Safety and Immunogenicity of a Second Dose of an Investigational Maternal Trivalent Group B Streptococcus Vaccine in Nonpregnant Women 4-6 Years After a First Dose: Results From a Phase 2 Trial.


Journal

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
ISSN: 1537-6591
Titre abrégé: Clin Infect Dis
Pays: United States
ID NLM: 9203213

Informations de publication

Date de publication:
10 06 2020
Historique:
received: 28 02 2019
accepted: 09 08 2019
pubmed: 9 8 2019
medline: 7 1 2021
entrez: 9 8 2019
Statut: ppublish

Résumé

Maternal immunization against group B streptococcus (GBS) could protect infants from invasive GBS disease. Additional doses in subsequent pregnancies may be needed. We evaluated the safety and immunogenicity of a second dose of an investigational trivalent CRM197-glycoconjugate GBS vaccine (targeting serotypes Ia/Ib/III), administered to nonpregnant women 4-6 years postdose 1. Healthy women either previously vaccinated with 1 dose of trivalent GBS vaccine 4-6 years before enrollment (n = 53) or never GBS vaccinated (n = 27) received a single trivalent GBS vaccine injection. Adverse events (AEs) were recorded. Serotype-specific (Ia/Ib/III) anti-GBS antibodies were measured by multiplex immunoassay prevaccination and 30/60 days postvaccination. AEs were reported with similar rates after a first or second dose; none were serious. Of previously GBS-vaccinated women, 92%-98% had anti-GBS concentrations that exceeded an arbitrary threshold (8 µg/mL) for each serotype 60 days postdose 2 vs 36%-56% postdose 1 in previously non-GBS-vaccinated women. Of previously GBS-vaccinated women with undetectable baseline (predose 1) anti-GBS levels, 90%-98% reached this threshold postdose 2. For each serotype, anti-GBS geometric mean concentrations (GMCs) 30/60 days postdose 2 in previously GBS-vaccinated women were ≥200-fold higher than baseline GMCs. Among women with undetectable baseline anti-GBS levels, postdose 2 GMCs in previously GBS-vaccinated women exceeded postdose 1 GMCs in previously non-GBS-vaccinated women (≥7-fold). A second trivalent GBS vaccine dose administered 4-6 years postdose 1 was immunogenic with a favorable safety profile. Women with undetectable preexisting anti-GBS concentrations may benefit from a sufficiently spaced second vaccine dose. NCT02690181.

Sections du résumé

BACKGROUND
Maternal immunization against group B streptococcus (GBS) could protect infants from invasive GBS disease. Additional doses in subsequent pregnancies may be needed. We evaluated the safety and immunogenicity of a second dose of an investigational trivalent CRM197-glycoconjugate GBS vaccine (targeting serotypes Ia/Ib/III), administered to nonpregnant women 4-6 years postdose 1.
METHODS
Healthy women either previously vaccinated with 1 dose of trivalent GBS vaccine 4-6 years before enrollment (n = 53) or never GBS vaccinated (n = 27) received a single trivalent GBS vaccine injection. Adverse events (AEs) were recorded. Serotype-specific (Ia/Ib/III) anti-GBS antibodies were measured by multiplex immunoassay prevaccination and 30/60 days postvaccination.
RESULTS
AEs were reported with similar rates after a first or second dose; none were serious. Of previously GBS-vaccinated women, 92%-98% had anti-GBS concentrations that exceeded an arbitrary threshold (8 µg/mL) for each serotype 60 days postdose 2 vs 36%-56% postdose 1 in previously non-GBS-vaccinated women. Of previously GBS-vaccinated women with undetectable baseline (predose 1) anti-GBS levels, 90%-98% reached this threshold postdose 2. For each serotype, anti-GBS geometric mean concentrations (GMCs) 30/60 days postdose 2 in previously GBS-vaccinated women were ≥200-fold higher than baseline GMCs. Among women with undetectable baseline anti-GBS levels, postdose 2 GMCs in previously GBS-vaccinated women exceeded postdose 1 GMCs in previously non-GBS-vaccinated women (≥7-fold).
CONCLUSIONS
A second trivalent GBS vaccine dose administered 4-6 years postdose 1 was immunogenic with a favorable safety profile. Women with undetectable preexisting anti-GBS concentrations may benefit from a sufficiently spaced second vaccine dose.
CLINICAL TRIALS REGISTRATION
NCT02690181.

Identifiants

pubmed: 31394574
pii: 5545276
doi: 10.1093/cid/ciz737
pmc: PMC7286364
doi:

Substances chimiques

Antibodies, Bacterial 0
Streptococcal Vaccines 0
Vaccines, Conjugate 0

Banques de données

ClinicalTrials.gov
['NCT02690181']

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

2570-2579

Commentaires et corrections

Type : CommentIn

Informations de copyright

© The Author(s) 2019. Published by Oxford University Press for the Infectious Diseases Society of America.

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Auteurs

Geert Leroux-Roels (G)

Center for Vaccinology, Ghent University and Ghent University Hospital, Belgium.

Zourab Bebia (Z)

GlaxoSmithKline (GSK), Rockville, Maryland.

Cathy Maes (C)

Center for Vaccinology, Ghent University and Ghent University Hospital, Belgium.

Annelies Aerssens (A)

Center for Vaccinology, Ghent University and Ghent University Hospital, Belgium.

Fien De Boever (F)

Center for Vaccinology, Ghent University and Ghent University Hospital, Belgium.

Luca Grassano (L)

GSK, Siena, Italy.

Giada Buffi (G)

GSK, Siena, Italy.

Immaculada Margarit (I)

GSK, Siena, Italy.

Annette Karsten (A)

GSK, Marburg, Germany.

Stephen Cho (S)

Novartis, Cambridge, Massachusetts.
GSK, Cambridge, Massachusetts.

Karen Slobod (K)

Novartis, Cambridge, Massachusetts.
GSK, Cambridge, Massachusetts.

Bartholomew Corsaro (B)

GlaxoSmithKline (GSK), Rockville, Maryland.

Ouzama Henry (O)

GlaxoSmithKline (GSK), Rockville, Maryland.

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