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

Author:

Leroux-Roels Geert1,Bebia Zourab2,Maes Cathy1,Aerssens Annelies1,De Boever Fien1,Grassano Luca3,Buffi Giada3,Margarit Immaculada3,Karsten Annette4,Cho Stephen56,Slobod Karen56,Corsaro Bartholomew2,Henry Ouzama2

Affiliation:

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

2. GlaxoSmithKline (GSK), Rockville, Maryland

3. GSK, Siena, Italy

4. GSK, Marburg, Germany

5. Novartis, Cambridge, Massachusetts

6. GSK, Cambridge, Massachusetts

Abstract

Abstract 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

Funder

Novartis Vaccines Division and GlaxoSmithKline Biologicals SA

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

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