The meningitis vaccine project

被引:112
作者
LaForce, F. Marc
Konde, Kader
Viviani, Simonetta
Preziosi, Marie-Pierre
机构
[1] PATH, Meningitis Vaccine Project, F-01210 Ferney Voltaire, France
[2] WHO, Meningitis Vaccine Project, Ferney Voltaire, France
关键词
meningococcal meningitis; meningococcal conjugate vaccine; public-private partnerships;
D O I
10.1016/j.vaccine.2007.04.049
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Epidemic meningococcal meningitis is an important public health problem in sub-Saharan Africa. Current control measures rely on reactive immunizations with polysaccharide (PS) vaccines that do not induce herd immunity and are of limited effectiveness in those under 2 years of age. Conversely, polysaccharide conjugate vaccines are effective in infants and have consistently shown an important effect on decreasing carriage. two characteristics that facilitate disease control. In 2001 the Meningitis Vaccine Project (MVP) was created as a partnership between PATH and the World Health Organization (WHO) with the goal of eliminating meningococcal epidemics in Africa through the development, licensure. introduction, and widespread use of conjugate meningococcal vaccines. Since group A Neisseria meningitidis (N. meningitidis) is the dominant pathogen causing epidemic meningitis in Africa MVP is developing an affordable (US$ 0.40 per dose) meningococcal A (Men A) conjugate vaccine through an innovative international partnership that saw transfer of a conjugation and fermentation technology to a developing country vaccine manufacturer. A Phase I study of the vaccine in India has shown that the product is safe and immunogenic. Phase 2 studies have begun in Africa, and a large demonstration study of the conjugate vaccine is envisioned for 2008-2009. After extensive consultations with African public health officials a vaccine introduction plan has been developed that includes introduction of the Men A conjugate vaccine into standard Expanded Programme on Immunization (EPI) schedules but also emphasizes mass vaccination of 1-29 years old to induce herd immunity, a strategy that has been shown to be highly effective when the meningococcal C (Men Q conjugate vaccine was introduced in several European countries. The MVP model is a clear example of the usefulness of a "push mechanism" to finance the development of a needed vaccine for the developing world. (C) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:A97 / A100
页数:4
相关论文
共 17 条
[1]   Meningococcal meningitis in Africa [J].
Greenwood, B .
TRANSACTIONS OF THE ROYAL SOCIETY OF TROPICAL MEDICINE AND HYGIENE, 1999, 93 (04) :341-353
[2]   MENINGOCOCCAL CARRIAGE, MENINGOCOCCAL DISEASE AND VACCINATION [J].
HASSANKING, MKA ;
WALL, RA ;
GREENWOOD, BM .
JOURNAL OF INFECTION, 1988, 16 (01) :55-&
[3]   Meningococcal conjugate vaccine for Africa:: a model for development of new vaccines for the poorest countries [J].
Jódar, L ;
LaForce, FM ;
Ceccarini, C ;
Aguado, T ;
Granoff, DM .
LANCET, 2003, 361 (9372) :1902-1904
[4]  
KSHIRSAGAR N, 2007, VACCINE
[5]  
Lapeyssonnie L., 1963, B WHO S, V28, P3
[6]   Carriage of serogroup C meningococci 1 year after meningococcal C conjugate polysaccharide vaccination [J].
Maiden, MCJ ;
Stuart, JM .
LANCET, 2002, 359 (9320) :1829-1830
[7]   Planning, registration, and implementation of an immunisation campaign against meningococcal serogroup C disease in the UK: a success story [J].
Miller, E ;
Salisbury, D ;
Ramsay, M .
VACCINE, 2001, 20 :S58-S67
[8]   Herd immunity from meningococcal serogroup C conjugate vaccination in England: database analysis [J].
Ramsay, ME ;
Andrews, NJ ;
Trotter, CL ;
Kaczmarski, EB ;
Miller, E .
BRITISH MEDICAL JOURNAL, 2003, 326 (7385) :365-366
[9]  
REINGOLD AL, 1985, LANCET, V2, P114
[10]   PREPARATION, CHARACTERIZATION, AND IMMUNOGENICITY OF HEMOPHILUS-INFLUENZAE TYPE-B POLYSACCHARIDE-PROTEIN CONJUGATES [J].
SCHNEERSON, R ;
BARRERA, O ;
SUTTON, A ;
ROBBINS, JB .
JOURNAL OF EXPERIMENTAL MEDICINE, 1980, 152 (02) :361-376