Ten-Year Antibody Persistence and Booster Response to MenACWY-TT Vaccine After Primary Vaccination at 1-10 Years of Age.


Journal

Human vaccines & immunotherapeutics
ISSN: 2164-554X
Titre abrégé: Hum Vaccin Immunother
Pays: United States
ID NLM: 101572652

Informations de publication

Date de publication:
02 06 2020
Historique:
entrez: 30 6 2020
pubmed: 1 7 2020
medline: 22 6 2021
Statut: ppublish

Résumé

This phase 3B, open-label, extension study (NCT01962207) evaluated long-term persistence of antibodies induced by the quadrivalent meningococcal vaccine conjugated to tetanus toxoid (MenACWY-TT) compared with the meningococcal serogroup C vaccine conjugated to CRM (MenC-CRM) and the quadrivalent meningococcal polysaccharide vaccine (MenACWY-PS) 6 to 10 y after primary vaccination in toddlers (aged 1-<2 y; MenACWY-TT and MenC-CRM) and children (aged 2-<11 y; MenACWY-TT and MenACWY-PS). Antibody responses against meningococcal serogroups A, C, W, and Y were assessed by serum bactericidal antibody assays using rabbit (rSBA) or human (hSBA) complement. A MenACWY-TT booster dose at Year 10 was given to all eligible subjects regardless of the primary vaccine received. At Year 10, the percentages of subjects with rSBA titers ≥1:8 for serogroups A, C, W, and Y were as follows: MenACWY-TT (toddlers), 65.6%, 82.8%, 31.3%, 43.8%, respectively; MenC-CRM, 88.2% for serogroup C; MenACWY-TT (children), 88.9%, 84.1%, 67.1%, 65.9%; and MenACWY-PS, 28.6%, 81.0%, 23.8%, and 23.8%. Corresponding percentages for hSBA titers ≥1:4 were as follows: MenACWY-TT (toddlers), 31.1%, 91.9%, 44.4%, 41.4%; MenC-CRM, 93.8% for serogroup C; MenACWY-TT (children), 34.8%, 91.1%, 61.2%, 72.6%; and MenACWY-PS, 33.3%, 100.0%, 26.3%, and 44.4%. One month after the MenACWY-TT booster, the percentage of subjects with vaccine response ranged from 75.7% to 100.0% across serogroups in all study groups. Postbooster vaccine responses were generally comparable between groups across serogroups. No new safety signals were identified. Antibody responses persisted 10 y after MenACWY-TT vaccination. The MenACWY-TT booster dose was well tolerated and elicited robust immune responses.

Identifiants

pubmed: 32598244
doi: 10.1080/21645515.2020.1746110
pmc: PMC7482884
doi:

Substances chimiques

Antibodies, Bacterial 0
Meningococcal Vaccines 0
Vaccines, Conjugate 0
tetravalent meningococcal serogroups A, C, W-135 and Y tetanus toxoid conjugate vaccine 0

Banques de données

ClinicalTrials.gov
['NCT01962207']

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1280-1291

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Auteurs

Timo Vesikari (T)

Nordic Research Network Ltd , Tampere, Finland.

Paula Peyrani (P)

Pfizer Vaccine Clinical Research and Development, Pfizer Inc , Collegeville, PA, USA.

Chris Webber (C)

Pfizer Vaccine Clinical Research and Development, Pfizer Ltd , Hurley, Berkshire, UK.

Marie Van Der Wielen (M)

Global Vaccines Research and Development, GlaxoSmithKline , Wavre, Belgium.

Brigitte Cheuvart (B)

Global Vaccines Research and Development, GlaxoSmithKline , Wavre, Belgium.

Nathalie De Schrevel (N)

Global Vaccines Research and Development, GlaxoSmithKline , Rixensart, Belgium.

Emmanuel Aris (E)

Global Vaccines Research and Development, GlaxoSmithKline , Wavre, Belgium.

Mark Cutler (M)

Pfizer Vaccine Research and Development, Pfizer Inc , Pearl River, NY, USA.

Ping Li (P)

Pfizer Vaccine Clinical Research and Development, Pfizer Inc , Collegeville, PA, USA.

John L Perez (JL)

Pfizer Vaccine Clinical Research and Development, Pfizer Inc , Collegeville, PA, USA.

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Classifications MeSH