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Immunogenicity, transplacental transfer of pertussis antibodies and safety following pertussis immunization during pregnancy: Evidence from a randomized, placebo-controlled trial

Authors :
Federico Martinón-Torres
Paola Marchisio
Manuel Marcos Fernández
Cristina Martínez Pancorbo
Pavel Kosina
Juan Eloy Asenjo de la Fuente
Maria Angeles Ceregido
Brigitte Cheuvart
Yolanda Romero Espinar
Terry Nolan
María de la Calle Fernández-Miranda
miguel angel rodriguez zambrano
Lusine Kostanyan
Z Stranak
Nadia Meyer
Sherine Kuriyakose
Miia Virta
Scott A. Halperin
Bruce Tapiero
Adrián Martín García
Narcisa Mesaros
Maria Dolores Camacho Marín
Gian Vincenzo Zuccotti
Maria Begoña Encinas Pardilla
Kirsten P Perrett
Paolo Manzoni
Otto G. Vanderkooi
Ignacio Cristobal García
UAM. Departamento de Obstetricia y Ginecología
Source :
Biblos-e Archivo: Repositorio Institucional de la UAM, Universidad Autónoma de Madrid, DDFV. Repositorio Institucional de la Universidad Francisco de Vitoria, instname, Biblos-e Archivo. Repositorio Institucional de la UAM, DDFV: Repositorio Institucional de la Universidad Francisco de Vitoria, Universidad Francisco de Vitoria
Publication Year :
2019

Abstract

Background: Pertussis immunization during pregnancy is recommended in many countries. Data from large randomized controlled trials are needed to assess the immunogenicity, reactogenicity and safety of this approach. Methods: This phase IV, observer-blind, randomized, placebo-controlled, multicenter trial assessed immunogenicity, transplacental transfer of maternal pertussis antibodies, reactogenicity and safety of a reduced-antigen-content diphtheria-tetanus-three-component acellular pertussis vaccine (Tdap) during pregnancy. Women received Tdap or placebo at 27–36 weeks’ gestation with crossover ≤ 72-hour-postpartum immunization. Immune responses were assessed before the pregnancy dose and 1 month after, and from the umbilical cord at delivery. Superiority (primary objective) was reached if the lower limits of the 95% confidence intervals (CIs) of the pertussis geometric mean concentration (GMC) ratios (Tdap/control) in cord blood were ≥ 1.5. Solicited and unsolicited adverse events (AEs) and pregnancy-/neonate-related AEs of interest were recorded. Results: 687 pregnant women were vaccinated (Tdap: N = 341 control: N = 346). Superiority of the pertussis immune response (maternally transferred pertussis antibodies in cord blood) was demonstrated by the GMC ratios (Tdap/control): 16.1 (95% CI: 13.5–19.2) for anti-filamentous hemagglutinin, 20.7 (15.9–26.9) for anti-pertactin and 8.5 (7.0–10.2) for anti-pertussis toxoid. Rates of pregnancy-/neonate-related AEs of interest, solicited general and unsolicited AEs were similar between groups. None of the serious AEs reported throughout the study were considered related to maternal Tdap vaccination. Conclusions: Tdap vaccination during pregnancy resulted in high levels of pertussis antibodies in cord blood, was well tolerated and had an acceptable safety profile. This supports the recommendation of Tdap vaccination during pregnancy to prevent early-infant pertussis disease. Clinical Trial Registration. ClinicalTrials.gov: NCT02377349.<br />This work was supported by GlaxoSmithKline Biologicals S.A.

Details

ISSN :
18732518 and 02377349
Volume :
38
Issue :
8
Database :
OpenAIRE
Journal :
Vaccine
Accession number :
edsair.doi.dedup.....8e1f1d928d4e30996d0aa44646a90c87