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Pneumococcal carriage following PCV13 delivered as one primary and one booster dose (1 + 1) compared to two primary doses and a booster (2 + 1) in UK infants.
Goldblatt, David; Andrews, Nick J; Sheppard, Carmen L; Rose, Samuel; Aley, Parvinder K; Roalfe, Lucy; Southern, Jo; Robinson, Hannah; Pearce, Emma; Plested, Emma; Johnson, Marina; Litt, David J; Fry, Norman K; Waight, Pauline; Snape, Matthew D; Miller, Elizabeth.
Afiliación
  • Goldblatt D; Infection, Immunity and Inflammation Department, UCL Great Ormond Street Institute of Child Health Biomedical Research Centre, London, United Kingdom. Electronic address: d.goldblatt@ucl.ac.uk.
  • Andrews NJ; Immunisation and Vaccine Preventable Diseases, UK Health Security Agency, United Kingdom.
  • Sheppard CL; Respiratory and Vaccine Preventable Bacteria Reference Unit, UK Health Security Agency, London Vaccine Preventable Bacteria Section, National Infection Service Public Health England Colindale, United Kingdom.
  • Rose S; Respiratory and Vaccine Preventable Bacteria Reference Unit, UK Health Security Agency, London Vaccine Preventable Bacteria Section, National Infection Service Public Health England Colindale, United Kingdom.
  • Aley PK; Oxford Vaccine Group, Department of Paediatrics, University of Oxford, Oxford, United Kingdom and NIHR Oxford Biomedical Research Centre, United Kingdom.
  • Roalfe L; Infection, Immunity and Inflammation Department, UCL Great Ormond Street Institute of Child Health Biomedical Research Centre, London, United Kingdom.
  • Southern J; Immunisation and Vaccine Preventable Diseases, UK Health Security Agency, United Kingdom.
  • Robinson H; Oxford Vaccine Group, Department of Paediatrics, University of Oxford, Oxford, United Kingdom and NIHR Oxford Biomedical Research Centre, United Kingdom.
  • Pearce E; Infection, Immunity and Inflammation Department, UCL Great Ormond Street Institute of Child Health Biomedical Research Centre, London, United Kingdom.
  • Plested E; Oxford Vaccine Group, Department of Paediatrics, University of Oxford, Oxford, United Kingdom and NIHR Oxford Biomedical Research Centre, United Kingdom.
  • Johnson M; Infection, Immunity and Inflammation Department, UCL Great Ormond Street Institute of Child Health Biomedical Research Centre, London, United Kingdom.
  • Litt DJ; Respiratory and Vaccine Preventable Bacteria Reference Unit, UK Health Security Agency, London Vaccine Preventable Bacteria Section, National Infection Service Public Health England Colindale, United Kingdom.
  • Fry NK; Immunisation and Vaccine Preventable Diseases, UK Health Security Agency, United Kingdom.
  • Waight P; Infection, Immunity and Inflammation Department, UCL Great Ormond Street Institute of Child Health Biomedical Research Centre, London, United Kingdom.
  • Snape MD; Oxford Vaccine Group, Department of Paediatrics, University of Oxford, Oxford, United Kingdom and NIHR Oxford Biomedical Research Centre, United Kingdom.
  • Miller E; Department of Infectious Disease Epidemiology, London School of Hygiene and Tropical Medicine, United Kingdom.
Vaccine ; 41(19): 3019-3023, 2023 05 05.
Article en En | MEDLINE | ID: mdl-37045683
ABSTRACT
In January 2020 the UK changed from a 2 + 1 schedule for 13-valent pneumococcal conjugate vaccine (PCV13) to a 1 + 1 schedule (doses at 3 and 12 months) based on a randomized immunogenicity trial comparing the two schedules. Carriage prevalence measured at the time of booster and 6 months later in 191 of the 213 study infants was 57 % (109/191) and 60 % (114/190) respectively. There were eight episodes of vaccine-type (VT) or vaccine-related 6C carriage in the 2 + 1 and six in the 1 + 1 group; ≥4-fold rises in serotype-specific IgG in 71 children with paired post-booster and follow up blood samples at 21-33 months of age were found in 20 % (7/35) of the 2 + 1 and 15 % (6/41) of the 1 + 1 group. VTs identified in carriage and inferred from serology were similar comprising 3, 19A and 19F. Dropping a priming dose from the 2 + 1 PCV 13 schedule did not increase VT carriage in the study cohort. Ongoing population level carriage studies will be important to confirm this.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Infecciones Neumocócicas Tipo de estudio: Clinical_trials / Risk_factors_studies Límite: Child / Humans / Infant País/Región como asunto: Europa Idioma: En Revista: Vaccine Año: 2023 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Infecciones Neumocócicas Tipo de estudio: Clinical_trials / Risk_factors_studies Límite: Child / Humans / Infant País/Región como asunto: Europa Idioma: En Revista: Vaccine Año: 2023 Tipo del documento: Article