LaForce F Marc, Konde Kader, Viviani Simonetta, Préziosi Marie-Pierre
The Meningitis Vaccine Project, PATH, 13 Chemin du Levant, 01210 Ferney-Voltaire, France.
Vaccine. 2007 Sep 3;25 Suppl 1:A97-100. doi: 10.1016/j.vaccine.2007.04.049. Epub 2007 May 7.
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 1 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 C) 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.
流行性脑膜炎球菌性脑膜炎是撒哈拉以南非洲地区一个重要的公共卫生问题。目前的控制措施依赖于使用多糖(PS)疫苗进行应急免疫接种,这种疫苗不会诱导群体免疫,且对2岁以下儿童的有效性有限。相反,多糖结合疫苗对婴儿有效,并且一直显示出对减少带菌状态有重要作用,这两个特性有助于疾病控制。2001年,脑膜炎疫苗项目(MVP)作为PATH与世界卫生组织(WHO)的合作项目成立,目标是通过开发、许可、引进和广泛使用结合型脑膜炎球菌疫苗来消除非洲的脑膜炎球菌流行疫情。由于A群脑膜炎奈瑟菌(N. meningitidis)是在非洲引起流行性脑膜炎的主要病原体,MVP正在通过一项创新的国际合作项目开发一种价格亲民(每剂0.4美元)的A群脑膜炎球菌(Men A)结合疫苗,该项目涉及将结合和发酵技术转让给一家发展中国家的疫苗生产商。该疫苗在印度进行的1期研究表明,该产品安全且具有免疫原性。2期研究已在非洲启动,预计2008 - 2009年将开展一项关于该结合疫苗的大型示范研究。在与非洲公共卫生官员进行广泛磋商后,制定了一项疫苗引进计划,该计划不仅包括将Men A结合疫苗纳入标准的扩大免疫规划(EPI)日程,还强调对1至29岁人群进行大规模接种以诱导群体免疫,当脑膜炎球菌C(Men C)结合疫苗在几个欧洲国家引进时,这一策略已被证明非常有效。MVP模式是一个“推动机制”有助于为发展中世界开发所需疫苗提供资金的明显例证。