Evidence map›Paper›PMID 29282215›Full record

ReviewEMBO reports2018

The bright and the dark side of human antibody responses to flaviviruses: lessons for vaccine design.

Félix A Rey, Karin Stiasny, Marie-Christine Vaney, Mariano Dellarole, Franz X Heinz

Open access · hybridAbstract readReview
In one paragraph

Review in EMBO reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 161 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
161citing papers in PubMed, 1 pooled it
24.6field-weighted citation impact, top 1% 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

161 citing papers in PubMed, 1 synthesis or guideline pooled it, 247 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Lipid Architecture in the Zika Virus.ACS physical chemistry Au · 2026
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101 more citing papers are in PubMed but not listed here.

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

5 authors at 2 institutions in 2 countries.

Félix A ReyStructural Virology Unit, Virology Department, Institut Pasteur, Paris, France felix.rey@pasteur.fr franz.x.heinz@meduniwien.ac.at.ORCID 0000-0002-9953-7988
Karin StiasnyCenter for Virology, Medical University of Vienna, Vienna, Austria.
Marie-Christine VaneyStructural Virology Unit, Virology Department, Institut Pasteur, Paris, France.
Mariano DellaroleStructural Virology Unit, Virology Department, Institut Pasteur, Paris, France.
Franz X HeinzCenter for Virology, Medical University of Vienna, Vienna, Austria felix.rey@pasteur.fr franz.x.heinz@meduniwien.ac.at.ORCID 0000-0002-7191-4331
Centre National de la Recherche Scientifique · FRMedical University of Vienna · AT

Funding

Austrian Science Fund FWF I 1378Austrian Science Fund FWF P 25265Austrian Science Fund FWF P 27501Austrian Science Fund FWF P 29928
6 · The paper itself

Abstract

Zika and dengue viruses belong to the Flavivirus genus, a close group of antigenically related viruses that cause significant arthropod-transmitted diseases throughout the globe. Although infection by a given flavivirus is thought to confer lifelong protection, some of the patient's antibodies cross-react with other flaviviruses without cross-neutralizing. The original antigenic sin phenomenon may amplify such antibodies upon subsequent heterologous flavivirus infection, potentially aggravating disease by antibody-dependent enhancement (ADE). The most striking example is provided by the four different dengue viruses, where infection by one serotype appears to predispose to more severe disease upon infection by a second one. A similar effect was postulated for sequential infections with Zika and dengue viruses. In this review, we analyze the molecular determinants of the dual antibody response to flavivirus infection or vaccination in humans. We highlight the role of conserved partially cryptic epitopes giving rise to cross-reacting and poorly neutralizing, ADE-prone antibodies. We end by proposing a strategy for developing an epitope-focused vaccine approach to avoid eliciting undesirable antibodies while focusing the immune system on producing protective antibodies only.

Indexed as

AnimalsAntibodies, NeutralizingAntibodies, ViralAntibody FormationAntigens, ViralEpitopesFlavivirusFlavivirus InfectionsHumansImmunizationViral VaccinesAntibodies, NeutralizingAntibodies, ViralAntigens, ViralEpitopesViral Vaccinesantibody‐dependent enhancementantibody neutralizationflavivirus structureparticle heterogeneityvaccine design

Identifiers

PMID29282215
PMCPMC5797954
OpenAlexW2777057590

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.