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Infection and Immunity, September 2002, p. 4946-4954, Vol. 70, No. 9
0019-9567/02/$04.00+0 DOI: 10.1128/IAI.70.9.4946-4954.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.
Effect of Vaccination with Carrier Protein on Response to Meningococcal C Conjugate Vaccines and Value of Different Immunoassays as Predictors of Protection
Moya Burrage,1 Andrew Robinson,1 Ray Borrow,2 Nick Andrews,3 Joanna Southern,3 Jamie Findlow,2 Sarah Martin,2 Carol Thornton,1 David Goldblatt,4 Michael Corbel,5 Dorothea Sesardic,5 Keith Cartwight,6 Peter Richmond,3 and Elizabeth Miller3*
Centre for Applied Microbiology and Research, Porton Down, Salisbury, Wiltshire,1
PHLS Meningococcal Reference Unit, Withington Hospital, Manchester,2
Immunisation Division, Communicable Disease Surveillance Centre, Public Health Laboratory Service,3
Immunobiology Unit, Institute of Child Health, London,4
National Institute for Biological Standards and Control, South Mimms, Potters Bar, Hertfordshire,5
Gloucester Vaccine Evaluation Unit, Public Health Laboratory, Gloucestershire Royal Hospital, Gloucester, United Kingdom6
Received 26 December 2001/
Returned for modification 15 March 2002/
Accepted 29 May 2002
In order to plan for the wide-scale introduction of meningococcal C conjugate (MCC) vaccine for United Kingdom children up to 18 years old, phase II trials were undertaken to investigate whether there was any interaction between MCC vaccines conjugated to tetanus toxoid (TT) or a derivative of diphtheria toxin (CRM197) and diphtheria-tetanus vaccines given for boosting at school entry or leaving. Children (n = 1,766) received a diphtheria-tetanus booster either 1 month before, 1 month after, or concurrently with one of three MCC vaccines conjugated to CRM197 or TT. All of the MCC vaccines induced high antibody responses to the serogroup C polysaccharide that were indicative of protection. The immune response to the MCC-TT vaccine was reduced as a result of prior immunization with a tetanus-containing vaccine, but antibody levels were still well above the lower threshold for protection. Prior or simultaneous administration of a diphtheria-containing vaccine did not affect the response to MCC-CRM197 vaccines. The immune responses to the carrier proteins were similar to those induced by a comparable dose of diphtheria or tetanus vaccine. The results also demonstrate that, for these conjugate vaccines in these age groups, both standard enzyme-linked immunosorbent assays and those that measure high-avidity antibodies to meningococcal C polysaccharide correlated equally well with assays that measure serum bactericidal antibodies, the established serological correlate of protection for MCC vaccines.
* Corresponding author. Mailing address: Immunisation Division, Communicable Disease Surveillance Centre, Public Health Laboratory Service, 61 Colindale Ave., London NW9 5EQ, United Kingdom. Phone: 44 0 181 200 6868. Fax: 44 0 181 200 7868. E-mail:
Emiller{at}phls.org.uk.
Editor: J. D. Clements
Infection and Immunity, September 2002, p. 4946-4954, Vol. 70, No. 9
0019-9567/02/$04.00+0 DOI: 10.1128/IAI.70.9.4946-4954.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.
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