Canadian Center for Vaccinology (CCfV), IWK Health Centre, Nova Scotia Health Authority (NSHA), and Dalhousie University, Halifax, NS, Canada.
Canadian Center for Vaccinology (CCfV), IWK Health Centre, Nova Scotia Health Authority (NSHA), and Dalhousie University, Halifax, NS, Canada.
Vaccine. 2019 Aug 23;37(36):5466-5473. doi: 10.1016/j.vaccine.2019.05.003. Epub 2019 Jul 23.
The 13-valent pneumococcal conjugate vaccine (PCV13) was recently shown to be effective against PCV13-type invasive pneumococcal disease (IPD) and pneumococcal community acquired pneumonia (CAP) in healthy adults aged ≥65 years, prompting many countries to re-assess adult immunization. In Canada, the potential benefits of adult PCV13 immunization were unclear given anticipated herd immunity from PCV13 childhood immunization introduced since 2010. This study describes the serotype distribution and clinical outcomes of Canadian adults aged ≥16 years, who were hospitalized with CAP and IPD from 2010 to 2015.
Active surveillance for CAP and IPD was performed in adult hospitals across five Canadian provinces. IPD was identified when Streptococcus pneumoniae was isolated from sterile sites. Bacteremic and non-bacteremic CAP were identified using blood culture, and sputum culture or PCV13-specific urine antigen detection (UAD), respectively. Serotype was assigned using Quellung reaction, PCR, or UAD.
Of 6687 CAP cases where a test was performed, S. pneumoniae positivity decreased from 15.9% in 2011 to 8.8% in 2014, but increased to 12.9% in 2015. CAP attributed to PCV13 serotypes followed a similar trend, dropping from 8.3% in 2010 to 4.6% in 2014, but increasing to 6.3% in 2015. The decline was primarily attributed to serotypes 7F and 19A, and the proportional increase to serotype 3. Similar trends were noted for bacteremic and non-bacteremic CAP. Serious outcomes such as 30-day mortality, intensive care unit admission, and requirement for mechanical ventilation were prominent in CAP and IPD cases, but remained unchanged over the study years.
Herd immunity afforded primarily by serotypes 7F and 19A appears to be partly masked by a concomitant proportional increase of serotype 3. Despite evidence of herd immunity, these PCV13 serotypes remain persistent in Canadian adults hospitalized with CAP, and represent between 5 and 10% of all CAP in this patient population.
最近的研究表明,13 价肺炎球菌结合疫苗(PCV13)对 65 岁以上健康成年人的 PCV13 型侵袭性肺炎球菌病(IPD)和肺炎球菌社区获得性肺炎(CAP)具有有效性,这促使许多国家重新评估成人免疫接种。在加拿大,鉴于自 2010 年以来引入的 PCV13 儿童免疫接种带来的预期群体免疫力,成人 PCV13 免疫接种的潜在益处尚不清楚。本研究描述了 2010 年至 2015 年期间,加拿大≥16 岁因 CAP 和 IPD 住院的成年人的血清型分布和临床结局。
在加拿大五个省份的成人医院进行 CAP 和 IPD 的主动监测。当从无菌部位分离出肺炎链球菌时,确定为 IPD。通过血液培养、痰培养或 PCV13 特异性尿抗原检测(UAD)分别确定菌血症和非菌血症性 CAP。通过胶乳反应、PCR 或 UAD 确定血清型。
在进行检测的 6687 例 CAP 病例中,肺炎链球菌阳性率从 2011 年的 15.9%降至 2014 年的 8.8%,但在 2015 年上升至 12.9%。PCV13 血清型引起的 CAP 也呈现出类似的趋势,从 2010 年的 8.3%降至 2014 年的 4.6%,但在 2015 年上升至 6.3%。这种下降主要归因于血清型 7F 和 19A,而比例增加则归因于血清型 3。菌血症性和非菌血症性 CAP 也呈现出类似的趋势。30 天死亡率、重症监护病房(ICU)入院率和机械通气需求等严重结局在 CAP 和 IPD 病例中较为突出,但在研究期间并未改变。
主要由血清型 7F 和 19A 引起的群体免疫力似乎部分被血清型 3 的比例增加所掩盖。尽管有群体免疫力的证据,但这些 PCV13 血清型在加拿大因 CAP 住院的成年人中仍然存在,占该患者人群中所有 CAP 的 5%至 10%。