Kinetics of maternally-derived serogroup A, C, Y and W-specific meningococcal immunoglobulin G in Malian women and infants.


Journal

Vaccine
ISSN: 1873-2518
Titre abrégé: Vaccine
Pays: Netherlands
ID NLM: 8406899

Informations de publication

Date de publication:
24 04 2019
Historique:
received: 13 06 2018
revised: 05 03 2019
accepted: 21 03 2019
pubmed: 7 4 2019
medline: 17 9 2020
entrez: 7 4 2019
Statut: ppublish

Résumé

A prospective, randomised, controlled observer-blind trial measuring the efficacy and immunogenicity of trivalent influenza vaccine (TIV) and the immunogenicity of quadrivalent meningococcal conjugate vaccine (MCV) in pregnant women and their infants up to 6 months of age was conducted in Mali. Here we reported the immunogenicity of MCV, which was used as a comparator vaccine to TIV, in this population. Third-trimester pregnant Malian women were randomized to receive TIV or MCV. Blood samples were collected from women prior to vaccination, 28 days post-vaccination, at delivery and 3 and 6 months post-delivery and from infants at birth and 3 and 6 months of age. Meningococcal-specific serogroup (Men) A, C, Y and W-specific antibodies were measured by enzyme linked immunosorbent assay in a randomly selected subset of 50 mother-infant pairs where the mother had received MCV. At birth, 94.0% (47/50) of infants had MenA specific IgG levels ≥ 2 µg/mL decreasing to 72.9% and 30.4% at 3 and 6 months of age. For MenC, 81.3% (39/48) of infants had MenC specific IgG levels ≥ 2 µg/mL at birth decreasing to 29.4% and 17.8% at 3 and 6 months of age. For MenY, 89.6% (43/48) of infants had MenY specific IgG levels ≥ 2 µg/mL at birth decreasing to 64.6% and 62.5% at 3 and 6 months of age. For MenW, 89.6% (43/48) of infants had MenW specific IgG levels ≥ 2 μg/ml at birth decreasing to 62.5% and 41.7% at 3 and 6 months of age. Maternal immunization with MCV conveyed protective levels of IgG at birth through to 3 months of age in the majority of infants.

Identifiants

pubmed: 30952500
pii: S0264-410X(19)30379-2
doi: 10.1016/j.vaccine.2019.03.045
pmc: PMC6990398
pii:
doi:

Substances chimiques

Antibodies, Bacterial 0
Immunoglobulin G 0
Influenza Vaccines 0
Meningococcal Vaccines 0
Vaccines, Conjugate 0

Types de publication

Clinical Trial, Phase IV Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2477-2481

Informations de copyright

Crown Copyright © 2019. Published by Elsevier Ltd. All rights reserved.

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Auteurs

H Findlow (H)

Vaccine Evaluation Unit, Public Health England, Manchester Royal Infirmary, Manchester, UK. Electronic address: helenfindlow@hotmail.com.

M D Tapia (MD)

Center for Vaccine Development, University of Maryland School of Medicine, Baltimore, MD, USA.

S O Sow (SO)

Centre pour le Développement des Vaccins, Bamako, Mali.

F C Haidara (FC)

Centre pour le Développement des Vaccins, Bamako, Mali.

F Coulibaly (F)

Centre pour le Développement des Vaccins, Bamako, Mali.

A M Keita (AM)

Centre pour le Développement des Vaccins, Bamako, Mali.

F Diallo (F)

Centre pour le Développement des Vaccins, Bamako, Mali.

M Doumbia (M)

Centre pour le Développement des Vaccins, Bamako, Mali.

A Traore (A)

Centre pour le Développement des Vaccins, Bamako, Mali.

N Schluterman (N)

Department of Epidemiology, University of Maryland, Baltimore, MD, USA.

D A Clark (DA)

Department of Epidemiology, Emory University Rollins School of Public Health, Atlanta, GA, USA.

R Borrow (R)

Vaccine Evaluation Unit, Public Health England, Manchester Royal Infirmary, Manchester, UK.

M M Levine (MM)

Center for Vaccine Development, University of Maryland School of Medicine, Baltimore, MD, USA.

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Classifications MeSH