Evidence map›Paper›PMID 37971871›Full record

ArticleThe Journal of clinical investigation2024

TV005 dengue vaccine protects against dengue serotypes 2 and 3 in two controlled human infection studies.

Kristen K Pierce, Anna P Durbin, Mary-Claire R Walsh, Marya Carmolli, Beulah P Sabundayo, Dorothy M Dickson, Sean A Diehl, Stephen S Whitehead, Beth D Kirkpatrick

4 registry-linked trialsAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 4 registered trials, which are not on this map. Cited by 27 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 2 pooled it
–field-weighted citation impact
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.

NCT02317900 phase1completednot on this map

A Phase 1 Evaluation of the Safety and Protective Efficacy of a Single Dose of the Live Attenuated Tetravalent Dengue Vaccine TV005 to Protect Against Infection With Attenuated DENV-2, rDEN2∆30-7169

TypeinterventionalSponsorNational Institute of Allergy and Infectious Diseases (NIAID)Ran2014Enrolled48ConditionsDengueArmsTV005, Placebo, rDEN2∆30-7169
NCT02873260 phase1completednot on this map

A Phase 1 Evaluation of the Safety and Protective Efficacy of a Single Dose of the Live Attenuated Tetravalent Dengue Vaccine TV005 to Protect Against Infection With rDEN3Δ30

TypeinterventionalSponsorNational Institute of Allergy and Infectious Diseases (NIAID)Ran2016 to 2017Enrolled48ConditionsDengueArmsTetraVax-DV-TV005, rDEN3Δ30, Placebo
NCT06805487 phase1completednot on this map

A Phase 1 Evaluation of the Protective Efficacy of a Single Dose of the Live Attenuated Tetravalent Dengue Vaccine TV003 or Previous Zika Infection Against Infection With ZIKV-SJRP Challenge Compared to DENV and ZIKV-naïve Historical Controls Against Infection With ZIKV-SJRP Challenge

TypeinterventionalSponsorNational Institute of Allergy and Infectious Diseases (NIAID)Ran2024 to 2025Enrolled27ConditionsZika VirusArmsTetraVax-DV-TV003 (TV003), Plasmalyte, Challenge virus ZIKV-SJRP/2016-184
NCT07412483 narecruitingnot on this mapstarted 2026, after this paper: background citation

A Controlled Human Infection Model of Dengue

TypeinterventionalSponsorTan Tock Seng HospitalRan2026 to 2029Enrolled5ConditionsDengueArmsGMP-produced rDEN3delta30 virus
3 · Its place in the literature

Who cites it

27 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
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  6. Article
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  12. Dengue is Still a Complicated Disease.Combinatorial chemistry & high throughput screening · 2026
    Article
  13. Article
  14. Dengue and severe dengue.Clinical microbiology reviews · 2025
    Review
  15. Article
  16. Review
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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.

Kristen K PierceDepartment of Medicine and.
Anna P DurbinThe Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.
Mary-Claire R WalshDepartment of Medicine and.
Marya CarmolliDepartment of Microbiology and Molecular Genetics, The University of Vermont Larner College of Medicine, Vaccine Testing Center, Burlington, Vermont, USA.
Beulah P SabundayoThe Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.
Dorothy M DicksonDepartment of Microbiology and Molecular Genetics, The University of Vermont Larner College of Medicine, Vaccine Testing Center, Burlington, Vermont, USA.
Sean A DiehlDepartment of Microbiology and Molecular Genetics, The University of Vermont Larner College of Medicine, Vaccine Testing Center, Burlington, Vermont, USA.
Stephen S WhiteheadNational Institute of Allergy and Infectious Diseases (NIAID), Laboratory of Viral Diseases, Bethesda, Maryland, USA.
Beth D KirkpatrickDepartment of Medicine and.

Funding

Clinical Trials of Biodefense Vaccines (Dengue, West Nile Virus, TBEV)ZIAAI000987 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI WHITEHEAD, STEPHEN · 2009 to 2025
$37.9M
A Phase II Evaluation of the Safety and Protective Efficacy of the Live Attenuated Tetravalent Dengue Vaccine TetraVax-DV with Challenge by the Recombinant DENV-2 Virus in a Dengue Endemic PopulationU01AI134582 · NIAID · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI KIRKPATRICK, BETH DIANE · 2019 to 2024
$6.3M
Mechanisms of Protection and Durability for a Live Attenuated Tetravalent Dengue VaccineU01AI141997 · NIAID · UNIVERSITY OF VERMONT & ST AGRIC COLLEGE · PI Sean A. Diehl, Anna Palmer Durbin · 2019 to 2026
$5.1M
NIAID NIH HHS HHSN272200900010CNIAID NIH HHS U01 AI134582NIAID NIH HHS U01 AI141997
6 · The paper itself

Abstract

BACKGROUNDDisease due to dengue viruses is a growing global health threat, causing 100-400 million cases annually. An ideal dengue vaccine should demonstrate durable protection against all 4 serotypes in phase III efficacy trials, however the lack of circulating serotypes may lead to incomplete efficacy data. Controlled human infection models help downselect vaccine candidates and supply critical data to supplement efficacy trials. We evaluated the efficacy of a leading live-attenuated tetravalent dengue vaccine candidate, TV005, against infection with a newly established dengue serotype 3 or an established serotype 2 challenge virus.METHODSTwo randomized, controlled clinical trials were performed. In study 1, a total of 42 participants received TV005 or placebo (n = 21 each), and 6 months later, all were challenged with dengue 2 virus (rDEN2Δ30) at a dose of 103 PFU. In study 2, a total of 23 participants received TV005 and 20 received placebo, and 6 months later, all were challenged with 104 PFU dengue 3 virus (rDEN3Δ30). The study participants were closely monitored for safety, viremia, and immunologic responses. Infection, measured by post-challenge viremia, and the occurrence of rash and neutropenia were the primary endpoints. Secondary endpoints included safety, immunologic, and virologic profiles following vaccination with TV005 and subsequent challenge with the rDEN2Δ30 or rDEN3Δ30 strain.RESULTSTV005 was well tolerated and protected all vaccinated volunteers from viremia with DENV2 or DENV3 (none infected in either group). Placebo recipients had post-challenge viremia (100% in study 1, 85% in study 2), and all experienced rash following challenge with either serotype.CONCLUSIONSTV005 is a leading tetravalent dengue vaccine candidate that fully protected against infection with DENV2 and DENV3 in an established controlled human infection model.TRIAL REGISTRATIONClinicalTrials.gov NCT02317900 and NCT02873260.FUNDINGIntramural Research Program, NIH (contract HHSN272200900010C).

Indexed as

DengueDengue VaccinesDengue VirusExanthemaAntibodies, ViralHumansSerogroupVaccines, AttenuatedViremiaAntibodies, ViralDengue VaccinesVaccines, AttenuatedAIDS vaccineInfectious disease

Identifiers

PMID37971871
PMCPMC10836801

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.