Impact of maternal diphtheria-tetanus-acellular pertussis vaccination on pertussis booster immune responses in toddlers: Follow-up of a randomized trial.


Journal

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

Informations de publication

Date de publication:
12 03 2021
Historique:
received: 09 09 2020
revised: 26 11 2020
accepted: 02 02 2021
pubmed: 23 2 2021
medline: 25 5 2021
entrez: 22 2 2021
Statut: ppublish

Résumé

Transplacentally transferred antibodies induced by maternal pertussis vaccination interfere with infant immune responses to pertussis primary vaccination. We evaluated whether this interference remains in toddlers after booster vaccination. In a prior phase IV, observer-blind, placebo-controlled, randomized study (NCT02377349), pregnant women in Australia, Canada and Europe received intramuscular tetanus-reduced-antigen-content diphtheria-three-component acellular pertussis vaccine (Tdap group) or placebo (control group) at 27 263 (Tdap group) and 277 (control group) toddlers received a DTaP-HepB-IPV/Hib booster. Pre-booster vaccination, observed geometric mean concentrations (GMCs) for the three pertussis antigens and diphtheria were 1.4-1.5-fold higher in controls than in the Tdap group. No differences were observed for the other DTaP-HepB-IPV/Hib antigens. One month post-booster vaccination, booster response rates for pertussis antigens were ≥ 92.1% and seroprotection rates for the other DTaP-HepB-IPV/Hib antigens were ≥ 99.2% in both groups (primary objective). Higher post-booster GMCs were observed in controls versus the Tdap group for anti-filamentous hemagglutinin (1.2-fold), anti-pertussis toxoid (1.5-fold) and anti-diphtheria (1.4-fold). GMCs for the other DTaP-HepB-IPV/Hib antigens were similar between groups. Serious adverse events were reported for three toddlers (controls, not vaccination-related). One death occurred pre-booster (Tdap group, not vaccination-related). As a consequence of interference of maternal pertussis antibodies with infant immune responses to pertussis primary vaccination, pertussis antibody concentrations were still lower in toddlers from Tdap-vaccinated mothers before DTaP-HepB-IPV/Hib booster vaccination. After the booster, antibody concentrations were lower for filamentous hemagglutinin and pertussis toxoid but not for pertactin. The clinical significance of this interference requires further evaluation. ClinicalTrials.gov: NCT02853929.

Sections du résumé

BACKGROUND
Transplacentally transferred antibodies induced by maternal pertussis vaccination interfere with infant immune responses to pertussis primary vaccination. We evaluated whether this interference remains in toddlers after booster vaccination.
METHODS
In a prior phase IV, observer-blind, placebo-controlled, randomized study (NCT02377349), pregnant women in Australia, Canada and Europe received intramuscular tetanus-reduced-antigen-content diphtheria-three-component acellular pertussis vaccine (Tdap group) or placebo (control group) at 27
RESULTS
263 (Tdap group) and 277 (control group) toddlers received a DTaP-HepB-IPV/Hib booster. Pre-booster vaccination, observed geometric mean concentrations (GMCs) for the three pertussis antigens and diphtheria were 1.4-1.5-fold higher in controls than in the Tdap group. No differences were observed for the other DTaP-HepB-IPV/Hib antigens. One month post-booster vaccination, booster response rates for pertussis antigens were ≥ 92.1% and seroprotection rates for the other DTaP-HepB-IPV/Hib antigens were ≥ 99.2% in both groups (primary objective). Higher post-booster GMCs were observed in controls versus the Tdap group for anti-filamentous hemagglutinin (1.2-fold), anti-pertussis toxoid (1.5-fold) and anti-diphtheria (1.4-fold). GMCs for the other DTaP-HepB-IPV/Hib antigens were similar between groups. Serious adverse events were reported for three toddlers (controls, not vaccination-related). One death occurred pre-booster (Tdap group, not vaccination-related).
CONCLUSIONS
As a consequence of interference of maternal pertussis antibodies with infant immune responses to pertussis primary vaccination, pertussis antibody concentrations were still lower in toddlers from Tdap-vaccinated mothers before DTaP-HepB-IPV/Hib booster vaccination. After the booster, antibody concentrations were lower for filamentous hemagglutinin and pertussis toxoid but not for pertactin. The clinical significance of this interference requires further evaluation.
CLINICAL TRIAL REGISTRATION
ClinicalTrials.gov: NCT02853929.

Identifiants

pubmed: 33612341
pii: S0264-410X(21)00130-4
doi: 10.1016/j.vaccine.2021.02.001
pii:
doi:

Substances chimiques

Antibodies, Bacterial 0
Diphtheria-Tetanus-Pertussis Vaccine 0
Diphtheria-Tetanus-acellular Pertussis Vaccines 0
Haemophilus Vaccines 0
Poliovirus Vaccine, Inactivated 0
Vaccines, Combined 0

Banques de données

ClinicalTrials.gov
['NCT02853929']

