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

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-...

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Vydáno v:Human vaccines & immunotherapeutics Ročník 21; číslo 1; s. 2538340
Hlavní autoři: Aguilar, Gloria, Tapia-Calle, Gabriela, Robinson, Cynthia, Baron, Benoit, Lowson, David, Maximos, Bassem, Rezelj, Veronica V., de Groot, Anne Marit, Bet, Nicole, van Paassen, Vitalija, Le Gars, Mathieu, Struyf, Frank, Ruiz-Guiñazú, Javier
Médium: Journal Article
Jazyk:angličtina
Vydáno: United States Taylor & Francis 01.12.2025
Taylor & Francis Group
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ISSN:2164-5515, 2164-554X, 2164-554X
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Shrnutí: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.
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Present address: GSK, Avenue Fleming 20, 1300 Wavre, Belgium.
Present address: AstraZeneca, Barcelona, Spain.
ISSN:2164-5515
2164-554X
2164-554X
DOI:10.1080/21645515.2025.2538340