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重组水疱性口炎病毒载体埃博拉疫苗(rVSV-ZEBOV)用于人道主义卫生工作者预防埃博拉病毒病的可行性和安全性:一项观察性研究

Feasibility and safety of rVSV-ZEBOV vaccination of humanitarian health workers against Ebola virus disease: an observational study.

作者信息

Carnino Luisa, Vetter Pauline, Peyraud Nicolas, Aebischer-Perone Sigiriya, Chappuis François, Huttner Angela, Kaiser Laurent, Eperon Gilles

机构信息

Division of Tropical and Humanitarian Medicine, Geneva University Hospitals, Rue Gabrielle-Perret-Gentil 6, Geneva 1205, Switzerland.

University of Geneva, Rue Michel-Servet 1, Geneva 1205, Switzerland.

出版信息

J Travel Med. 2021 Dec 29;28(8). doi: 10.1093/jtm/taab086.

Abstract

BACKGROUND AND RATIONALE

Geneva University Hospitals were granted a temporary authorization to administer the recombinant live vesicular stomatitis virus rVSV-ZEBOV (Ervebo®) vaccine to expatriate humanitarian frontline workers (FLWs) prior to mission deployment.

OBJECTIVES

Our aims were to assess the feasibility of FLW vaccination before deployment and to report adverse events (AEs).

METHODS

FLWs received a single injection of rVSV-ZEBOV (>7.2E7 plaque forming unit) during their pre-deployment medical check-up at the Travel Medicine Clinic of the Geneva University Hospitals (Day 0). A safety questionnaire regarding potential AEs was emailed to FLWs on Days 3 and 21. Early and delayed AEs were those starting within 3 or 21 days of vaccination, respectively.

RESULTS

Between 1 August 2019 and 30 June 2020, 124 FLWs received the rVSV-ZEBOV vaccine. Eighty-six volunteers (86/124; 69%) received a concomitant vaccine. The response rate to the follow-up questionnaire was 88 and 55% at Days 3 and 21, respectively. Most respondents (105/109; 96.3%), experienced at least one AE, with a mean of three (±SD 1.75) AEs per person. The most common AE was injection site pain, followed by fever (53/109; 48.6%), fatigue (51/109; 46.7%) and myalgia (49/109; 44.9%). Most early AEs (360/377; 95.4%) resolved within 3 days, reflecting vaccine reactogenicity. Delayed AEs were reported by 6/69 (7.2%) subjects, the median time to symptom onset was 11 days (range: 5-14); half of them were joint-related AEs (3/6). Four serious adverse events (SAE) were observed: two cases of high grade fever, one rash and one case of arthritis. Two suspected unexpected serious adverse reactions were observed: one case of continuing recurrent transient dizziness and fatigue considered related to the vaccine; and one case of presbyopia that was deemed unrelated.

CONCLUSION

AEs to rVSV-ZEBOV were common but in general transient and were well tolerated, pre-deployment rVSV-ZEBOV vaccination in FLW is feasible and can be included with pre-mission check-up.

摘要

背景与理论依据

日内瓦大学医院获得临时授权,可在海外人道主义一线工作者(FLW)任务部署前为其接种重组活水疱性口炎病毒rVSV-ZEBOV(Ervebo®)疫苗。

目的

我们的目标是评估在部署前为一线工作者接种疫苗的可行性,并报告不良事件(AE)。

方法

一线工作者在日内瓦大学医院旅行医学诊所进行部署前体检时(第0天)接受单次注射rVSV-ZEBOV(>7.2E7蚀斑形成单位)。在第3天和第21天,通过电子邮件向一线工作者发送关于潜在不良事件的安全调查问卷。早期和延迟不良事件分别是指在接种疫苗后3天或21天内开始出现的不良事件。

结果

在2019年8月1日至2020年6月30日期间,124名一线工作者接种了rVSV-ZEBOV疫苗。86名志愿者(86/124;69%)同时接种了其他疫苗。在第3天和第21天,对随访问卷的回复率分别为88%和55%。大多数受访者(105/109;96.3%)经历了至少一次不良事件,每人平均经历三次(±标准差1.75)不良事件。最常见的不良事件是注射部位疼痛,其次是发热(53/109;48.6%)、疲劳(51/109;46.7%)和肌痛(49/109;44.9%)。大多数早期不良事件(360/377;95.4%)在3天内缓解,反映了疫苗的反应原性。6/69(7.2%)的受试者报告了延迟不良事件,症状出现的中位时间为11天(范围:5 - 14天);其中一半是与关节相关的不良事件(3/6)。观察到4例严重不良事件(SAE):2例高热、1例皮疹和1例关节炎。观察到2例疑似意外严重不良反应:1例持续反复短暂头晕和疲劳被认为与疫苗有关;1例老花眼被认为无关。

结论

rVSV-ZEBOV疫苗的不良事件很常见,但一般是短暂的,耐受性良好,在一线工作者中部署前接种rVSV-ZEBOV疫苗是可行的,可纳入任务前检查。

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