Evidence map›Paper›PMID 42558730›Full record

ReviewFrontiers in immunology2026

Mapping immune responses to TAK-003 dengue vaccine: immunogenicity across the clinical development program.

Sanja Mandaric, Tarek El Hindi, Eduardo J M Nascimento, Xavier Saez-Llorens, Charissa Borja-Tabora, Heather Friberg, Vianney Tricou, Nicholas Roubinis, Raphael Gottardo, Jeffrey R Currier and 2 more

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Sanja MandaricTakeda Pharmaceuticals International AG, Zurich, Switzerland.
Tarek El HindiTakeda Pharmaceuticals International AG, Zurich, Switzerland.
Eduardo J M NascimentoTakeda Vaccines, Inc., Cambridge, MA, United States.
Xavier Saez-LlorensPediatric Infectious Diseases, Hospital del Niño Dr. José Renán Esquivel, Sistema Nacional de Investigación at SENACYT, Centro de Vacunación Internacional (Cevaxin), Panama City, Panama.
Charissa Borja-TaboraClinical Research Division, Research Institute for Tropical Medicine, Muntinlupa, Philippines.
Heather FribergViral Diseases Program, Center for Infectious Disease Research, Walter Reed Army Institute of Research, Silver Spring, MD, United States.
Vianney TricouTakeda Pharmaceuticals International AG, Zurich, Switzerland.
Nicholas RoubinisTakeda Pharmaceuticals International AG, Zurich, Switzerland.
Raphael GottardoLausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
Jeffrey R CurrierViral Diseases Program, Center for Infectious Disease Research, Walter Reed Army Institute of Research, Silver Spring, MD, United States.
Mayuri SharmaTakeda Vaccines, Inc., Cambridge, MA, United States.
Shibadas BiswalTakeda Vaccines, Inc., Cambridge, MA, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite deployment of vector control and prevention strategies, dengue remains a substantial threat to public health. Development of an effective vaccine against dengue has been challenging due to the need for simultaneous immunity against all four dengue virus serotypes, durable protection regardless of prior dengue exposure, and the complex epidemiological patterns of serotype co-circulation. As part of the clinical development of TAK-003, a live attenuated tetravalent dengue vaccine based on a DENV-2 backbone, extensive profiling of post-vaccination immune responses has been performed in participants who were dengue-naive or previously-exposed at baseline across dengue-endemic and non-endemic regions. In this review, we summarise the magnitude, quality, and functionality of humoral and cellular immune responses following the first and second doses of TAK-003 across age, region, and DENV serotype. We also outline long-term persistence and durability, ongoing investigations into correlates of protection, age-stratified responses, and evidence on co-administration with other vaccines.

Indexed as

DengueDengue VaccinesDengue VirusImmunogenicity, VaccineAnimalsAntibodies, NeutralizingAntibodies, ViralHumansImmunity, CellularImmunity, HumoralVaccine DevelopmentVaccines, AttenuatedAntibodies, NeutralizingAntibodies, ViralDengue VaccinesVaccines, Attenuatedcellular immunitydenguehumoral immunityimmunogenicityneutralising antibodiesTAK-003T-cells

Identifiers

PMID42558730
PMCPMC13438160

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.