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Peer-reviewedCC BYVaccine: X

Respiratory syncytial virus vaccination during pregnancy confers higher anti-RSV IgG concentration in neonatal cord than maternal blood

  1. 1Department of Obstetrics, Gynecology and Oncology of The Provincial Hospital named after L. Rydygier in Toruń, Poland; Corresponding author.
  2. 2Department of Obstetrics, Gynecology and Oncology of The Provincial Hospital named after L. Rydygier in Toruń, Poland; Academy of Applied Medical and Social Sciences, Elbląg, Poland
  3. 3Department of Obstetrics, Gynecology and Oncology of The Provincial Hospital named after L. Rydygier in Toruń, Poland

Abstract

Respiratory syncytial virus (RSV) infects nearly all children under 2 years of age and poses a significant risk, particularly for infants younger than 6 months. Since 2025, pregnant women in Poland have been eligible for free vaccination against RSV. The aim of this study was to evaluate the concentration of anti-RSV IgG antibodies (types A and B) in vaccinated pregnant women at delivery and in umbilical cord blood of their newborns. Anti-RSV IgG levels were measured using the ELISA method in 304 paired maternal and cord blood samples. Vaccination was administered at 27 to 39 weeks of gestation (mean = 32 weeks). Significantly higher concentrations of IgG antibodies were observed in newborns compared to their mothers ( p < 0.0001), with no association with neonatal sex ( p = 0.41). No correlation was found between the interval from maternal vaccination to delivery and antibody levels in either maternal or cord blood. A history of RSV infection in older children did not result in a statistically significant increase in anti-RSV IgG levels in either mothers or newborns. Conclusions: Maternal RSV vaccination, optimally administered during the third trimester, provides effective passive immunity to the newborn through active transplacental antibody transfer. Vaccination should be recommended during each subsequent pregnancy.

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BibTeX
@article{bednarek2026respiratory,
  title = {{Respiratory syncytial virus vaccination during pregnancy confers higher anti-RSV IgG concentration in neonatal cord than maternal blood}},
  author = {Szymon Bednarek and Małgorzata Świątkowska-Freund and Grażyna Misiak},
  journal = {Vaccine: X},
  year = {2026},
  month = oct,
  doi = {10.1016/j.jvacx.2026.100923},
  url = {https://doi.org/10.1016/j.jvacx.2026.100923},
  note = {CC BY},
}
RIS
TY  - JOUR
TI  - Respiratory syncytial virus vaccination during pregnancy confers higher anti-RSV IgG concentration in neonatal cord than maternal blood
AU  - Szymon Bednarek
AU  - Małgorzata Świątkowska-Freund
AU  - Grażyna Misiak
PY  - 2026
DA  - 2026/10/30
JO  - Vaccine: X
DO  - 10.1016/j.jvacx.2026.100923
UR  - https://doi.org/10.1016/j.jvacx.2026.100923
AB  - Respiratory syncytial virus (RSV) infects nearly all children under 2 years of age and poses a significant risk, particularly for infants younger than 6 months. Since 2025, pregnant women in Poland have been eligible for free vaccination against RSV. The aim of this study was to evaluate the concentration of anti-RSV IgG antibodies (types A and B) in vaccinated pregnant women at delivery and in umbilical cord blood of their newborns. Anti-RSV IgG levels were measured using the ELISA method in 304 paired maternal and cord blood samples. Vaccination was administered at 27 to 39 weeks of gestation (mean = 32 weeks). Significantly higher concentrations of IgG antibodies were observed in newborns compared to their mothers ( p < 0.0001), with no association with neonatal sex ( p = 0.41). No correlation was found between the interval from maternal vaccination to delivery and antibody levels in either maternal or cord blood. A history of RSV infection in older children did not result in a statistically significant increase in anti-RSV IgG levels in either mothers or newborns. Conclusions: Maternal RSV vaccination, optimally administered during the third trimester, provides effective passive immunity to the newborn through active transplacental antibody transfer. Vaccination should be recommended during each subsequent pregnancy.
SN  - 2590-1362
ER  -