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Immunogenicity, transplacental transfer of pertussis antibodies and safety following pertussis immunization during pregnancy: Evidence from a randomized, placebo-controlled trial
- 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.
- Subjects :
- Pediatrics
medicine.medical_specialty
Medicina
Whooping Cough
030231 tropical medicine
Adult formulation acellular pertussis vaccine
Maternal immunization
Tdap
Antibodies, Bacterial
Diphtheria-Tetanus-acellular Pertussis Vaccines
Female
Humans
Infant, Newborn
Pregnancy
Single-Blind Method
Vaccination
Immunity, Maternally-Acquired
Maternal Exposure
Antibodies
Maternally-Acquired
03 medical and health sciences
0302 clinical medicine
Medicine
030212 general & internal medicine
Whooping cough
Reactogenicity
General Veterinary
General Immunology and Microbiology
business.industry
Tetanus
Diphtheria
Bacterial
Immunity
Public Health, Environmental and Occupational Health
Toxoid
Infant
Newborn
medicine.disease
Infectious Diseases
Molecular Medicine
business
Subjects
Details
- ISSN :
- 18732518 and 02377349
- Volume :
- 38
- Issue :
- 8
- Database :
- OpenAIRE
- Journal :
- Vaccine
- Accession number :
- edsair.doi.dedup.....8e1f1d928d4e30996d0aa44646a90c87