Meningococcal group C conjugate vaccines
Open Access
- 1 May 2001
- journal article
- research article
- Published by BMJ in Archives of Disease in Childhood
- Vol. 84 (5), 383-386
- https://doi.org/10.1136/adc.84.5.383
Abstract
Every paediatrician knows the severity of invasive meningococcal disease and the speed at which previously healthy children can become prostrate. Five major serogroups (A, B, C, Y, and W135) are responsible for the majority of disease, the serogroup being determined by the nature of the capsular polysaccharide. The prevalence of different serogroups varies in different regions and in different age groups. Globally the greatest burden of disease comes from serogroup A which is responsible for massive epidemics in the “meningitis belt” of sub-Saharan Africa and an endemic rate which is more than 10 times that in industrialised countries.2 In much of Western Europe including the UK, more than 90% of disease is caused by serogroups B and C. Serogroup C accounts for 25–40% of cases, with the relative proportion varying in a cyclical manner from year to year. In 1995, there were 1890 reported cases of invasive meningococcal disease, an increase of 43% on the previous year.3 The majority of the increase was caused by serogroup C. Numbers of reported cases continued to rise in subsequent years, reaching a 50 year high in 1997 of 2659.4 The rise in numbers may be partly a result of better case ascertainment, but it has also coincided with the emergence of a new serogroup C clone named “ET-37” which has been responsible for a number of outbreaks of disease in many countries around the world.5-12 Many of these have attracted intense media attention. By far the majority of people with invasive disease are healthy individuals under the age of 20 with no apparent risk factors for disease. The peak incidence of disease is in infants under 1 year of age with a second peak in older teenagers.13 While 40% of disease is caused by group C in all age groups, there are more deaths attributed to serogroup C than serogroup B in the 11–24 year age group.14Keywords
This publication has 40 references indexed in Scilit:
- Mucosal Immune Responses to Meningococcal Group C Conjugate and Group A and C Polysaccharide Vaccines in AdolescentsInfection and Immunity, 2000
- Meningococcal serogroup C-specific IgG antibody responses and serum bactericidal titres in children following vaccination with a meningococcal A/C polysaccharide vaccineFEMS Immunology & Medical Microbiology, 2000
- Induction of Immunologic Memory in Gambian Children by Vaccination in Infancy with a Group A plus Group C Meningococcal Polysaccharide-Protein Conjugate VaccineThe Journal of Infectious Diseases, 1997
- Conjugate Meningococcal Serogroup A and C Vaccine: Reactogenicity and Immunogenicity in United Kingdom InfantsThe Journal of Infectious Diseases, 1996
- Total and functional antibody response to a quadrivalent meningococcal polysaccharide vaccine among childrenThe Journal of Pediatrics, 1996
- A Trial Of A Group A Plus Group C Meningococcal Polysaccharide-ProteinThe Journal of Infectious Diseases, 1995
- Pneumococcal disease: prospects for a new generation of vaccinesScience, 1994
- Antigenic and Epidemiologic Properties of the ET-37 Complex of Neisseria meningitidisThe Journal of Infectious Diseases, 1993
- Escherichia coli K51 and K93 capsular polysaccharides are crossreactive with the group A capsular polysaccharide of Neisseria meningitidis. Immunochemical, biological, and epidemiological studies.The Journal of Experimental Medicine, 1985
- AGE-SPECIFIC DIFFERENCES IN DURATION OF CLINICAL PROTECTION AFTER VACCINATION WITH MENINGOCOCCAL POLYSACCHARIDE A VACCINEThe Lancet, 1985