The predicted persistence and kinetics of antibody decline 9years after pre-school booster vaccination in UK children

Long term follow-up of vaccine trials is essential to establish the duration of protection. In the context of worldwide concern about rising pertussis incidence, estimates of antibody persistence after vaccination, which do not account for the rise in antibody due to natural boosting or infection, m...

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Veröffentlicht in:Vaccine 2016-07, Vol.34 (35), p.4221-4228
Hauptverfasser: Voysey, Merryn, Kandasamy, Rama, Yu, Ly-Mee, Baudin, Martine, Sadorge, Christine, Thomas, Stéphane, John, Tessa, Pollard, Andrew J.
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container_end_page 4228
container_issue 35
container_start_page 4221
container_title Vaccine
container_volume 34
creator Voysey, Merryn
Kandasamy, Rama
Yu, Ly-Mee
Baudin, Martine
Sadorge, Christine
Thomas, Stéphane
John, Tessa
Pollard, Andrew J.
description Long term follow-up of vaccine trials is essential to establish the duration of protection. In the context of worldwide concern about rising pertussis incidence, estimates of antibody persistence after vaccination, which do not account for the rise in antibody due to natural boosting or infection, may overestimate the degree of protection afforded by pertussis vaccines. This was a 5year follow up study of a randomised controlled trial of diphtheria, tetanus, pertussis and polio booster vaccines in UK children aged 3.5–5years. Antibody persistence was measured at 1month, 1, 3, and 5years after vaccination and the kinetics of antibody decline were modelled longitudinally. Estimates of predicted antibody persistence 9years after the pre-school booster were derived from model parameters. Antibody levels 9years after vaccination were predicted to be above accepted thresholds for protection for diphtheria, tetanus and polio. Antibody responses to pertussis toxoid were undetectable in 49% of children at the 5year follow up visit, and responses were predicted to be undetectable in 69% (95% CI 45–88%) of children by the time of their teenage booster at 13–14years of age. There is no defined correlate of protection for pertussis. However, the large proportion of participants in this study with undetectable pertussis antibody levels at both measured and predicted timepoints suggests sub-optimal immunity in adolescence. Adding pertussis to the teenage booster for UK children as is done in other countries, would enhance immunity in adolescence.
doi_str_mv 10.1016/j.vaccine.2016.06.051
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In the context of worldwide concern about rising pertussis incidence, estimates of antibody persistence after vaccination, which do not account for the rise in antibody due to natural boosting or infection, may overestimate the degree of protection afforded by pertussis vaccines. This was a 5year follow up study of a randomised controlled trial of diphtheria, tetanus, pertussis and polio booster vaccines in UK children aged 3.5–5years. Antibody persistence was measured at 1month, 1, 3, and 5years after vaccination and the kinetics of antibody decline were modelled longitudinally. Estimates of predicted antibody persistence 9years after the pre-school booster were derived from model parameters. Antibody levels 9years after vaccination were predicted to be above accepted thresholds for protection for diphtheria, tetanus and polio. Antibody responses to pertussis toxoid were undetectable in 49% of children at the 5year follow up visit, and responses were predicted to be undetectable in 69% (95% CI 45–88%) of children by the time of their teenage booster at 13–14years of age. There is no defined correlate of protection for pertussis. However, the large proportion of participants in this study with undetectable pertussis antibody levels at both measured and predicted timepoints suggests sub-optimal immunity in adolescence. 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In the context of worldwide concern about rising pertussis incidence, estimates of antibody persistence after vaccination, which do not account for the rise in antibody due to natural boosting or infection, may overestimate the degree of protection afforded by pertussis vaccines. This was a 5year follow up study of a randomised controlled trial of diphtheria, tetanus, pertussis and polio booster vaccines in UK children aged 3.5–5years. Antibody persistence was measured at 1month, 1, 3, and 5years after vaccination and the kinetics of antibody decline were modelled longitudinally. Estimates of predicted antibody persistence 9years after the pre-school booster were derived from model parameters. Antibody levels 9years after vaccination were predicted to be above accepted thresholds for protection for diphtheria, tetanus and polio. 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Antibody responses to pertussis toxoid were undetectable in 49% of children at the 5year follow up visit, and responses were predicted to be undetectable in 69% (95% CI 45–88%) of children by the time of their teenage booster at 13–14years of age. There is no defined correlate of protection for pertussis. However, the large proportion of participants in this study with undetectable pertussis antibody levels at both measured and predicted timepoints suggests sub-optimal immunity in adolescence. Adding pertussis to the teenage booster for UK children as is done in other countries, would enhance immunity in adolescence.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>27364096</pmid><doi>10.1016/j.vaccine.2016.06.051</doi><tpages>8</tpages></addata></record>
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subjects Adolescent
Adolescents
Age
Antibodies, Bacterial - blood
Antibodies, Viral - blood
Antibody Formation
Antigens
Child
Child, Preschool
Children
Confidence intervals
Diphtheria
Diphtheria-Tetanus-acellular Pertussis Vaccines - administration & dosage
Diphtheria-Tetanus-acellular Pertussis Vaccines - therapeutic use
Diphtheria-Tetanus-Pertussis Vaccine - administration & dosage
Diphtheria-Tetanus-Pertussis Vaccine - therapeutic use
Female
Follow-Up Studies
Humans
Immunization, Secondary
Immunogenicity
Immunoglobulins
Infections
Kinetics
Laboratories
Male
Methods
Persistence
Pertussis
Polio
Poliomyelitis
Poliovirus Vaccine, Inactivated - administration & dosage
Poliovirus Vaccine, Inactivated - therapeutic use
Poliovirus Vaccine, Oral - administration & dosage
Poliovirus Vaccine, Oral - therapeutic use
Public health
Tetanus
Toxoids - immunology
United Kingdom
Vaccines
Vaccines, Combined - administration & dosage
Vaccines, Combined - therapeutic use
Whooping cough
title The predicted persistence and kinetics of antibody decline 9years after pre-school booster vaccination in UK children
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