Division of Infection, Inflammation and Immunity, University of Southampton School of Medicine, UK.
Southampton NIHR Respiratory Biomedical Research Unit, Division of Infection, Inflammation and Immunity, Southampton University School of Medicine, UK.
J Med Microbiol. 2011 Jan;60(Pt 1):1-8. doi: 10.1099/jmm.0.020016-0. Epub 2010 Oct 21.
Streptococcus pneumoniae, also known as the pneumococcus, is an important cause of morbidity and mortality in the developed and developing world. Pneumococcal conjugate vaccines were first introduced for routine use in the USA in 2000, although the seven-valent pneumococcal conjugate vaccine (PCV7) was not introduced into the UK's routine childhood immunization programme until September 2006. After its introduction, a marked decrease in the incidence of pneumococcal disease was observed, both in the vaccinated and unvaccinated UK populations. However, pneumococci are highly diverse and serotype prevalence is dynamic. Conversely, PCV7 targets only a limited number of capsular types, which appears to confer a limited lifespan to the observed beneficial effects. Shifts in serotype distribution have been detected for both non-invasive and invasive disease reported since PCV7 introduction, both in the UK and elsewhere. The pneumococcal Haemophilus influenzae protein D conjugate vaccine (PHiD-CV, Synflorix; GlaxoSmithKline) and 13-valent pneumococcal conjugate vaccine (PCV13, Prevenar 13; Pfizer) have been newly licensed. The potential coverage of the 10- and 13-valent conjugate vaccines has also altered alongside serotype shifts. Nonetheless, the mechanism of how PCV7 has influenced serotype shift is not clear-cut as the epidemiology of serotype prevalence is complex. Other factors also influence prevalence and incidence of pneumococcal carriage and disease, such as pneumococcal diversity, levels of antibiotic use and the presence of risk groups. Continued surveillance and identification of factors influencing serotype distribution are essential to allow rational vaccine design, implementation and continued effective control of pneumococcal disease.
肺炎链球菌,也称为肺炎球菌,是发达国家和发展中国家发病率和死亡率的重要原因。肺炎球菌结合疫苗于 2000 年首次在美国常规使用,尽管 7 价肺炎球菌结合疫苗(PCV7)直到 2006 年 9 月才引入英国常规儿童免疫计划。引入后,在接种和未接种疫苗的英国人群中,观察到肺炎球菌病的发病率明显下降。然而,肺炎球菌高度多样化,血清型流行情况是动态的。相反,PCV7 仅针对有限数量的荚膜型,这似乎赋予了观察到的有益效果有限的寿命。自 PCV7 引入以来,无论是在英国还是其他地方,都检测到了非侵袭性和侵袭性疾病报告中血清型分布的变化。肺炎球菌流感嗜血杆菌蛋白 D 结合疫苗(PHiD-CV,Synflorix;葛兰素史克)和 13 价肺炎球菌结合疫苗(PCV13,Prevnar 13;辉瑞)已获得新的许可。10 价和 13 价结合疫苗的潜在覆盖率也随着血清型转变而改变。尽管如此,PCV7 如何影响血清型转变的机制并不明确,因为血清型流行的流行病学是复杂的。其他因素也会影响肺炎球菌携带和疾病的流行率和发病率,例如肺炎球菌的多样性、抗生素使用水平以及存在风险群体。持续监测和确定影响血清型分布的因素对于合理的疫苗设计、实施以及持续有效地控制肺炎球菌病至关重要。