Antibody in Breastmilk Following Pertussis Vaccination in Three-time Windows in Pregnancy

Olwenn Daniel1, Myles Loughnan1,2, Miranda Quenby1,3

  • 1From the Centre for Neonatal and Paediatric Infection and Vaccine Institute, School of Health & Medical Sciences, City St George's, London, UK.

Insights

Maternal pertussis vaccination timing during pregnancy does not affect specific IgA levels in breast milk. This finding is crucial for optimizing infant mucosal immunity through breastfeeding after maternal immunization.

Area of Science:

  • Immunology
  • Maternal and Infant Health
  • Vaccinology

Background:

  • Pertussis-containing vaccines are recommended during pregnancy in the UK (16-32 weeks gestation).
  • Debate exists regarding optimal vaccination timing for maternal and infant benefits.
  • Breast milk IgA is vital for infant mucosal immunity, and its concentration may be influenced by maternal vaccination timing.

Purpose of the Study:

  • To investigate if the timing of maternal pertussis vaccination during pregnancy impacts breast milk IgA concentrations.
  • To assess antigen-specific IgA levels in colostrum and mature breast milk following different vaccination schedules.

Main Methods:

  • Participants received pertussis-containing vaccines at different gestational periods (before 24 weeks, 24-27+6 weeks, or 28-31+6 weeks).
  • Colostrum and breast milk samples were collected within 24 hours of delivery and at 14 days postpartum, respectively.
  • Multiplex immunoassay was used to measure specific IgA levels against pertussis toxin, pertactin, tetanus toxoid, and diphtheria toxoid.

Main Results:

  • No significant differences in specific IgA levels against tested antigens were observed between vaccination timing groups.
  • A general decline in antigen-specific IgA levels was noted from colostrum to breast milk at 14 days postpartum for all participants.

Conclusions:

  • The timing of pertussis-containing vaccine administration during pregnancy does not appear to influence the concentration of antigen-specific IgA in colostrum or breast milk at 14 days.
  • These findings support current vaccination guidelines, suggesting flexibility in timing without compromising this aspect of passive immunity transfer.
Abstract

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