Aguado M Teresa, Jodar Luis, Granoff Dan, Rabinovich Regina, Ceccarini Costante, Perkin Gordon W
Vaccines and Immunization Consultant, Versoix, Switzerland.
Pfizer Inc, New York City, New York.
Clin Infect Dis. 2015 Nov 15;61 Suppl 5(Suppl 5):S391-5. doi: 10.1093/cid/civ593.
Polysaccharide vaccines had been used to control African meningitis epidemics for >30 years but with little or modest success, largely because of logistical problems in the implementation of reactive vaccination campaigns that are begun after epidemics are under way. After the major group A meningococcal meningitis epidemics in 1996-1997 (250,000 cases and 25,000 deaths), African ministers of health declared the prevention of meningitis a high priority and asked the World Health Organization (WHO) for help in developing better immunization strategies to eliminate meningitis epidemics in Africa.
WHO accepted the challenge and created a project called Epidemic Meningitis Vaccines for Africa (EVA) that served as an organizational framework for external consultants, PATH, the US Centers for Disease Control and Prevention (CDC), and the Bill & Melinda Gates Foundation (BMGF). Consultations were initiated with major vaccine manufacturers. EVA commissioned a costing study/business plan for the development of new group A or A/C conjugate vaccines and explored the feasibility of developing these products as a public-private partnership. Representatives from African countries were consulted. They confirmed that the development of conjugate vaccines was a priority and provided information on preferred product characteristics. In parallel, a strategy for successful introduction was also anticipated and discussed.
The expert consultations recommended that a group A meningococcal conjugate vaccine be developed and introduced into the African meningitis belt. The results of the costing study indicated that the "cost of goods" to develop a group A - containing conjugate vaccine in the United States would be in the range of US$0.35-$1.35 per dose, depending on composition (A vs A/C), number of doses/vials, and presentation. Following an invitation from BMGF, a proposal was submitted in the spring of 2001.
In June 2001, BMGF awarded a grant of US$70 million to create the Meningitis Vaccine Project (MVP) as a partnership between PATH and WHO, with the specific goal of developing an affordable MenA conjugate vaccine to eliminate MenA meningitis epidemics in Africa. EVA is an example of the use of WHO as an important convening instrument to facilitate new approaches to address major public health problems.
多糖疫苗已被用于控制非洲脑膜炎流行30多年,但成效甚微或仅有一定成效,主要是因为在疫情爆发后开展的应急疫苗接种活动在实施过程中存在后勤问题。在1996 - 1997年发生主要的A群脑膜炎球菌性脑膜炎疫情(25万例病例和2.5万例死亡)后,非洲各国卫生部长宣布预防脑膜炎为高度优先事项,并请求世界卫生组织(WHO)协助制定更好的免疫策略,以消除非洲的脑膜炎疫情。
WHO接受了这一挑战,创建了一个名为“非洲流行性脑膜炎疫苗”(EVA)的项目,该项目为外部顾问、PATH、美国疾病控制与预防中心(CDC)以及比尔及梅琳达·盖茨基金会(BMGF)提供了一个组织框架。与主要疫苗制造商展开了磋商。EVA委托进行了一项关于开发新的A群或A/C群结合疫苗的成本核算研究/商业计划,并探讨了通过公私合营开发这些产品的可行性。咨询了非洲国家的代表。他们确认结合疫苗的开发是一个优先事项,并提供了关于首选产品特性的信息。与此同时,还预期并讨论了成功引入疫苗的策略。
专家磋商建议开发一种A群脑膜炎球菌结合疫苗并引入非洲脑膜炎带。成本核算研究结果表明,在美国开发一种含A群的结合疫苗的“商品成本”每剂在0.35 - 1.35美元之间,具体取决于成分(A群与A/C群)、剂量/瓶数以及剂型。应BMGF邀请,于2001年春季提交了一份提案。
2001年6月,BMGF授予7000万美元赠款,创建了脑膜炎疫苗项目(MVP),作为PATH与WHO之间的合作伙伴关系,其具体目标是开发一种价格可承受的A群脑膜炎球菌结合疫苗,以消除非洲的A群脑膜炎球菌性脑膜炎疫情。EVA是利用WHO作为重要召集工具来推动解决重大公共卫生问题新方法的一个范例。