Escobar-Ziede Pía, Borras-Bermejo Blanca, Pinós-Tella Laia, Vivet-Escalé Martí, Peñalver-Piñol Arnau, Martinez Judith, Rodrigo-Pendás Jose-Ángel, García-Pérez Jorge, Álvarez-López Patricia, Nadal-Baron Patricia, Antón Andrés, Parés-Badell Oleguer
Servei de Medicina Preventiva i Epidemiologia, Vall d'Hebron Hospital Universitari, Vall d'Hebron Barcelona Hospital Campus, Passeig Vall d'Hebron 119-129, 08035 Barcelona, Spain; Grup de recerca d'Epidemiologia i Salut Pública, Vall d'Hebron Institut de Recerca (VHIR), Vall d'Hebron Hospital Universitari, Vall d'Hebron Barcelona Hospital Campus, Passeig Vall d'Hebron 119-129, 08035 Barcelona, Spain.
Servei de Medicina Preventiva i Epidemiologia, Vall d'Hebron Hospital Universitari, Vall d'Hebron Barcelona Hospital Campus, Passeig Vall d'Hebron 119-129, 08035 Barcelona, Spain; Grup de recerca d'Epidemiologia i Salut Pública, Vall d'Hebron Institut de Recerca (VHIR), Vall d'Hebron Hospital Universitari, Vall d'Hebron Barcelona Hospital Campus, Passeig Vall d'Hebron 119-129, 08035 Barcelona, Spain; Unitat Docent Vall d'Hebron, Universitat Autònoma de Barcelona, Passeig Vall d'Hebron 119-129, 08035 Barcelona, Spain.
Vaccine. 2025 Jun 20;59:127295. doi: 10.1016/j.vaccine.2025.127295. Epub 2025 May 27.
Mpox is a viral illness for which the MVA-BN vaccine was authorized during the 2022 global outbreak. Although initial studies reported high immunogenicity, real-world evidence on vaccine effectiveness (VE) remains scarce. This study aimed to estimate the real-world VE of at least one dose of the MVA-BN vaccine against symptomatic mpox in adults tested at a tertiary hospital in Barcelona, Spain.
We conducted a test-negative case-control study between July 2022 and December 2023. Adults tested for mpox by PCR were included. Cases were PCR-positive; controls were PCR-negative. Vaccine effectiveness of at least one dose was calculated as (1 - adjusted odds ratio) × 100 %, using multivariable logistic regression.
Among 301 participants, 126 were cases and 175 controls. Crude VE of ≥1 dose ≥14 days before testing was 47 % (95 % CI: -17 % to 77 %). After adjusting for sex, age, testing center, sexually transmitted infection (STI) testing in the last year and risk criteria for mpox VE increased to 74 % (95 % CI: 38 % to 90 %) but decreased to 44 % (95 % CI: -52 % to 79 %) when additionally adjusting for epidemiological weeks. Similar patterns were observed in a subgroup of men with at least one risk criteria for mpox.
Our study provides context-specific evidence on the effectiveness of a single MVA-BN vaccine dose against symptomatic mpox in a real-world setting. Vaccine effectiveness estimates varied depending on adjustment strategy, highlighting the importance of accounting for epidemiological weeks to avoid overestimation.
猴痘是一种病毒性疾病,在2022年全球疫情期间,MVA-BN疫苗被批准用于该病。尽管初步研究报告显示其具有高免疫原性,但关于疫苗有效性(VE)的真实世界证据仍然匮乏。本研究旨在评估在西班牙巴塞罗那一家三级医院接受检测的成年人中,至少一剂MVA-BN疫苗针对有症状猴痘的真实世界VE。
我们在2022年7月至2023年12月期间开展了一项检测阴性病例对照研究。纳入通过PCR检测猴痘的成年人。病例为PCR阳性;对照为PCR阴性。使用多变量逻辑回归,将至少一剂疫苗的有效性计算为(1 - 调整后的比值比)×100%。
在301名参与者中,126例为病例,175例为对照。检测前≥14天接种≥1剂疫苗的粗VE为47%(95%CI:-17%至77%)。在调整性别、年龄、检测中心、过去一年的性传播感染(STI)检测以及猴痘风险标准后,VE升至74%(95%CI:38%至90%),但在进一步调整流行周后降至44%(95%CI:-52%至79%)。在有至少一项猴痘风险标准的男性亚组中观察到类似模式。
我们研究提供了在真实世界环境中,单剂MVA-BN疫苗针对有症状猴痘有效性的特定背景证据。疫苗有效性估计值因调整策略而异,突出了考虑流行周以避免高估的重要性。