Evidence map›Paper›PMID 27932620›Full record

Trial reportThe Journal of infectious diseases2017

Dissecting Antibodies Induced by a Chimeric Yellow Fever-Dengue, Live-Attenuated, Tetravalent Dengue Vaccine (CYD-TDV) in Naive and Dengue-Exposed Individuals.

Sandra Henein, Jesica Swanstrom, Anthony M Byers, Janice M Moser, S Farzana Shaik, Matthew Bonaparte, Nicholas Jackson, Bruno Guy, Ralph Baric, Aravinda M de Silva

Open access · bronzeAbstract readClinical Trial
In one paragraph

Trial report in The Journal of infectious diseases, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 89 papers.

0numbers the graph read from it
0cells of the map it votes in
89citing papers in PubMed
13.0field-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

89 citing papers in PubMed, 123 citations in OpenAlex.

  1. Trial
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  5. Viral genetic diversity and protective efficacy of a tetravalent dengue vaccine in two phase 3 trials.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Trial
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  8. Review
  9. Article
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  13. Dengue and severe dengue.Clinical microbiology reviews · 2025
    Review
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  16. Article
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  20. Review

29 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

10 authors at 3 institutions in 2 countries.

Sandra HeneinDepartment of Microbiology and Immunology and.
Jesica SwanstromDepartment of Epidemiology, Gillings School of Public Health, University of North Carolina, Chapel Hill.
Anthony M ByersSanofi Pasteur, Orlando, Florida.
Janice M MoserSanofi Pasteur, Orlando, Florida.
S Farzana ShaikSanofi Pasteur, Orlando, Florida.
Matthew BonaparteSanofi Pasteur, Swiftwater, Pennsylvania.
Nicholas JacksonSanofi Pasteur, Lyon, France.
Bruno GuySanofi Pasteur, Lyon, France.
Ralph BaricDepartment of Microbiology and Immunology and.
Aravinda M de SilvaDepartment of Microbiology and Immunology and.
Sanofi (United States) · USSanofi (France) · FRUniversity of North Carolina at Chapel Hill · US

Funding

PRECLINICAL ASSAYS TO PREDICT TETRAVALENT DENGUE VACCINE EFFICACYR01AI125198 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DESILVA, ARAVINDA M. · 2016 to 2020
$5.7M
NIAID NIH HHS R01 AI125198
6 · The paper itself

Abstract

Sanofi Pasteur has developed a chimeric yellow fever-dengue, live-attenuated, tetravalent dengue vaccine (CYD-TDV) that is currently approved for use in several countries. In clinical trials, CYD-TDV was efficacious at reducing laboratory-confirmed cases of dengue disease. Efficacy varied by dengue virus (DENV) serotype and prevaccination dengue immune status. We compared the properties of antibodies in naive and DENV-exposed individuals who received CYD-TDV. We depleted specific populations of DENV-reactive antibodies from immune serum samples to estimate the contribution of serotype-cross-reactive and type-specific antibodies to neutralization. Subjects with no preexisting immunity to DENV developed neutralizing antibodies to all 4 serotypes of DENV. Further analysis demonstrated that DENV4 was mainly neutralized by type-specific antibodies whereas DENV1, DENV2, and DENV3 were mainly neutralized by serotype cross-reactive antibodies. When subjects with preexisting immunity to DENV were vaccinated, they developed higher levels of neutralizing antibodies than naive subjects who were vaccinated. In preimmune subjects, CYD-TDV boosted cross-reactive neutralizing antibodies while maintaining type-specific neutralizing antibodies acquired before vaccination. Our results demonstrate that the quality of neutralizing antibodies induced by CYD-TDV varies depending on DENV serotype and previous immune status. We discuss the implications of these results for understanding vaccine efficacy.

Indexed as

Antibodies, NeutralizingAntibodies, ViralCell LineDengueDengue VaccinesFlavivirusHumansImmunogenicity, VaccineVaccines, AttenuatedAntibodies, NeutralizingAntibodies, ViralDengue VaccinesVaccines, AttenuatedDengue vaccineflaviviruslive attenuated vaccine.neutralizing antibody

Identifiers

PMID27932620
PMCPMC6392503
OpenAlexW2559855203

What OpenQuestion holds

Textmetadata
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.