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Boosting Teenagers With Acellular Pertussis Vaccines Containing Recombinant or Chemically Inactivated Pertussis Toxin: A Randomized Clinical Trial.
Blanchard Rohner, Geraldine; Chatzis, Olga; Chinwangso, Pailinrut; Rohr, Marie; Grillet, Stéphane; Salomon, Carole; Lemaître, Barbara; Boonrak, Pitchaya; Lawpoolsri, Saranath; Clutterbuck, Elizabeth; Poredi, Indrajeet Kumar; Wijagkanalan, Wassana; Spiegel, Jane; Pham, Hong Thai; Viviani, Simonetta; Siegrist, Claire-Anne.
Affiliation
  • Blanchard Rohner G; Department of Paediatrics, Children's Hospital of Geneva, University Hospitals of Geneva.
  • Chatzis O; Center for Vaccinology and Neonatal Immunology, Department of Pediatrics and Pathology-Immunology, Medical Faculty and University Hospitals of Geneva, Switzerland.
  • Chinwangso P; Department of Paediatrics, Children's Hospital of Geneva, University Hospitals of Geneva.
  • Rohr M; Center for Vaccinology and Neonatal Immunology, Department of Pediatrics and Pathology-Immunology, Medical Faculty and University Hospitals of Geneva, Switzerland.
  • Grillet S; BioNet-Asia Co, Ltd, Bangkok, Thailand.
  • Salomon C; Department of Paediatrics, Children's Hospital of Geneva, University Hospitals of Geneva.
  • Lemaître B; Center for Vaccinology and Neonatal Immunology, Department of Pediatrics and Pathology-Immunology, Medical Faculty and University Hospitals of Geneva, Switzerland.
  • Boonrak P; Center for Vaccinology and Neonatal Immunology, Department of Pediatrics and Pathology-Immunology, Medical Faculty and University Hospitals of Geneva, Switzerland.
  • Lawpoolsri S; Department of Paediatrics, Children's Hospital of Geneva, University Hospitals of Geneva.
  • Clutterbuck E; Laboratory of Vaccinology, University Hospitals of Geneva, Switzerland.
  • Poredi IK; Center of Excellence for Biomedical and Public Health Informatics, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
  • Wijagkanalan W; Center of Excellence for Biomedical and Public Health Informatics, Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
  • Spiegel J; Oxford Vaccine Group, Department of Paediatrics, University of Oxford.
  • Pham HT; National Institute for Health Research Oxford Biomedical Research Centre, United Kingdom.
  • Viviani S; BioNet-Asia Co, Ltd, Bangkok, Thailand.
  • Siegrist CA; BioNet-Asia Co, Ltd, Bangkok, Thailand.
Clin Infect Dis ; 68(7): 1213-1222, 2019 03 19.
Article in En | MEDLINE | ID: mdl-30759183
ABSTRACT

BACKGROUND:

Protection induced by acellular pertussis (aP) vaccines is partial and short-lived, especially in teenagers, calling for novel immunization strategies.

METHODS:

We conducted an investigator-driven proof-of-concept randomized controlled trial in aP-primed adolescents in Geneva to assess the immunogenicity and reactogenicity of a novel recombinant aP (r-aP) vaccine including recombinant pertussis toxin (PT) and filamentous hemagglutinin (FHA) coadministered with tetanus-diphtheria toxoids (Td), compared to a licensed tetanus-diphtheria-aP vaccine containing chemically detoxified PT (cd/Tdap). The primary immunological endpoints were day 28/365 geometric mean concentrations (GMCs) of total and neutralizing anti-PT antibodies. Memory B cells were assessed.

RESULTS:

Sixty-two aP-primed adolescents were randomized and vaccinated with r-aP + Td or cd/Tdap. Reactogenicity, adverse events, and baseline GMCs were similar between the groups. Day 28 PT-neutralizing GMCs were low after cd/Tdap (73.91 [95% confidence interval {CI}, 49.88-109.52] IU/mL) and approximately 2-fold higher after r-aP + Td (127.68 [95% CI, 96.73-168.53] IU/mL; P = .0162). Anti-PT GMCs were also low after cd/Tdap (52.43 [95% CI, 36.41-75.50] IU/mL) and 2-fold higher after r-aP + Td (113.74 [95% CI, 88.31-146.50] IU/mL; P = .0006). Day 28 anti-FHA GMCs were similar in both groups. Day 365 anti-PT (but not PT-neutralizing) GMCs remained higher in r-aP + Td vaccinees. PT-specific memory B cells increased significantly after r-aP + Td but not cd/Tdap boosting.

CONCLUSIONS:

Boosting aP-primed adolescents with r-aP induced higher anti-PT and PT-neutralizing responses than cd/Tdap and increased PT-specific memory B cells. Despite this superior immunogenicity, r-aP may have to be given repeatedly, earlier, and/or with novel adjuvants to exert an optimal influence in aP-primed subjects. CLINICAL TRIALS REGISTRATION NCT02946190.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pertussis Vaccine / Whooping Cough / Immunization, Secondary / Pertussis Toxin / Antibodies, Neutralizing Type of study: Clinical_trials Limits: Adolescent / Child / Female / Humans / Male Country/Region as subject: Europa Language: En Journal: Clin Infect Dis Journal subject: DOENCAS TRANSMISSIVEIS Year: 2019 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pertussis Vaccine / Whooping Cough / Immunization, Secondary / Pertussis Toxin / Antibodies, Neutralizing Type of study: Clinical_trials Limits: Adolescent / Child / Female / Humans / Male Country/Region as subject: Europa Language: En Journal: Clin Infect Dis Journal subject: DOENCAS TRANSMISSIVEIS Year: 2019 Type: Article