Evidence map›Paper›PMID 42729394›Full record

ArticleEClinicalMedicine2026

1-Year follow-up evaluation of TAK-003 dengue vaccine effectiveness against symptomatic disease and hospitalisation in adolescents during the 2024-2025 outbreak in São Paulo, Brazil: a test-negative case-control study.

Lisany Krug Mareto, Thiago Sanches Brumatti, Roberto Dias de Oliveira, Patricia Vieira da Silva, Edinéia Ribeiro Dos Santos, Tatiana Lang D'Agostini, Regiane A Cardoso De Paula, Natalie E Dean, Albert I Ko, Derek A T Cummings and 4 more

Abstract read
In one paragraph

Article in EClinicalMedicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–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.

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

1 citing paper in PubMed.

  1. Review
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

14 authors.

Lisany Krug MaretoSchool of Medicine, Federal University of Mato Grosso do Sul, Campo Grande, MS, Brazil.
Thiago Sanches BrumattiDisease Control Coordination of the São Paulo State Department of Health, São Paulo, Brazil.
Roberto Dias de OliveiraState University of Mato Grosso do Sul - UEMS, Dourados, MS, Brazil.
Patricia Vieira da SilvaOswaldo Cruz Foundation, Campo Grande, MS, Brazil.
Edinéia Ribeiro Dos SantosOswaldo Cruz Foundation, Campo Grande, MS, Brazil.
Tatiana Lang D'AgostiniDisease Control Coordination of the São Paulo State Department of Health, São Paulo, Brazil.
Regiane A Cardoso De PaulaDisease Control Coordination of the São Paulo State Department of Health, São Paulo, Brazil.
Natalie E DeanDepartment of Biostatistics and Bioinformatics, Rollins School of Public Health, Emory University, Atlanta, GA, United States.
Albert I KoDepartment of Epidemiology of Microbial Diseases, Yale School of Public Health, New Haven, CT, USA.
Derek A T CummingsJohns Hopkins Bloomberg School of Public Health, Baltimore, USA.
Jason R AndrewsDivision of Infectious Diseases and Geographic Medicine, Stanford University, Stanford, CA, USA.
Matt D T HitchingsDepartment of Biostatistics, University of Florida, Gainesville, FL, USA.
Otavio RanzaniDataHealth Lab, Institut de Recerca Sant Pau (IR SANT PAU), Barcelona, Spain.
Julio CrodaSchool of Medicine, Federal University of Mato Grosso do Sul, Campo Grande, MS, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Dengue is a growing global health threat. Our initial evaluation of the TAK-003 dengue vaccine in adolescents during the 2024 outbreak in São Paulo State, Brazil, showed short-term protection but suggested possible effectiveness waning after 90-days of the first dose, and had limited power to estimate second-dose effectiveness against hospitalisation. We evaluated 1-year vaccine effectiveness against symptomatic, virologically confirmed dengue and dengue hospitalisation in adolescents during 2024-2025, when DENV-1 and DENV-2 predominated in 2024 followed by increasing DENV-3 transmission in 2025. Methods: We did a test-negative case-control study among adolescents aged 10-15 years in São Paulo State between Feb 20, 2024, and Dec 31, 2025. We extracted individual-level information on demographic characteristics, comorbidities, dengue testing, dengue vaccination, hospitalisation, and death during the study period from the national surveillance databases for dengue (SINAN-Dengue; compulsory notification) and the São Paulo State Secretary of Health vaccination registry (Rede Nacional de Dados em Saúde) on Feb 4, 2026. Cases were defined as acute febrile illness episodes with virologically confirmed dengue, as detected by NS1 antigen or RT-PCR testing within 5 days of symptom onset. Controls were test-negative acute febrile illness episodes. Surveillance data were linked to the state vaccination registry. Vaccine effectiveness after one or two TAK-003 doses was estimated with mixed-effects logistic regression. Findings: We analysed 166,390 tests: 65,365 from cases and 101,025 from controls. Vaccine effectiveness against symptomatic dengue was 59.2% (95% CI 56.1-62.0) after one dose and 73.1% (69.1-76.6) after two doses. Against dengue hospitalisation, effectiveness was 74.6% (62.7-82.7) after one dose and 87.9% (73.0-94.6) after two doses. One-dose protection against symptomatic disease showed no evidence of waning over 1-year follow-up: effectiveness was 73.8% (64.7-80.6) at 270-364 days and 76.8% (59.3-86.8) at 365 days or more. Two-dose protection remained stable to 1 year (74.6%, 95% CI 59.0-84.2, at 270-365 days). Findings were robust in sensitivity analyses and comparable during increased DENV-3 circulation. Interpretation: Our findings show that TAK-003 demonstrated sustained 1-year protection against symptomatic dengue and dengue hospitalisation in adolescents during a large outbreak. Notably, a single dose showed sustained effectiveness without evidence of waning over 1 year, generating an important hypothesis regarding dose reduction that warrants continued long-term observational evaluation. A second dose provided optimal protection, particularly against hospitalisation. These findings reinforce the importance of dengue vaccination as a public health measure. Funding: National Council for Scientific and Technological Development.

Indexed as

DengueHospitalisedSymptomaticTAK-003Vaccine

Identifiers

PMID42729394
PMCPMC13562391

What OpenQuestion holds

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Registered trials

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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.