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1998 - 2005年,八个州引入结合疫苗5年后儿童侵袭性肺炎球菌疾病情况

Invasive pneumococcal disease in children 5 years after conjugate vaccine introduction--eight states, 1998-2005.

出版信息

MMWR Morb Mortal Wkly Rep. 2008 Feb 15;57(6):144-8.

PMID:18272956
Abstract

Streptococcus pneumoniae (pneumococcus) is a major cause of meningitis, pneumonia, and bacteremia, especially among young children and older adults. Before the 7-valent pneumococcal conjugate vaccine (PCV7) was introduced in the United States in 2000, the seven pneumococcal serotypes covered by the vaccine (4, 6B, 9V, 14, 18C, 19F, and 23F) caused 80% of invasive pneumococcal disease (IPD) cases among young children, and the incidence of IPD was relatively stable. In October 2000, the Advisory Committee on Immunization Practices recommended PCV7 for all children aged <2 years and for older children at increased risk for IPD. Introduction of PCV7 in the United States led to substantial reductions in the incidence of IPD among the target population of children aged <5 years. Use of the vaccine also reduced IPD among unvaccinated populations through reductions in nasopharyngeal colonization and transmission of vaccine-type pneumococci from vaccinated children (i.e., indirect, or herd, effects of PCV7). To evaluate the effect of continued PCV7 use on IPD incidence among children aged <5 years in the United States, CDC analyzed population- and laboratory-based surveillance data. Results of that analysis indicated that in 2005, overall IPD rates among children aged <5 years were 77% lower, and an estimated 13,000 fewer cases of IPD occurred, compared with the years preceding vaccine introduction (1998-1999). Although IPD caused by PCV7 serotypes declined through 2005, overall IPD rates leveled off beginning in 2002, primarily because of increases in the incidence of IPD caused by non-PCV7 serotype 19A. Given these trends, use of expanded-valency conjugate vaccines might further reduce IPD incidence. Continued surveillance is needed to guide development of future formulations of conjugate vaccines and to monitor the effects of continued vaccine use.

摘要

肺炎链球菌是脑膜炎、肺炎和菌血症的主要病因,在幼儿和老年人中尤为常见。2000年美国引入7价肺炎球菌结合疫苗(PCV7)之前,该疫苗涵盖的7种肺炎球菌血清型(4、6B、9V、14、18C、19F和23F)导致幼儿侵袭性肺炎球菌病(IPD)病例的80%,且IPD发病率相对稳定。2000年10月,免疫实践咨询委员会建议对所有2岁以下儿童以及患IPD风险增加的大龄儿童接种PCV7。在美国引入PCV7后,5岁以下目标儿童群体中IPD发病率大幅降低。使用该疫苗还通过减少鼻咽部定植以及接种疫苗儿童中疫苗型肺炎球菌的传播,降低了未接种疫苗人群中的IPD发病率(即PCV7的间接或群体效应)。为评估在美国持续使用PCV7对5岁以下儿童IPD发病率的影响,美国疾病控制与预防中心分析了基于人群和实验室的监测数据。该分析结果表明,与疫苗引入前的年份(1998 - 1999年)相比,2005年5岁以下儿童的总体IPD发病率降低了77%,估计IPD病例减少了13,000例。尽管由PCV7血清型引起的IPD在2005年之前有所下降,但总体IPD发病率自2002年起趋于平稳,主要原因是非PCV7血清型19A引起的IPD发病率增加。鉴于这些趋势,使用更高价的结合疫苗可能会进一步降低IPD发病率。需要持续监测以指导未来结合疫苗配方的研发,并监测疫苗持续使用的效果。

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