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Maternal DTaP immunization and transplacental transfer of pertussis antibodies in Japan
Kazuya Hiiragi1, Ryosuke Shindo1, Tomoyuki Kojima1
1Perinatal Center for Maternity and Neonates, Yokohama City University Medical Center, Yokohama City, Kanagawa, Japan.
Insights
Maternal diphtheria-tetanus-acellular pertussis (DTaP) immunization effectively transfers antibodies across the placenta. This supports DTaP use in Japan for protecting newborns against pertussis when Tdap is unavailable.
Area of Science:
- Immunology
- Maternal-Fetal Medicine
- Vaccinology
Background:
- Maternal pertussis immunization is crucial for protecting infants.
- Japan offers the DTaP vaccine during pregnancy but not the Tdap vaccine.
- Limited data exists on DTaP's antibody transfer efficacy in pregnant individuals.
Purpose of the Study:
- To evaluate transplacental antibody transfer following maternal DTaP immunization.
- To assess pertussis toxin IgG (PT-IgG) and filamentous hemagglutinin IgG (FHA-IgG) levels.
Main Methods:
- An observational study involving 240 pregnant women categorized by antibody status or DTaP vaccination.
- Maternal and cord blood samples were collected and analyzed for PT-IgG and FHA-IgG.
- Groups included antibody-positive, unvaccinated, and DTaP-vaccinated participants.
Main Results:
- The DTaP-vaccinated group showed significantly higher cord blood antibody positivity (94%) compared to unvaccinated (14%).
- Mean PT-IgG and FHA-IgG titers were substantially elevated in the vaccinated group.
- No correlation was found between gestational week at immunization and antibody titers; no serious adverse events were reported.
Conclusions:
- Maternal DTaP immunization facilitates efficient transplacental antibody transfer.
- Findings support the use of maternal DTaP vaccination in Japan to bolster neonatal pertussis immunity.
- This strategy is particularly relevant where the Tdap vaccine is not approved.
Background:
Maternal pertussis immunization prevents severe infection in early infancy. In Japan, the diphtheria-tetanus-acellular pertussis (DTaP) vaccine is available during pregnancy, whereas the tetanus-diphtheria-acellular pertussis (Tdap) vaccine is not approved. Although they share antigens, DTaP includes higher antigen levels than Tdap. Evidence on maternal DTaP immunization and antibody transfer remains limited. This study evaluated transplacental pertussis antibody transfer after maternal DTaP immunization.
Methods:
This single-center observational study included pregnant women who delivered at a tertiary perinatal center (May 2023 and February 2025) classified as antibody-positive (maternal PT-IgG ≥10 EU/mL), unvaccinated (PT-IgG <10 EU/mL without immunization), or vaccinated (PT-IgG <10 EU/mL with DTaP). Maternal and cord blood samples were analyzed for pertussis toxin IgG (PT-IgG) and filamentous hemagglutinin IgG (FHA-IgG).
Results:
We included 240 women (80/group). Cord blood antibody positivity rates were 70%, 94%, and 14% in the antibody-positive, vaccinated, and unvaccinated groups (P < 0.0001). PT-IgG titers were 14.8, 30.0, and 4.41 EU/mL, and FHA-IgG titers were 18.9, 75.3, and 9.52 EU/mL (P < 0.0001). Gestational week at immunization and antibody titers were not correlated, and no serious vaccine-related adverse events occurred.
Conclusions:
Maternal DTaP immunization demonstrated efficient transplacental transfer. These findings support maternal DTaP use in Japan to enhance neonatal protection against pertussis where Tdap is unavailable.
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