4.7 Article

The Effect of Maternal Pertussis Immunization on Infant Vaccine Responses to a Booster Pertussis-Containing Vaccine in Vietnam

Journal

CLINICAL INFECTIOUS DISEASES
Volume 63, Issue -, Pages S197-S204

Publisher

OXFORD UNIV PRESS INC
DOI: 10.1093/cid/ciw551

Keywords

pertussis; vaccination in pregnancy; maternal antibodies

Funding

  1. VLIR-UOS (Flemish Interuniversity Council) [ZEIN2012Z131]
  2. Fund for Scientific Research-Flanders (FWO) [G.A032.12N]
  3. National Foundation for Science and Technology Development-NAFOSTED [FWO.2011.03]
  4. Antwerp Study Centre for Infectious Diseases (ASCID)
  5. FWO [FWO 12D6114N]
  6. University of Antwerp scientific chair in Evidence-Based Vaccinology - Pfizer
  7. BELSPO (Federal Service Science Policy)
  8. Belgian Ministry of Social Affairs within the Health Insurance System

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Background. Maternal vaccination with an acellular pertussis (aP)-containing vaccine is a recommended strategy in a growing number of industrialized countries, to protect young infants from disease. Little is known on the effect of this strategy in low-and middle-income countries. Following a previous report on the effect of adding a pertussis and diphtheria component to the tetanus vaccination program in pregnant women in Vietnam, we report on infant immune responses to a booster aP vaccine dose in this randomized controlled clinical trial. Methods. Thirty infants of Tdap (tetanus, diphtheria, and acellular pertussis)-vaccinated pregnant women and 37 infants of women vaccinated with a tetanus-only vaccine received a fourth aP-containing vaccine dose in the second year of life. Blood was taken 1 month after the fourth infant dose. Immunoglobulin G (IgG) antibodies against pertussis toxin (PT), filamentous hemagglutinin (FHA), pertactin (Prn), tetanus toxoid (TT), and diphtheria toxoid (DT) were measured using commercially available enzyme-linked immunosorbent assays (ELISA). Results. One month after the booster dose, significantly lower antibody titers were measured in the Tdap group for anti-TT IgG (P < .001) only. Anti-DT IgG, anti-PT IgG, anti-Prn IgG, and anti-FHA IgG antibody titers were comparable for both groups. A rise in antibody concentrations was elicited for all (except DT) antigens after boosting. Conclusions. The present results indicate that the blunting of infant pertussis responses induced by maternal immunization, measured after a primary series of aP vaccines, was resolved with the booster aP vaccine dose. These results add to the evidence for national and international decision makers on maternal immunization as a vaccination strategy for protection of young infants against infectious diseases.

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