Preprint Article Version 1 This version is not peer-reviewed

Reactogenicity and immunogenicity against MPXV of the intradermal administration of Modified Vaccinia Ankara compared to the standard subcutaneous route

Version 1 : Received: 6 November 2024 / Approved: 7 November 2024 / Online: 8 November 2024 (13:56:39 CET)

How to cite: Mazzotta, V.; Piselli, P.; Cozzi Lepri, A.; Matusali, G.; Cimini, E.; Esvan, R.; Colavita, F.; Gagliardini, R.; Notari, S.; Oliva, A.; Meschi, S.; Casetti, R.; Micheli, G.; Bordi, L.; Giacinta, A.; Grassi, G.; Gebremeskel Tekle, S.; Cimaglia, C.; Paulicelli, J.; Caioli, A.; Gallì, P.; Duca, G. D.; Lichtner, M.; Sarmati, L.; Tamburrini, E.; Mastroianni, C.; Latini, A.; Faccendini, P.; Fontana, C.; Nicastri, E.; Siddu, A.; Barca, A.; Vaia, F.; Girardi, E.; Maggi, F.; Antinori, A. Reactogenicity and immunogenicity against MPXV of the intradermal administration of Modified Vaccinia Ankara compared to the standard subcutaneous route. Preprints 2024, 2024110546. https://doi.org/10.20944/preprints202411.0546.v1 Mazzotta, V.; Piselli, P.; Cozzi Lepri, A.; Matusali, G.; Cimini, E.; Esvan, R.; Colavita, F.; Gagliardini, R.; Notari, S.; Oliva, A.; Meschi, S.; Casetti, R.; Micheli, G.; Bordi, L.; Giacinta, A.; Grassi, G.; Gebremeskel Tekle, S.; Cimaglia, C.; Paulicelli, J.; Caioli, A.; Gallì, P.; Duca, G. D.; Lichtner, M.; Sarmati, L.; Tamburrini, E.; Mastroianni, C.; Latini, A.; Faccendini, P.; Fontana, C.; Nicastri, E.; Siddu, A.; Barca, A.; Vaia, F.; Girardi, E.; Maggi, F.; Antinori, A. Reactogenicity and immunogenicity against MPXV of the intradermal administration of Modified Vaccinia Ankara compared to the standard subcutaneous route. Preprints 2024, 2024110546. https://doi.org/10.20944/preprints202411.0546.v1

Abstract

The recent resurgence of Mpox in central Africa has been declared again a Public Health Emergency of International Concern (PHEIC) requiring coordinated international responses. Vaccination is a priority to expand protection and enhance control strategies, but the vaccine's need exceeds the currently available doses. Intradermal (ID) administration of one-fifth of the standard Modified-Vaccinia-Ankara (MVA-BN) dose was temporarily authorized during the 2022 PHEIC. Studies conducted before 2022 provided evidence about the humoral response against the Vaccinia virus (VACV) after vaccination but not against the Mpox virus (MPXV). Moreover, no data are available on the T-cell response elicited by MVA-BN administered subcutaneously or intradermally. Here, we compare the two vaccine administration routes according to reactogenicity (using data of n=943 vaccine recipients) and immunogenicity (n=225 vaccine recipients) attending INMI Spallanzani hospital during the 2022 vaccination campaign in Rome, Italy. We found that the ID route elicited higher titers of MPXV-specific IgG (mean difference of 0.26 log2, p=0.05) and nAbs (0.24 log2, p=0.08) than the subcutaneous (SC) route one month after the complete vaccination cycle. At the same time, no evidence for a difference in cellular response was found. MVA-BN was globally well tolerated despite higher reactogenicity for the ID than the SC route, especially for the reactions at the local injection site. The ID dose-sparing strategy was proven safe and immunogenic and would make vaccination available to more people. Our data support the current WHO recommendation of using the ID route in in low-medium income countries (LMIC) although response data in people infected with the new 1b clade are urgently needed.

Keywords

mpox; Immunogenicity; Reactogenicity; Cellular response; Humoral response; Vaccine; MVA-BN; Trial emulation.

Subject

Medicine and Pharmacology, Epidemiology and Infectious Diseases

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