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1598-1608

Informations de copyright

Copyright © 2021 GlaxoSmithKline Biologicals SA. Published by Elsevier Ltd.. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: BAN reports grants from the GSK group of companies (GSK) and support from other vaccine manufacturers. BC, MAC, NMes, NMey and SOK are employees of GSK, and BC, MAC and NMes own GSK restricted shares. FMT, JGS, SAH, TN and KPP’s institutions received grants from GSK during the conduct of the study. FMT’s institution received financial and non-financial support from Ablynx, Astra Zeneca, GSK, Jansen, MedImmune, MSD, Novavax, Pfizer, Regeneron, Roche, Sanofi Pasteur and Seqirus outside the submitted work. SAH received honoraria for participation in ad-hoc advisory committees for GSK and Sanofi Pasteur. TN received personal fees from GSK for serving as chair of advisory committees outside the submitted work. BT’s institution received grants from GSK during the conduct of the study; research grants for clinical trials were also given to his institution by Pfizer, MSD and Sanofi Pasteur. KPP received a fellowship from National Health and Medical Research Council for conducting the present work, and her institution received financial support from DBV Technologies, Medlmmune, Novavax and Pfizer for conducting trials outside the submitted work. ISC has received grants and/or honoraria as a consultant/advisor or to attend conferences and practical courses from GSK, Sanofi Pasteur, MSD and Pfizer outside the submitted work. JMMA reports receiving fees and non-financial support from GSK, as well as fees from Pfizer and MSD outside the submitted work. LK is working as consultant for GSK. MB, JB, MJCO, EEP, JJ, MMV, PK, PGM, JTRA, SR, ZS, MV, OGV and GVZ declare no conflicts of interest.

Auteurs

Federico Martinón-Torres (F)

Hospital Clínico Universitario de Santiago, Pediatría Clínica, Infectológica y Traslacional, 15706 Santiago de Compostela, Spain; Genetics, Vaccines and Pediatrics Research Group, University of Santiago de Compostela, Instituto de Investigación Sanitaria de Santiago de Compostela, 15706 Santiago de Compostela, Spain.

Scott A Halperin (SA)

Dalhousie University, Canadian Center for Vaccinology, Halifax, NS B3K 6R8, Canada.

Terry Nolan (T)

Murdoch Children's Research Institute, and the Melbourne School of Population and Global Health at The University of Melbourne, Melbourne, VIC 3052, Australia.

Bruce Tapiéro (B)

CHU Sainte Justine, Université de Montréal, Montréal, QC H3T 1C5, Canada.

Kirsten P Perrett (KP)

Murdoch Children's Research Institute, and the Melbourne School of Population and Global Health at The University of Melbourne, Melbourne, VIC 3052, Australia.

Ignacio Salamanca de la Cueva (IS)

Instituto Hispalense de Pediatría, Unidad de Investigación, 41014 Seville, Spain.

José García-Sicilia (J)

Hospital Universitario Madrid Sanchinarro, Servicio de Pediatría, 28050 Madrid, Spain.

Zbynek Stranak (Z)

Institute for the Care of Mother and Child, Neonatology Department, 147 00 Prague, Czech Republic.

Otto G Vanderkooi (OG)

Alberta Children's Hospital, University of Calgary, Departments of Pediatrics, Microbiology, Immunology and Infectious Diseases, Pathology and Laboratory Medicine and Community Health Sciences, Alberta Children's Hospital Research Institute, Alberta, Calgary AB T3B 6A8, Canada.

Pavel Kosina (P)

University Hospital, Department of Infectious Diseases, 500 05 Hradec Kralove, Czech Republic.

Sarka Rumlarova (S)

University Hospital, Department of Infectious Diseases, 500 05 Hradec Kralove, Czech Republic.

Miia Virta (M)

Tampere Vaccine Research Center, Tampere University, 33100 Tampere, Finland.

Jose M Merino Arribas (JMM)

Nuevo Hospital Universitario de Burgos, Departamento de Pediatría, 09006 Burgos, Spain.

Mariano Miranda-Valdivieso (M)

Hospital de Antequera, Servicio de Pediatría, 29200 Antequera, Spain.

Begoña Arias Novas (BA)

Hospital Universitario Sanitas La Zarzuela, Servicio de Pediatría, 28023 Aravaca, Spain.

Jan Bozensky (J)

Vitkovice Hospital, Pediatrics Department, 703 00 Ostrava, Czech Republic.

María José Cilleruelo Ortega (MJC)

Hospital Universitario Puerta de Hierro Majadahonda, Servicio de Pediatría, 28222 Madrid, Spain.

Jose Tomas Ramos Amador (JTR)

Departamento de Salud Pública y Materno-Infantil, Hospital Clínico San Carlos, 28040 Madrid, Spain.

Manuel Baca (M)

Hospital Quiron Malaga, Departamento de Pediatría y Neonatología, 29004 Malaga, Spain.

Esperanza Escribano Palomino (EE)

Hospital Universitario La Paz, Servicio de Neonatologia, 28046 Madrid, Spain.

Gian Vincenzo Zuccotti (GV)

Ospedale dei Bambini Vittore Buzzi, and University of Milan, 20154 Milan, Italy.

Jan Janota (J)

Thomayer Hospital Prague, Department of Neonatology, 140 59 Prague, Czech Republic.

Paola Giovanna Marchisio (PG)

Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico, 20122 Milan, Italy; Università degli Studi di Milano, 20122 Milan, Italy.

Lusine Kostanyan (L)

GSK, Vaccines, 1300 Wavre, Belgium.

Nadia Meyer (N)

GSK, Vaccines, 1300 Wavre, Belgium. Electronic address: nadia.x.meyer@gsk.com.

Maria Angeles Ceregido (MA)

GSK, Vaccines, 1300 Wavre, Belgium.

Brigitte Cheuvart (B)

GSK, Vaccines, 1300 Wavre, Belgium.

Sherine O Kuriyakose (SO)

GSK, Vaccines, Bangalore-560001, India.

Narcisa Mesaros (N)

GSK, Vaccines, 1300 Wavre, Belgium.

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Classifications MeSH