Department of Pediatrics, University Denis Diderot, Paris, France.
BMC Infect Dis. 2012 Sep 7;12:207. doi: 10.1186/1471-2334-12-207.
The burden of invasive pneumococcal disease in young children decreased dramatically following introduction of the 7-valent pneumococcal conjugate vaccine (PCV7). The epidemiology of S. pneumoniae now reflects infections caused by serotypes not included in PCV7. Recently introduced higher valency pneumococcal vaccines target the residual burden of invasive and non-invasive infections, including those caused by serotypes not included in PCV7. This review is based on presentations made at the European Society of Pediatric Infectious Diseases in June 2011.
Surveillance data show increased circulation of the non-PCV7 vaccine serotypes 1, 3, 6A, 6C, 7 F and 19A in countries with routine vaccination. Preliminary evidence suggests that broadened serotype coverage offered by higher valency vaccines may be having an effect on invasive disease caused by some of those serotypes, including 19A, 7 F and 6C. Aetiology of community acquired pneumonia remains a difficult clinical diagnosis. However, recent reports indicate that pneumococcal vaccination has reduced hospitalisations of children for vaccine serotype pneumonia. Variations in serotype circulation and occurrence of complicated and non-complicated pneumonia caused by non-PCV7 serotypes highlight the potential of higher valency vaccines to decrease the remaining burden. PCVs reduce nasopharyngeal carriage and acute otitis media (AOM) caused by vaccine serotypes. Recent investigations of the interaction between S. pneumoniae and non-typeable H. influenzae suggest that considerable reduction in severe, complicated AOM infections may be achieved by prevention of early pneumococcal carriage and AOM infections. Extension of the vaccine serotype spectrum beyond PCV7 may provide additional benefit in preventing the evolution of AOM. The direct and indirect costs associated with pneumococcal disease are high, thus herd protection and infections caused by non-vaccine serotypes both have strong effects on the cost effectiveness of pneumococcal vaccination. Recent evaluations highlight the public health significance of indirect benefits, prevention of pneumonia and AOM and coverage of non-PCV7 serotypes by higher valency vaccines.
Routine vaccination has greatly reduced the burden of pneumococcal diseases in children. The pneumococcal serotypes present in the 7-valent vaccine have greatly diminished among disease isolates. The prevalence of some non-vaccine serotypes (e.g. 1, 7 F and 19A) has increased. Pneumococcal vaccines with broadened serotype coverage are likely to continue decreasing the burden of invasive disease, and community acquired pneumonia in children. Further reductions in pneumococcal carriage and increased prevention of early AOM infections may prevent the evolution of severe, complicated AOM. Evaluation of the public health benefits of pneumococcal conjugate vaccines should include consideration of non-invasive pneumococcal infections, indirect effects of vaccination and broadened serotype coverage.
在 7 价肺炎球菌结合疫苗(PCV7)问世后,儿童侵袭性肺炎球菌病的负担显著下降。目前肺炎链球菌的流行病学反映了疫苗未覆盖血清型引起的感染。最近推出的高价肺炎球菌疫苗针对侵袭性和非侵袭性感染的剩余负担,包括疫苗未覆盖血清型引起的感染。本综述基于 2011 年 6 月欧洲儿科传染病学会的演讲。
监测数据显示,在常规接种疫苗的国家,非 PCV7 疫苗血清型 1、3、6A、6C、7F 和 19A 的循环增加。初步证据表明,高价疫苗更广泛的血清型覆盖可能对某些血清型引起的侵袭性疾病产生影响,包括 19A、7F 和 6C。社区获得性肺炎的病因仍然是一个困难的临床诊断。然而,最近的报告表明,肺炎球菌疫苗接种减少了儿童因疫苗血清型肺炎住院的情况。非 PCV7 血清型引起的社区获得性肺炎和复杂性与非复杂性肺炎的血清型循环变化突出表明,高价疫苗有可能进一步降低剩余负担。PCV 可降低疫苗血清型引起的鼻咽携带和急性中耳炎(AOM)。最近对肺炎链球菌和不可分型流感嗜血杆菌相互作用的研究表明,通过预防早期肺炎链球菌携带和 AOM 感染,可大大减少严重、复杂的 AOM 感染。在 PCV7 之外扩展疫苗血清型谱可能会在预防 AOM 演变方面提供额外的益处。肺炎球菌病相关的直接和间接成本都很高,因此群体保护和非疫苗血清型引起的感染对肺炎球菌疫苗接种的成本效益都有很强的影响。最近的评估强调了间接效益、预防肺炎和 AOM 以及高价疫苗对非 PCV7 血清型的覆盖的公共卫生意义。
常规接种大大降低了儿童肺炎球菌病的负担。7 价疫苗中的肺炎球菌血清型在疾病分离株中的比例大大降低。一些非疫苗血清型(如 1、7F 和 19A)的流行率有所增加。具有更广泛血清型覆盖范围的肺炎球菌疫苗可能会继续降低侵袭性疾病和儿童社区获得性肺炎的负担。进一步减少肺炎球菌携带和增加预防早期 AOM 感染可能会阻止严重、复杂的 AOM 的演变。评估肺炎球菌结合疫苗的公共卫生效益时,应考虑非侵袭性肺炎球菌感染、疫苗接种的间接影响和广泛的血清型覆盖。