National Reference Centre for Streptococcus pneumoniae, University Hospitals Leuven, Leuven, Belgium; Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium.
National Reference Centre for Streptococcus pneumoniae, University Hospitals Leuven, Leuven, Belgium; Department of Microbiology, Immunology and Transplantation, KU Leuven, Leuven, Belgium.
Lancet Infect Dis. 2021 Jan;21(1):127-136. doi: 10.1016/S1473-3099(20)30173-0. Epub 2020 Jul 20.
Ten-valent and 13-valent pneumococcal conjugate vaccines (PCVs) have shown important benefits by decreasing invasive pneumococcal disease caused by vaccine serotypes. Belgium had an uncommon situation with sequential use of PCV7, PCV13, and PCV10 in the childhood vaccination programmes between 2007 and 2018. We aimed to analyse the changes in incidence of invasive pneumococcal disease and serotype distribution in children throughout this period.
Streptococcus pneumoniae isolates were obtained from patients with invasive pneumococcal disease in Belgium between 2007 and 2018 by the national laboratory-based surveillance. Paediatric invasive pneumococcal disease incidence, serotype distribution, and antimicrobial susceptibility were analysed in periods during which PCV7 (2009-10), PCV13 (2013-14), both PCV13 and PCV10 (2015-16), and PCV10 (2017-18) were used. Incidence rates and trends were compared. Vaccination status was collected. For a subset of serotype 19A isolates, multilocus sequence type was identified.
After a decrease in PCV7 serotype invasive pneumococcal disease was observed during the PCV7 period, total paediatric invasive pneumococcal disease incidence significantly declined during the PCV13 period (-2·6% monthly, p<0·0001). During the PCV13-PCV10 period (2015-16), the lowest mean in paediatric invasive pneumococcal disease incidence was achieved, but the incidence increased again during the PCV10 period (2017-18), especially in children younger than 2 years (+1·7% monthly; p=0·028). This increase was mainly due to a significant rise in serotype 19A invasive pneumococcal disease incidence in the PCV10 period compared with the PCV13 period (p<0·0001), making serotype 19A the predominant serotype in paediatric invasive pneumococcal disease in the PCV10 period. Genetic diversity within the 2017-18 serotype 19A collection was seen, with two predominant clones, ST416 and ST994, that were infrequently observed before PCV10 introduction. In 2018, among children younger than 5 years with invasive pneumococcal disease who were correctly vaccinated, 37% (37 of 100) had PCV13 serotype invasive pneumococcal disease, all caused by serotype 19A and serotype 3.
After a significant decrease during the PCV13 period, paediatric invasive pneumococcal disease incidence increased again during the PCV10 period. This observation mainly resulted from a significant increase of serotype 19A cases. During the PCV10 period, dominant serotype 19A clones differed from those detected during previous vaccine periods. Whether changes in epidemiology resulted from the vaccine switch or also from natural evolution remains to be further elucidated.
The Belgian National Reference is funded by the Belgian National Institute for Health and Disability Insurance and the whole genome sequencing by an investigator-initiated research grant from Pfizer.
十价和十三价肺炎球菌结合疫苗(PCV)通过降低疫苗血清型引起的侵袭性肺炎球菌病,显示出重要的益处。比利时在 2007 年至 2018 年期间,儿童免疫规划中先后使用了 PCV7、PCV13 和 PCV10,情况较为特殊。本研究旨在分析在此期间儿童侵袭性肺炎球菌病的发病率和血清型分布变化。
通过国家实验室监测,获取 2007 年至 2018 年期间比利时侵袭性肺炎球菌病患者的肺炎链球菌分离株。分析了 PCV7 时期(2009-10 年)、PCV13 时期(2013-14 年)、PCV13 和 PCV10 联合使用时期(2015-16 年)以及 PCV10 时期(2017-18 年)的儿童侵袭性肺炎球菌病发病率、血清型分布和抗菌药物敏感性。比较发病率和趋势。收集疫苗接种情况。对部分 19A 血清型分离株进行多位点序列分型。
在 PCV7 时期侵袭性肺炎球菌病的 PCV7 血清型发病率下降后,PCV13 时期儿童侵袭性肺炎球菌病总发病率显著下降(每月下降 2.6%,p<0.0001)。在 PCV13-PCV10 时期(2015-16 年),儿童侵袭性肺炎球菌病发病率达到最低,但在 PCV10 时期(2017-18 年)发病率再次上升,尤其是在 2 岁以下儿童中(每月增加 1.7%;p=0.028)。这种上升主要是由于 PCV10 时期 19A 血清型侵袭性肺炎球菌病发病率与 PCV13 时期相比显著上升(p<0.0001)所致,使 19A 血清型成为 PCV10 时期儿童侵袭性肺炎球菌病的主要血清型。在 2017-18 年的 19A 血清型分离株中观察到遗传多样性,有两个主要克隆,ST416 和 ST994,这在 PCV10 引入之前很少观察到。在 2018 年,5 岁以下正确接种疫苗的侵袭性肺炎球菌病患儿中,37%(100 例中的 37 例)为 PCV13 血清型侵袭性肺炎球菌病,均由血清型 19A 和血清型 3 引起。
在 PCV13 时期显著下降后,PCV10 时期儿童侵袭性肺炎球菌病发病率再次上升。这一观察结果主要是由于 19A 血清型病例显著增加所致。在 PCV10 时期,主要的 19A 克隆与之前疫苗时期检测到的不同。流行病学的变化是由于疫苗转换还是自然进化引起的,仍有待进一步阐明。
这段译文是基于文本内容直接翻译的,可能存在一些不符合中文表达习惯的地方。