Evidence map›Paper›PMID 40808283›Full record

Trial reportHuman vaccines & immunotherapeutics2025

Safety, immunogenicity and pregnancy outcomes in mothers and infants after vaccination with an adenovirus-vector COVID-19 vaccine during pregnancy.

Gloria Aguilar, Gabriela Tapia-Calle, Cynthia Robinson, Benoit Baron, David Lowson, Bassem Maximos, Veronica V Rezelj, Anne Marit de Groot, Nicole Bet, Vitalija van Paassen and 3 more

Registry-linked trialAbstract readClinical Trial, Phase II
In one paragraph

Trial report in Human vaccines & immunotherapeutics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04765384 (An Open-label, Phase 2 Study to Evaluate the Safety, Reactogenicity, and Immunogenicity of Ad26.COV2.S in Healthy Pregnant Participants), which is not on this 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.

NCT04765384 phase2completednot on this map

An Open-label, Phase 2 Study to Evaluate the Safety, Reactogenicity, and Immunogenicity of Ad26.COV2.S in Healthy Pregnant Participants

TypeinterventionalSponsorJanssen Vaccines & Prevention B.V.Ran2021 to 2023Enrolled51ConditionsCOVID-19 PreventionArmsAd26.COV2.S
3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
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

13 authors.

Gloria AguilarGlobal Medical Affairs, Johnson & Johnson, Leiden, The Netherlands.
Gabriela Tapia-CalleBiomarkers, Viral Vaccines, Johnson & Johnson, Leiden, The Netherlands.
Cynthia RobinsonClinical Research, Johnson & Johnson, Beerse, Belgium.
Benoit BaronBiostatistics, Johnson & Johnson, Leiden, The Netherlands.
David LowsonFSP, Biostatistics, Cytel Statistical Services & Software Ltd, London, UK.
Bassem MaximosMaximos OB/GYN, League City, TX, USA.
Veronica V RezeljBiomarkers, Viral Vaccines, Johnson & Johnson, Leiden, The Netherlands.
Anne Marit de GrootClinical Immunology, Johnson & Johnson, Leiden, The Netherlands.
Nicole BetClinical Immunology, Johnson & Johnson, Leiden, The Netherlands.
Vitalija van PaassenBiostatistics, Johnson & Johnson, Leiden, The Netherlands.
Mathieu Le GarsBiomarkers, Viral Vaccines, Johnson & Johnson, Leiden, The Netherlands.
Frank StruyfScientific Affairs and Late Development, Johnson & Johnson, Beerse, Belgium.
Javier Ruiz-GuiñazúCrucell Integration, Johnson & Johnson, Beerse, Belgium.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

COVID-19 during pregnancy can be associated with adverse pregnancy and infant outcomes. We assessed the safety, reactogenicity, and immunogenicity of maternal vaccination with Ad26.COV2.S COVID-19 vaccine and monitored serum and breast milk antibody levels in mothers and infants until 6 months post-delivery. This open-label Phase 2 study enrolled previously COVID-19 vaccinated or COVID-19-vaccine-naive healthy pregnant women in trimester two or three (NCT04765384). All women received a single dose of Ad26.COV2.S. Mothers and infants were followed-up for safety until 1-year post-partum and for immunogenicity, including antibodies in breast milk, until 6 months post-partum. Recruitment was stopped at 51 participants due to rapidity of roll-out of COVID-19 vaccines recommended during pregnancy. Ad26.COV2.S was well-tolerated regardless of previous COVID-19 vaccination history. All pregnancies resulted in a live infant, four were preterm. One serious adverse event of placental insufficiency Day-36 post-vaccination was considered vaccine-related by the investigator. One infant died due to complications associated with an unrelated ventricular septal defect. Ad26.COV2.S induced robust immune responses in women with different COVID-19 vaccination histories. Spike-binding antibody (SAbs) and virus neutralizing antibody (NAbs) titers at delivery tended to be higher in mothers vaccinated during trimester three. Maternal serum and cord blood were strongly correlated. 100% of infants had detectable SAbs at aged 6 months, and 70.6% had detectable NAbs, including 68.2% born to initially vaccine-naïve mothers. Maternal vaccination with an adenovirus-vector vaccine was well-tolerated and immunogenic in mothers and infants. These data could support the adoption of heterologous booster regimens during pregnancy and future adenovirus-vector vaccine development.

Indexed as

COVID-19COVID-19 VaccinesImmunogenicity, VaccinePregnancy Complications, InfectiousAdenoviridaeAdultAntibodies, NeutralizingAntibodies, ViralFemaleHumansInfantInfant, NewbornMilk, HumanPregnancyPregnancy OutcomeSARS-CoV-2Antibodies, NeutralizingAntibodies, ViralCOVID-19 VaccinesAdenovirus vectorsCOVID-19neonatespassive antibody transferpregnancySARS-CoV-2vaccine

Identifiers

PMID40808283
PMCPMC12355676

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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.