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An open-label, phase IV randomised controlled trial of two schedules of a four-component meningococcal B vaccine in UK preterm infants.
Calvert, Anna; Andrews, Nick; Barlow, Sheula; Borrow, Ray; Black, Charlotte; Bromage, Barbara; Carr, Jeremy; Clarke, Paul; Collinson, Andrew C; Few, Karen; Hayward, Naomi; Jones, Christine E; Le Doare, Kirsty; Ladhani, Shamez N; Louth, Jennifer; Papadopoulou, Georgia; Pople, Michelle; Scorrer, Tim; Snape, Matthew D; Heath, Paul T.
Afiliación
  • Calvert A; Centre for Neonatal and Paediatric Infection and Vaccine Institute, St George's, University of London, London, UK acalvert@sgul.ac.uk.
  • Andrews N; St George's University Hospitals NHS Foundation Trust, London, UK.
  • Barlow S; Immunisation and Vaccine Preventable Diseases Division, UK Health Security Agency, London, UK.
  • Borrow R; Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
  • Black C; Vaccine Evaluation Unit, UK Health Security Agency, Manchester Royal Infirmary, Manchester, UK.
  • Bromage B; Oxford Vaccine Group, Department of Paediatrics, University of Oxford, Oxford, UK.
  • Carr J; Royal Cornwall Hospitals NHS Trust, Truro, Cornwall, UK.
  • Clarke P; Oxford Vaccine Group, Department of Paediatrics, University of Oxford, Oxford, UK.
  • Collinson AC; Monash University, Clayton, Victoria, Australia.
  • Few K; Neonatal Intensive Care Unit, Norfolk and Norwich University Hospital NHS Trust, Norwich, UK.
  • Hayward N; Norwich Medical School, University of East Anglia, Norwich, UK.
  • Jones CE; Royal Cornwall Hospitals NHS Trust, Truro, Cornwall, UK.
  • Le Doare K; Neonatal Intensive Care Unit, Norfolk and Norwich University Hospital NHS Trust, Norwich, UK.
  • Ladhani SN; Centre for Neonatal and Paediatric Infection and Vaccine Institute, St George's, University of London, London, UK.
  • Louth J; St George's University Hospitals NHS Foundation Trust, London, UK.
  • Papadopoulou G; Faculty of Medicine and Institute for Life Sciences, University of Southampton, Southampton, UK.
  • Pople M; NIHR Southampton Clinical Research Facility and NIHR Southampton Biomedical Research Centre, University Hospital Southampton NHS Foundation Trust, Southampton, UK.
  • Scorrer T; Centre for Neonatal and Paediatric Infection and Vaccine Institute, St George's, University of London, London, UK.
  • Snape MD; Makerere University Johns Hopkins University, Kampala, Uganda.
  • Heath PT; Pathogen Immunology Group, UK Health Security Agency, Salisbury, UK.
Arch Dis Child ; 2024 Jul 08.
Article en En | MEDLINE | ID: mdl-38977298
ABSTRACT

OBJECTIVE:

To compare immunological responses of preterm infants to a four-component meningococcal B vaccine (4CMenB; Bexsero) following a 2+1 vs a 3+1 schedule, and to describe reactogenicity of routine vaccines.

DESIGN:

An open-label, phase IV randomised study conducted across six UK sites.

SETTING:

Neonatal units, postnatal wards, community recruitment following discharge.

PARTICIPANTS:

129 preterm infants born at a gestation of <35 weeks (64 in group 1 (2+1), 65 in group 2 (3+1)) were included in the analysis. Analysis was completed for postprimary samples from 125 participants (59 in group 1, 66 in group 2) and for postbooster samples from 118 participants (59 in both groups).

INTERVENTIONS:

Infants randomised to 4CMenB according to a 2+1 or a 3+1 schedule, alongside routine vaccines. MAIN OUTCOME

MEASURES:

Serum bactericidal antibody (SBA) assays performed at 5, 12 and 13 months of age geometric mean titres (GMTs) and proportions of infants achieving titres ≥4 compared between groups.

RESULTS:

There were no significant differences in SBA GMTs between infants receiving a 2+1 compared with a 3+1 schedule following primary or booster vaccination, but a significantly higher proportion of infants had an SBA titre ≥4 against strain NZ98/254 (porin A) at 1 month after primary vaccination using a 3+1 compared with a 2+1 schedule (3+1 87% (95% CI 76 to 94%), 2+1 70% (95% CI 56 to 81%), p=0.03).At 12 weeks of age those in the 3+1 group, who received a dose of 4CMenB, had significantly more episodes of fever >38.0°C than those in the 2+1 group who did not (group 2+1 2% (n=1); 3+1 14% (n=9); p=0.02).

CONCLUSIONS:

Both schedules were immunogenic in preterm infants, although a lower response against strain NZ98/254 was seen in the 2+1 schedule; ongoing disease surveillance is important in understanding the clinical significance of this difference. TRIAL REGISTRATION NUMBER NCT03125616.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Arch Dis Child Año: 2024 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Arch Dis Child Año: 2024 Tipo del documento: Article País de afiliación: Reino Unido
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