Vestjens Stefan M T, Wagenvoort Gertjan H J, Grutters Jan C, Meek Bob, Aldenkamp Arnoud F, Vlaminckx Bart J M, Bos Willem Jan W, Rijkers Ger T, van de Garde Ewoudt M W
Department of Internal Medicine, St. Antonius Hospital, Nieuwegein, The Netherlands.
Department of Medical Microbiology and Immunology, St. Antonius Hospital, Nieuwegein, The Netherlands.
Vaccine. 2017 Jul 24;35(33):4112-4118. doi: 10.1016/j.vaccine.2017.06.049. Epub 2017 Jun 28.
In 2006 a 7-valent pneumococcal conjugate vaccine (PCV7) was introduced in the immunisation programme for infants in The Netherlands and replaced by PCV10 in 2011. Limited data exist about the impact of PCV on the aetiology of CAP as a whole. The aim of the present study is to describe the overall changes in microbial aetiology, pneumococcal burden (including non-bacteraemic pneumococcal pneumonia) and its serotypes in adult community-acquired pneumonia (CAP) after the introduction of these PCVs.
Hospitalised adult CAP patients who participated in three consecutive trials were studied (2004-2006 (n=201), 2007-2009 (n=304) and 2012-2016 (n=300) and considered as pre-PCV7, PCV7 and PCV10 period). Extensive conventional microbiological testing was applied for all patients. In addition, patients with a serotype-specific pneumococcal antibody response were diagnosed with pneumococcal CAP. Changes in proportions of causative pathogens and distributions of pneumococcal serotypes were calculated.
The proportion of pneumococcal CAP decreased from 37% (n=74/201) to 26% (n=77/300) comparing the pre-PCV7 period with the PCV10 period (p=0.01). For other pathogens, including Legionella spp., Mycoplasma pneumoniae, S. aureus, H. influenzae, and respiratory viruses, no sustained shifts were observed in their relative contribution to the aetiology of CAP. Within the pneumococcal CAP patients, we observed a decrease in PCV7 and an increase in non-PCV10 serotype disease. PCV10-extra type disease did not decrease significantly comparing the PCV10 period with the pre-PCV7 and PCV7 period, respectively. Notably, PCV7 type disease decreased both in bacteraemic and non-bacteraemic patients.
Our findings confirm that PCV introduction in infants impact the microbial aetiology of adult CAP and suggest herd effects in adults with CAP after introduction of PCVs in children.
2006年,荷兰在婴儿免疫规划中引入了7价肺炎球菌结合疫苗(PCV7),并于2011年被PCV10取代。关于PCV对总体社区获得性肺炎(CAP)病因的影响的数据有限。本研究的目的是描述在引入这些PCV后,成人社区获得性肺炎(CAP)的微生物病因、肺炎球菌负担(包括非菌血症性肺炎球菌肺炎)及其血清型的总体变化。
对参加连续三项试验的住院成人CAP患者进行研究(2004 - 2006年(n = 201)、2007 - 2009年(n = 304)和2012 - 2016年(n = 300),分别视为PCV7前、PCV7和PCV10时期)。对所有患者进行了广泛的常规微生物检测。此外,对具有血清型特异性肺炎球菌抗体反应的患者诊断为肺炎球菌CAP。计算了致病病原体比例和肺炎球菌血清型分布的变化。
将PCV7前时期与PCV10时期相比,肺炎球菌CAP的比例从37%(n = 74/201)降至26%(n = 77/300)(p = 0.01)。对于其他病原体,包括嗜肺军团菌、肺炎支原体、金黄色葡萄球菌、流感嗜血杆菌和呼吸道病毒,它们对CAP病因的相对贡献未观察到持续变化。在肺炎球菌CAP患者中,我们观察到PCV7疾病减少,非PCV10血清型疾病增加。将PCV10时期分别与PCV7前和PCV7时期相比,PCV10额外血清型疾病没有显著下降。值得注意的是,菌血症和非菌血症患者的PCV7血清型疾病均减少。
我们的研究结果证实,婴儿接种PCV会影响成人CAP的微生物病因,并提示在儿童接种PCV后,成人CAP存在群体效应。