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2018-2019 年刚果民主共和国埃博拉病毒病疫情期间 rVSV-ZEBOV 疫苗接种的效果:一项回顾性病例对照研究。

Effectiveness of rVSV-ZEBOV vaccination during the 2018-20 Ebola virus disease epidemic in the Democratic Republic of the Congo: a retrospective test-negative study.

机构信息

Epicentre, Paris, France.

General Direction of Disease Control, Ministry of Public Health, Hygiene, and Prevention, Kinshasa, Democratic Republic of the Congo.

出版信息

Lancet Infect Dis. 2024 Dec;24(12):1357-1365. doi: 10.1016/S1473-3099(24)00419-5. Epub 2024 Aug 20.

Abstract

BACKGROUND

The recombinant vesicular stomatitis virus-Zaire Ebola virus (rVSV-ZEBOV) vaccine is the only WHO prequalified vaccine recommended for use to respond to outbreaks of Ebola virus (species Zaire ebolavirus) by WHO's Strategic Advisory Group of Experts on Immunization. Despite the vaccine's widespread use during several outbreaks, no real-world effectiveness estimates are currently available in the literature.

METHODS

We conducted a retrospective test-negative analysis to estimate effectiveness of rVSV-ZEBOV vaccination against Ebola virus disease during the 2018-20 epidemic in the Democratic Republic of the Congo, using data on suspected Ebola virus disease cases collected from Ebola treatment centres. Those eligible for inclusion had an available Ebola virus RT-PCR result, available key data, were eligible for vaccination during the outbreak, and had symptom onset aligning with the period in which a ring-vaccination protocol was in use. After imputing missing data, each individual confirmed by RT-PCR to be Ebola virus disease-positive (defined as a case) was matched to one individual negative for Ebola virus disease (control) by sex, age, health zone, and month of symptom onset. Effectiveness was estimated from the odds ratio of being vaccinated (≥10 days before symptom onset) versus being unvaccinated among cases and controls, after adjusting for the matching factors. The imputation, matching and effectiveness estimation, was repeated 500 times.

FINDINGS

1273 (4·8%) of 26 438 eligible individuals were positive for Ebola virus disease (cases) and 25 165 (95·2%) were negative (controls). 40 (3·1%) cases and 1271 (5·1%) controls were reported as being vaccinated at least 10 days before symptom onset. After selecting individuals who reported exposure to an individual with Ebola virus disease within the 21 days before symptom onset and matching, the analysis datasets comprised a median of 309 cases and 309 controls. 10 days or more after vaccination, the effectiveness of rVSV-ZEBOV against Ebola virus disease was estimated to be 84% (95% credible interval 70-92).

INTERPRETATION

This analysis is the first to provide estimates of the real-world effectiveness of the rVSV-ZEBOV vaccine against Ebola virus disease, amid the widespread use of the vaccine during a large Ebola virus disease outbreak. Our findings confirm that rVSV-ZEBOV is highly protective against Ebola virus disease and support its use during outbreaks, even in challenging contexts such as in the eastern Democratic Republic of the Congo.

FUNDING

Médecins Sans Frontières.

TRANSLATION

For the French translation of the abstract see Supplementary Materials section.

摘要

背景

重组水疱性口炎病毒-扎伊尔埃博拉病毒(rVSV-ZEBOV)疫苗是世界卫生组织(WHO)唯一推荐的疫苗,用于应对由世界卫生组织免疫战略咨询专家组(SAGE)推荐使用的扎伊尔埃博拉病毒(埃博拉病毒属)暴发。尽管该疫苗在几次暴发中得到了广泛应用,但目前文献中尚无其实效的真实世界评估。

方法

我们采用回顾性病例对照研究,利用从埃博拉治疗中心收集的疑似埃博拉病毒病病例数据,对刚果民主共和国 2018-2019 年埃博拉疫情期间 rVSV-ZEBOV 疫苗接种对埃博拉病毒病的有效性进行评估。符合纳入标准的病例应具有可用的埃博拉病毒 RT-PCR 结果、关键数据可用、在暴发期间有资格接种疫苗且症状发作与环接种方案实施期间相吻合。在对缺失数据进行插补后,通过 RT-PCR 确认的每一例埃博拉病毒病阳性(定义为病例)都与一例埃博拉病毒病阴性(对照)个体按性别、年龄、卫生区和症状发作月份进行匹配。在调整匹配因素后,根据病例和对照中接种(症状发作前≥10 天)与未接种的比值,计算疫苗的有效性。该插补、匹配和有效性估计重复进行了 500 次。

结果

26438 名符合条件的个体中,有 1273 名(4.8%)埃博拉病毒病阳性(病例),25165 名(95.2%)埃博拉病毒病阴性(对照)。40 例(3.1%)病例和 1271 例(5.1%)对照报告在症状发作前至少 10 天接种了疫苗。在选择报告在症状发作前 21 天内接触过埃博拉病毒病患者的个体并进行匹配后,分析数据集中包括 309 例病例和 309 例对照。在接种后 10 天或更长时间,rVSV-ZEBOV 对埃博拉病毒病的有效性估计为 84%(95%置信区间 70-92)。

结论

这是首次在大规模埃博拉病毒病暴发期间广泛使用该疫苗的情况下,提供 rVSV-ZEBOV 疫苗对埃博拉病毒病真实世界有效性的评估。我们的研究结果证实,rVSV-ZEBOV 对埃博拉病毒病具有高度保护作用,并支持在暴发期间使用该疫苗,即使在刚果民主共和国东部等具有挑战性的环境中也是如此。

资助

无国界医生组织。

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