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Published on: August 7, 2017
Prevalence of pertussis antibodies in maternal delivery, cord, and infant serum
C Mary Healy1, Flor M Munoz, Marcia A Rench
1Section of Infectious Diseases, Department of Pediatrics, Baylor College of Medicine, Houston, Texas, USA. chealy@bcm.tmc.edu
Insights
Maternal antibodies offer infant protection, but low pertussis antibody levels and rapid decay leave newborns vulnerable. This highlights the need for maternal immunization strategies against pertussis.
Area of Science:
- Immunology
- Pediatrics
- Vaccinology
Background:
- Passively acquired maternal antibodies are crucial for infant protection against pathogens.
- Increasing pertussis (whooping cough) cases in infants necessitate evaluating antibody levels.
Purpose of the Study:
- To assess pertussis antibody levels in maternal-infant pairs.
- To determine the extent of placental transfer and infant antibody decay.
Main Methods:
- Used IgG-specific ELISA to measure antibodies against pertussis toxin (PT), filamentous hemagglutinin (FHA), and fimbrial proteins (FIM).
- Analyzed 64 maternal-umbilical cord serum pairs and 61 infant sera.
- Calculated geometric mean concentrations (GMCs) and cord:maternal GMC ratios.
Main Results:
- Maternal antibody GMCs at delivery were low for PT, FHA, and FIM.
- Efficient placental transfer occurred, with cord GMCs significantly higher than maternal levels (157-178% of maternal values).
- Infant pertussis-specific IgG decayed below detectable levels by 2 months of age.
Conclusions:
- Despite efficient transfer, low maternal antibody levels and rapid infant decay provide insufficient protection against pertussis.
- Supports maternal or neonatal immunization with acellular pertussis vaccines to protect infants.
- Urgent need for strategies to prevent severe infant pertussis.
Background:
Passively acquired maternal antibodies protect infants from many pathogens. With increasing reports of infant pertussis, we evaluated pertussis antibodies in maternal-infant paired sera from 1999-2000.
Methods:
Antibodies to pertussis toxin (PT), filamentous hemagglutinin (FHA), and fimbrial proteins (FIM) were measured by validated IgG-specific enzyme-linked immunosorbant assay (ELISA) in 64 maternal-umbilical cord serum pairs and in 61 of 64 infant sera. Geometric mean concentrations (GMCs) of pertussis antibodies and cord : maternal GMC ratios were calculated.
Results:
Mean maternal age and gestation were 29.7 years (range, 19-42) and 39.3 weeks (range, 35.6-40.9), and 81% of mothers were white. GMCs of maternal antibodies at delivery (ELISA units/mL) were 2.4 for PT, 6.9 for FHA, and 13 for FIM. Cord GMCs were 169%, 178%, and 157% of maternal delivery values for PT, FHA, and FIM, respectively, demonstrating active placental transfer (P<.001). Pertussis-specific IgG values for each antigen decayed to below the threshold of detection by age 2 months.
Conclusions:
Despite efficient placental transfer, low maternal pertussis antibody levels and their rapid decay in infant sera leave infants with little humoral protection against pertussis. These data support the rationale for maternal or neonatal immunization, with acellular pertussis vaccines, to prevent life-threatening pertussis in early infancy.
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