Mason Lauren M K, Betancur Estefania, Riera-Montes Margarita, Lienert Florian, Scheele Suzanne
P95 Epidemiology and Pharmacovigilance, Leuven, Belgium.
Bavarian Nordic Switzerland AG, Zug, Switzerland.
Vaccine. 2024 Dec 2;42(26):126409. doi: 10.1016/j.vaccine.2024.126409. Epub 2024 Oct 16.
Mpox is a disease endemic to Central and West Africa. It caused outbreaks in non-endemic countries, mainly in 2022. The endemic Democratic Republic of Congo is currently experiencing its largest outbreak yet. The vaccine Modified Vaccinia Ankara-Bavarian Nordic (MVA-BN) is approved for active immunization against mpox and smallpox. Since the outbreak in 2022, real-world studies have assessed MVA-BN's vaccine effectiveness (VE) against mpox, and this systematic literature review aims to summarize the most current evidence.
Medline (via PubMed), Embase, and LILACS were searched, as well as grey literature sources and publications' bibliographies to identify observational studies published between 1/Jan/2022 and 28/Feb/2024 that estimate the VE of MVA-BN against mpox or provide risk measures that allow calculation of these VE estimates. Data were presented descriptively in tables and text; the methodological quality of included records was assessed using NHLBI/NIH quality assessment tools.
The literature search identified 16 records that fit the inclusion criteria. The studies took place in high-income countries and were heterogeneous in design, setting, and definition of at-risk populations. MVA-BN VE estimates against mpox infection were assessed. Where the study population was exclusively or primarily those receiving pre-exposure prophylactic vaccination, the adjusted VE estimates ranged from 35 % to 86 % (n = 8 studies) for one dose and from 66 % to 90 % (n = 5) for two doses. Where only post-exposure prophylactic vaccination was assessed, adjusted VE estimates were reported for one dose only at 78 % and 89 % (n = 2). Additionally, MVA-BN reduced the risk of mpox-related hospitalization in one study and the severity of mpox clinical manifestations in two studies.
Despite heterogeneity in study design, setting, and at-risk populations, the reported VE estimates against mpox infection demonstrated the effectiveness of one or two doses of MVA-BN in the context of an outbreak across multiple countries.
猴痘是中非和西非的地方病。它在非流行国家引发了疫情,主要是在2022年。地方病流行的刚果民主共和国目前正在经历其有史以来最大规模的疫情。改良安卡拉痘苗病毒-巴伐利亚北欧公司(MVA-BN)疫苗被批准用于主动免疫预防猴痘和天花。自2022年疫情爆发以来,真实世界研究评估了MVA-BN疫苗对猴痘的有效性(VE),本系统文献综述旨在总结最新证据。
检索了医学文献数据库(通过PubMed)、Embase和拉丁美洲及加勒比地区卫生科学数据库(LILACS),以及灰色文献来源和出版物的参考文献,以识别2022年1月1日至2024年2月28日期间发表的观察性研究,这些研究估计了MVA-BN对猴痘的疫苗有效性,或提供了可用于计算这些疫苗有效性估计值的风险测量指标。数据以表格和文字形式进行描述性呈现;使用美国国立卫生研究院心肺血液研究所(NHLBI)/美国国立卫生研究院(NIH)质量评估工具评估纳入记录的方法学质量。
文献检索确定了16条符合纳入标准的记录。这些研究在高收入国家进行,在设计、研究背景和高危人群定义方面存在异质性。评估了MVA-BN对猴痘感染的疫苗有效性估计值。如果研究人群完全是或主要是接受暴露前预防性疫苗接种的人群,一剂疫苗的调整后疫苗有效性估计值在35%至86%之间(n = 8项研究),两剂疫苗的调整后疫苗有效性估计值在66%至90%之间(n = 5项研究)。如果仅评估暴露后预防性疫苗接种,仅报告了一剂疫苗的调整后疫苗有效性估计值,分别为78%和89%(n = 2项研究)。此外,在一项研究中,MVA-BN降低了与猴痘相关的住院风险,在两项研究中降低了猴痘临床表现的严重程度。
尽管在研究设计、研究背景和高危人群方面存在异质性,但报告的针对猴痘感染的疫苗有效性估计值证明了一剂或两剂MVA-BN在多个国家爆发疫情的情况下的有效性。