.1; p < 0.001) irrespective of the subpopulation analyzed. Initial 2016 DENV antibody response was non-significant between groups, suggesting comparable DENV background. The high 20.6% seroreversion suggest that widely used serologic tests may fail to account a considerable proportion of past ZIKV infections in flavivirus endemic countries. In addition, ZIKV immunity might be shorter-lived than previously thought, which may contribute to local ZIKV resurgence once individual immune responses wane sufficiently to reduce community protective immunity in addition to birth and migration.

Indexed as

Zika Virus InfectionAntibodies, ViralBrazilComorbidityCross-Sectional StudiesHIV InfectionsHumansImmunoglobulin GProspective StudiesTuberculosisViral Nonstructural ProteinsZika VirusAntibodies, ViralImmunoglobulin GNS1 protein, zika virusViral Nonstructural ProteinsAntigensFlavivirusSerologyZika virus

Identifiers

PMID32542479
PMCPMC7294518
OpenAlexW3034992871

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.