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Author Notes:

E-mail: Elizabeth.Schlaudecker@cchmc.org

Conceived and designed the experiments: MCS SBO ER SEA RR RFB KZ.

Performed the experiments: EPS MMM KZ.

Analyzed the data: EPS MCS MMM CND KZ.

Contributed reagents/materials/analysis tools: MMM CND.

Wrote the paper: EPS MCS SBO MMM ER SEA CND RR RFB KZ.

We thank all of the women and infants who participated in the trial; the Ethical Review Committee at the International Centre for Diarrheal Disease Research, Bangladesh; the Institutional Review Board (IRB) at Cincinnati Children's Hospital Medical Center, Cincinnati; and the IRB at the Bloomberg School of Public Health at Johns Hopkins University, Baltimore.

MCS reports receiving research support from Wyeth and Sanofi-Aventis for other studies and lecture fees from GlaxoSmithKline, Aventis Pasteur, and Sanofi-Aventis.

This study was also partly funded by Aventis Pasteur.

Fluarix is a GlaxoSmithKline product, but this product was purchased directly from the manufacturer with no funding support from GlaxoSmithKline.

There are no further patents, products in development or marketed products to declare.

This does not alter the authors' adherence to all the PLOS ONE policies on sharing data and materials.

Subjects:

Research Funding:

This work was supported by the Bill and Melinda Gates Foundation; a cooperative agreement (HRN-A-0096-90006-00) with the United States Agency for International Development; the Department of Health and Human Services; the National Vaccine Program Office; Wyeth Pharmaceuticals; the Thrasher Research Fund; Aventis Pasteur; the International Centre for Diarrheal Disease Research; and the Bloomberg School of Public Health at Johns Hopkins University.

The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Keywords:

  • Science & Technology
  • Multidisciplinary Sciences
  • Science & Technology - Other Topics
  • BREAST-MILK
  • MATERNAL IMMUNIZATION
  • IMMUNE-SYSTEM
  • INFANTS
  • CHILDREN
  • VACCINE
  • SERUM
  • MOTHERS
  • WOMEN

IgA and Neutralizing Antibodies to Influenza A Virus in Human Milk: A Randomized Trial of Antenatal Influenza Immunization

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Journal Title:

PLoS ONE

Volume:

Volume 8, Number 8

Publisher:

, Pages e70867-e70867

Type of Work:

Article | Final Publisher PDF

Abstract:

Background:Antenatal immunization of mothers with influenza vaccine increases serum antibodies and reduces the rates of influenza illness in mothers and their infants. We report the effect of antenatal immunization on the levels of specific anti-influenza IgA levels in human breast milk. (ClinicalTrials.gov identifier NCT00142389; http://clinicaltrials.gov/ct2/show/NCT00142389). Methods and Findings:The Mother's Gift study was a prospective, blinded, randomized controlled trial that assigned 340 pregnant Bangladeshi mothers to receive either trivalent inactivated influenza vaccine, or 23-valent pneumococcal polysaccharide vaccine during the third trimester. We evaluated breast milk at birth, 6 weeks, 6 months, and 12 months, and serum at 10 weeks and 12 months. Milk and serum specimens from 57 subjects were assayed for specific IgA antibody to influenza A/New Caledonia (H1N1) using an enzyme-linked immunosorbent assay (ELISA) and a virus neutralization assay, and for total IgA using ELISA. Influenza-specific IgA levels in breast milk were significantly higher in influenza vaccinees than in pneumococcal cont rols for at least 6 months postpartum (p = 0.04). Geometric mean concentrations ranged from 8.0 to 91.1 ELISA units/ml in vaccinees, versus 2.3 to 13.7 ELISA units/mL in controls. Virus neutralization titers in milk were 1.2 to 3 fold greater in vaccinees, and correlated with influenza-specific IgA levels (r = 0.86). Greater exclusivity of breastfeeding in the first 6 months of life significantly decreased the expected number of respiratory illness with fever episodes in infants of influenza-vaccinated mothers (p = 0.0042) but not in infants of pneumococcal-vaccinated mothers (p = 0.4154).Conclusions:The sustained high levels of actively produced anti-influenza IgA in breast milk and the decreased infant episodes of respiratory illness with fever suggest that breastfeeding may provide local mucosal protection for the infant for at least 6 months. Studies are needed to determine the cellular and immunologic mechanisms of breast milk-mediated protection after antepartum immunization. Trial Registration: ClinicalTrials.gov NCT00142389.

Copyright information:

© 2013 Schlaudecker et al.

This is an Open Access work distributed under the terms of the Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/).
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