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Cell host & microbe · 2023

Complement-dependent mpox-virus-neutralizing antibodies in infected and vaccinated individuals.

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Hubert Mathieu, Guivel-Benhassine Florence, Bruel Timothée, Porrot Françoise, Planas Delphine, Vanhomwegen Jessica, Wiedemann Aurélie, Burrel Sonia, Marot Stéphane, Palich Romain, Monsel Gentiane, Diombera Harouna, Gallien Sébastien, Lopez-Zaragoza Jose Luis, Vindrios William, Taieb Fabien, Fernandes-Pellerin Sandrine, Delhaye Maurine, Laude Hélène, Arowas Laurence, Ungeheuer Marie-Noelle, Hocqueloux Laurent, Pourcher Valérie, Prazuck Thierry, Marcelin Anne-Geneviève, Lelièvre Jean-Daniel, Batéjat Christophe, Lévy Yves, Manuguerra Jean-Claude, Schwartz Olivier

Аннотация

Mpox virus (MPXV) caused a multi-country outbreak in non-endemic areas in 2022. Following historic success of smallpox vaccination with vaccinia virus (VACV)-based vaccines, the third generation modified vaccinia Ankara (MVA)-based vaccine was used as prophylaxis for MPXV, but its effectiveness remains poorly characterized. Here, we applied two assays to quantify neutralizing antibodies (NAbs) in sera from control, MPXV-infected, or MVA-vaccinated individuals. Various levels of MVA NAbs were detected after infection, historic smallpox, or recent MVA vaccination. MPXV was minimally sensitive to neutralization. However, addition of complement enhanced detection of responsive individuals and NAb levels. Anti-MVA and -MPXV NAbs were observed in 94% and 82% of infected individuals, respectively, and 92% and 56% of MVA vaccinees, respectively. NAb titers were higher in individuals born before 1980, highlighting the impact of historic smallpox vaccination on humoral immunity. Altogether, our results indicate that MPXV neutralization is complement dependent and uncover mechanisms underlying vaccine effectiveness.

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