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从公共卫生政策角度看脑膜炎球菌病。

Meningococcal disease from the public health policy perspective.

机构信息

Center for Global Health, Cincinnati Children's Hospital, 3333 Burnet Avenue, Cincinnati, OH 45229, USA.

出版信息

Vaccine. 2012 May 30;30 Suppl 2:B37-9. doi: 10.1016/j.vaccine.2011.12.074.

Abstract

The incidence and serogroup distribution of meningococcal disease vary by country and over time. In the United States, the annual incidence has been 0.5-1.1/100,000 or about 1400-2800 cases annually with the highest incidence being in infants less than six months of age [1]. Given the availability of conjugate vaccines against serogroups A, C, W-135 and Y and the possible future availability of a group B vaccine, there is now the potential to effectively control meningococcal disease globally. The question then arises as to how public health policy can best serve this goal. MCV-D (Menactra) is not immunogenic in the first six months of life. For this reason, it has been proposed that immunization with this vaccine begin at nine months of age with a second dose at 12 months. This proposal would rely upon indirect or "herd protection" to protect young infants with the highest disease incidence. A second vaccine, MCV-CRM (Menveo), is immunogenic in the first months of life and is under consideration by the FDA for use in infants two months of age and older. MCV-CRM could provide direct protection of this high risk group, but three primary doses plus a toddler booster are required for this approach. In developing public health recommendations to protect infants, policy makers must weigh the additional cost of immunizing with four doses versus the possibility that relying on herd protection using a lower cost immunization schedule beginning at nine months of age may leave young infants unprotected. Optimal control of meningococcal disease will require both the public will and public policy to best serve this goal. The decision as to what ages to target and which schedules to use should not only take into account the cost of the program, but also the severity of the disease and the high level public concern regarding meningococcal disease.

摘要

脑膜炎球菌病的发病率和血清型分布因国家和时间而异。在美国,年发病率为 0.5-1.1/10 万,每年约有 1400-2800 例,发病率最高的是不到 6 个月大的婴儿[1]。鉴于有针对血清型 A、C、W-135 和 Y 的结合疫苗,以及可能未来有针对血清型 B 的疫苗,现在有可能在全球有效控制脑膜炎球菌病。那么,公共卫生政策如何才能最好地实现这一目标呢?MCV-D(Menactra)在生命的前 6 个月内没有免疫原性。因此,有人提议从 9 个月大开始接种这种疫苗,12 个月时再接种第二剂。这一建议将依靠间接或“群体保护”来保护发病率最高的婴幼儿。第二种疫苗 MCV-CRM(Menveo)在生命的头几个月具有免疫原性,正在接受 FDA 考虑用于 2 个月及以上的婴儿。MCV-CRM 可以为这一高风险群体提供直接保护,但这种方法需要接种三剂基础疫苗加一剂幼儿加强针。在制定保护婴儿的公共卫生建议时,决策者必须权衡用四剂疫苗进行免疫的额外成本,以及依靠从 9 个月大开始使用成本较低的免疫计划来实现群体保护的可能性,这种可能性可能会使婴幼儿得不到保护。最佳控制脑膜炎球菌病需要公众意愿和公共政策共同来实现这一目标。针对哪些年龄组进行免疫接种以及使用哪种免疫接种时间表的决策,不仅应考虑到方案的成本,还应考虑到疾病的严重程度以及公众对脑膜炎球菌病的高度关注。

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