Lindstrand Ann, Kalyango Joan, Alfvén Tobias, Darenberg Jessica, Kadobera Daniel, Bwanga Freddie, Peterson Stefan, Henriques-Normark Birgitta, Källander Karin
Department of Public Health Sciences, Karolinska Institutet, Stockholm, Sweden.
Public Health Agency of Sweden, Stockholm, Sweden.
PLoS One. 2016 Nov 9;11(11):e0166018. doi: 10.1371/journal.pone.0166018. eCollection 2016.
Pneumonia is the major cause of death in children globally, with more than 900,000 deaths annually in children under five years of age. Streptococcus pneumoniae causes most deaths, most often in the form of community acquired pneumonia. Pneumococcal conjugate vaccines (PCVs) are currently being implemented in many low-income countries. PCVs decrease vaccine-type pneumococcal carriage, a prerequisite for invasive pneumococcal disease, and thereby affects pneumococcal disease and transmission. In Uganda, PCV was launched in 2014, but baseline data is lacking for pneumococcal serotypes in carriage.
To study pneumococcal nasopharyngeal carriage and serotype distribution in children under 5 years of age prior to PCV introduction in Uganda.
Three cross-sectional pneumococcal carriage surveys were conducted in 2008, 2009 and 2011, comprising respectively 150, 587 and 1024 randomly selected children aged less than five years from the Iganga/Mayuge Health and Demographic Surveillance Site. The caretakers were interviewed about illness history of the child and 1723 nasopharyngeal specimens were collected. From these, 927 isolates of S. pneumoniae were serotyped.
Overall, the carriage rate of S. pneumoniae was 56% (957/1723). Pneumococcal carriage was associated with illness on the day of the interview (OR = 1.50, p = 0.04). The most common pneumococcal serotypes were in descending order 19F (16%), 23F (9%), 6A (8%), 29 (7%) and 6B (7%). One percent of the strains were non-typeable. The potential serotype coverage rate for PCV10 was 42% and 54% for PCV13.
About half of circulating pneumococcal serotypes in carriage in the Ugandan under-five population studied was covered by available PCVs.
肺炎是全球儿童死亡的主要原因,五岁以下儿童每年有超过90万例死亡。肺炎链球菌导致了大多数死亡,最常见的形式是社区获得性肺炎。肺炎球菌结合疫苗(PCV)目前正在许多低收入国家推行。PCV可降低疫苗型肺炎球菌携带率,而这是侵袭性肺炎球菌疾病的一个前提条件,从而影响肺炎球菌疾病及传播。在乌干达,PCV于2014年推出,但缺乏关于携带的肺炎球菌血清型的基线数据。
研究在乌干达引入PCV之前五岁以下儿童的肺炎球菌鼻咽部携带情况及血清型分布。
在2008年、2009年和2011年进行了三项横断面肺炎球菌携带情况调查,分别从伊甘加/马尤盖健康与人口监测点随机选取了150名、587名和1024名五岁以下儿童。对看护人就儿童的疾病史进行了访谈,并收集了1723份鼻咽部标本。从中对927株肺炎链球菌分离株进行了血清分型。
总体而言,肺炎链球菌的携带率为56%(957/1723)。肺炎球菌携带与访谈当天的疾病有关(比值比=1.50,p=0.04)。最常见的肺炎球菌血清型按降序排列为19F(16%)、23F(9%)、6A(8%)、29(7%)和6B(7%)。1%的菌株无法分型。PCV10的潜在血清型覆盖率为42%,PCV13为54%。
在所研究的乌干达五岁以下人群中,携带的循环肺炎球菌血清型约有一半可被现有PCV覆盖。