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Peer reviewedOpen accessInfluenzaMonkeypoxSmallpox

Low levels of monkeypox virus-neutralizing antibodies after MVA-BN vaccination in healthy individuals

Nature Medicine·

Luca M. Zaeck, Mart M. Lamers, Babs E. Verstrepen, Theo M. Bestebroer, Martin E. van Royen, Hannelore Götz, Marc C. Shamier, Leanne P. M. van Leeuwen, Katharina S. Schmitz, Kimberley Alblas, Suzanne van Efferen, Susanne Bogers, Sandra Scherbeijn, Guus F. Rimmelzwaan, Eric C. M. van Gorp, Marion P. G. Koopmans, Bart L. Haagmans, Corine H. GeurtsvanKessel, Rory D. de Vries

DOI
10.1038/s41591-022-02090-w
PMID
36257333
PMCID
PMC9873555
OpenAlex
W4306721676
Study type
Journal article
Publisher
Springer Science and Business Media LLC
Article type
journal-article
Integrity
current

Why this research matters now

These observations address knowledge gaps surrounding authorized MVA-BN deployment during a recently declared international health emergency by quantifying early immune responses.

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Structured evidence summary

Research question

The study evaluates whether the MVA-BN vaccine generates measurable monkeypox virus-neutralizing antibodies in healthy adults without prior poxvirus exposure.

Study design

This research conducts an immunological comparison of antibody titers across multiple vaccination protocols, including a standard two-dose series, a reduced-dose approach, and a subsequent booster administration.

Population and setting

The analysis centers on healthy participants lacking previous viral priming, though precise demographic or geographic characteristics are not detailed in the provided metadata.

Main findings

A conventional two-dose MVA-BN regimen yielded comparatively modest neutralizing antibody concentrations in unexposed individuals. Introducing a third dose substantially elevated these measurements, whereas a fractionated dosing strategy produced lower values. The clinical relevance of these immune markers remains undetermined.

Public-health relevance

These observations address knowledge gaps surrounding authorized MVA-BN deployment during a recently declared international health emergency by quantifying early immune responses.

Important limitations

The provided text lacks explicit methodological constraints or sample size disclosures. Therefore, this summary depends entirely on the supplied abstract and bibliographic records, requiring access to the complete manuscript for rigorous appraisal. Furthermore, the investigation tracks laboratory immune markers rather than direct disease prevention outcomes.

GIDS interpretation

This record contributes foundational immunogenicity data pertinent to orthopoxvirus preparedness literature. Its classification under vaccination and outbreak investigation categories indicates potential utility for scholars monitoring historical vaccine performance metrics during recent zoonotic periods.

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Related GIDS surveillance

Literature context does not validate, explain, or change a surveillance signal. Exact and contextual relationships are shown separately.

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Evidence relationships

This article has 11 auditable classifier relationships to diseases, places, topics, and study design.

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