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M D Snape, senior clinical research fellow1, D F Kelly, clinical lecturer1, S Lewis, research assistant1, C Banner, research assistant1, L Kibwana, research assistant1, C E Moore, post-doctoral research assistant1, L Diggle, principal research nurse1, T John, senior research nurse1, L M Yu, statistician2, R Borrow, consultant clinical scientist3, A Borkowski, clinical trials director4, C Nau, clinical research assistant4, A J Pollard, reader in paediatric infection and immunity1
1 Oxford Vaccine Group, Department of Paediatrics, University of Oxford, Centre for Clinical Vaccinology and Tropical Medicine, Churchill Hospital, Oxford OX3 7LJ, 2 Centre for Statistics in Medicine, University of Oxford, 3 Vaccine Evaluation Unit, Health Protection Agency, Manchester, 4 Novartis Vaccines, Marburg, Germany
Correspondence to: M Snape matthew.snape{at}paediatrics.ox.ac.uk
Design Observational study.
Setting Secondary and tertiary educational institutions in the United Kingdom.
Participants Healthy adolescents aged 11-20 years previously immunised between 6 and 15 years of age with one of the three serogroup C meningococcal vaccines.
Intervention Serum obtained by venepuncture.
Main outcome measures Percentage of participants with (rabbit complement) serum bactericidal antibody titres of at least 1:8; geometric mean titres of serogroup C meningococcal serum bactericidal antibody.
Results Five years after immunisation, 84.1% (95% confidence interval 81.6% to 86.3%) of 987 participants had a bactericidal antibody titre of at least 1:8. Geometric mean titres of bactericidal antibody were significantly lower in 11-13 year olds (147, 95% confidence interval 115 to 188) than in 14-16 year olds (300, 237 to 380) and 17-20 year olds (360, 252 to 515) (P<0.0001 for both comparisons). Within these age bands, no significant difference in geometric mean titres of bactericidal antibody between recipients of the different serogroup C meningococcal vaccines was seen. More than 70% of participants had received a vaccine from one manufacturer; in this cohort, geometric mean titres were higher in those immunised at aged 10 years or above than in those immunised before the age of 10.
Conclusions Higher concentrations of bactericidal antibody are seen five years after immunisation with serogroup C meningococcal vaccine at age 10 years or above than in younger age groups, possibly owing to immunological maturation. This provides support for adolescent immunisation programmes to generate sustained protection against serogroup C meningococcal disease not only for the vaccine recipients but also, through the maintenance of herd immunity, for younger children.
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