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七价结合肺炎球菌疫苗在美国印第安儿童中的疗效和安全性:群组随机试验

Efficacy and safety of seven-valent conjugate pneumococcal vaccine in American Indian children: group randomised trial.

作者信息

O'Brien Katherine L, Moulton Lawrence H, Reid Raymond, Weatherholtz Robert, Oski Jane, Brown Laura, Kumar Gaurav, Parkinson Alan, Hu Diana, Hackell Jill, Chang Ih, Kohberger Robert, Siber George, Santosham Mathuram

机构信息

Center for American Indian Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA.

出版信息

Lancet. 2003 Aug 2;362(9381):355-61. doi: 10.1016/S0140-6736(03)14022-6.

Abstract

BACKGROUND

Streptococcus pneumoniae is the main cause of invasive bacterial disease in children aged younger than 2 years. Navajo and White Mountain Apache children have some of the highest rates of invasive pneumococcal disease documented in the world. We aimed to assess the safety and efficacy of a seven-valent polysaccharide protein conjugate pneumococcal vaccine (PnCRM7) against such disease.

METHODS

In a group-randomised study, we gave this vaccine to children younger than 2 years from the Navajo and White Mountain Apache Indian reservations; meningococcal type C conjugate vaccine (MnCC) served as the control vaccine. Vaccine schedules were determined by age at enrollment. We recorded episodes of invasive pneumococcal disease and serotyped isolates. Analyses were by intention to treat and per protocol.

FINDINGS

8292 children enrolled in the trial. In the per protocol analysis of the primary efficacy group (children enrolled by 7 months of age) there were eight cases of vaccine serotype disease in the controls and two in the PnCRM7 group; in the intention-to-treat analysis we noted 11 cases of vaccine serotype disease in the MnCC control group and two in the PnCRM7 group. After group randomisation had been controlled for, the per protocol primary efficacy of PnCRM7 was 76.8% (95% CI -9.4% to 95.1%) and the intention-to-treat total primary efficacy was 82.6% (21.4% to 96.1%).

INTERPRETATION

PnCRM7 vaccine prevents vaccine serotype invasive pneumococcal disease even in a high risk population. Other regions with similar disease burden should consider including this vaccine in the routine childhood vaccine schedule.

摘要

背景

肺炎链球菌是2岁以下儿童侵袭性细菌性疾病的主要病因。纳瓦霍族和白山阿帕契族儿童的侵袭性肺炎球菌疾病发病率是世界上有记录的最高发病率之一。我们旨在评估一种七价多糖蛋白结合肺炎球菌疫苗(PnCRM7)预防此类疾病的安全性和有效性。

方法

在一项群组随机研究中,我们给来自纳瓦霍族和白山阿帕契族印第安保留地的2岁以下儿童接种了这种疫苗;C群脑膜炎球菌结合疫苗(MnCC)作为对照疫苗。疫苗接种程序根据入组时的年龄确定。我们记录了侵袭性肺炎球菌疾病的发作情况,并对分离株进行了血清分型。分析采用意向性分析和符合方案分析。

结果

8292名儿童参与了该试验。在对主要疗效组(7个月龄前入组的儿童)的符合方案分析中,对照组有8例疫苗血清型疾病病例,PnCRM7组有2例;在意向性分析中,我们注意到MnCC对照组有11例疫苗血清型疾病病例,PnCRM7组有2例。在对群组随机化进行控制后,PnCRM7的符合方案主要疗效为76.8%(95%可信区间为 -9.4%至95.

1%),意向性分析的总体主要疗效为82.6%(21.4%至96.1%)。

解读

PnCRM7疫苗即使在高危人群中也能预防疫苗血清型侵袭性肺炎球菌疾病。其他具有类似疾病负担的地区应考虑将这种疫苗纳入儿童常规疫苗接种程序。

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