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Immunogenicity of High-Dose MVA-Based MERS Vaccine Candidate in Mice and Camels
Naif Khalaf Alharbi1,2, Fahad Aljamaan3, Haya A Aljami1
1Vaccine Development Unit, King Abdullah International Medical Research Center, Riyadh 11481, Saudi Arabia.
Abstract:
The Middle East respiratory syndrome coronavirus (MERS-CoV) is a zoonotic pathogen that can transmit from dromedary camels to humans, causing severe pneumonia, with a 35% mortality rate. Vaccine candidates have been developed and tested in mice, camels, and humans. Previously, we developed a vaccine based on the modified vaccinia virus Ankara (MVA) viral vector, encoding a full-length spike protein of MERS-CoV, MVA-MERS. Here, we report the immunogenicity of high-dose MVA-MERS in prime-boost vaccinations in mice and camels.
Methods:
Three groups of mice were immunised with MVA wild-type (MVA-wt) and MVA-MERS (MVA-wt/MVA-MERS), MVA-MERS/MVA-wt, or MVA-MERS/MVA-MERS. Camels were immunised with two doses of PBS, MVA-wt, or MVA-MERS. Antibody (Ab) responses were evaluated using ELISA and MERS pseudovirus neutralisation assays.
Results:
Two high doses of MVA-MERS induced strong Ab responses in both mice and camels, including neutralising antibodies. Anti-MVA Ab responses did not affect the immune responses to the vaccine antigen (MERS-CoV spike).
Conclusions:
MVA-MERS vaccine, administered in a homologous prime-boost regimen, induced high levels of neutralising anti-MERS-CoV antibodies in mice and camels. This could be considered for further development and evaluation as a dromedary vaccine to reduce MERS-CoV transmission to humans.
Insights
A modified vaccinia virus Ankara (MVA) vaccine expressing the MERS-CoV spike protein (MVA-MERS) generated strong neutralizing antibody responses in mice and camels. This MVA-MERS vaccine shows promise for reducing Middle East respiratory syndrome coronavirus transmission.
Area of Science:
- Virology
- Immunology
- Vaccinology
Background:
- Middle East respiratory syndrome coronavirus (MERS-CoV) is a zoonotic virus transmitted from dromedary camels to humans, causing severe pneumonia with a high mortality rate.
- Developing effective vaccines is crucial to mitigate MERS-CoV spread and impact.
- A modified vaccinia virus Ankara (MVA) vector vaccine, MVA-MERS, encoding the full-length MERS-CoV spike protein has been previously developed.
Purpose of the Study:
- To evaluate the immunogenicity of a high-dose MVA-MERS vaccine administered via prime-boost regimens in mice and camels.
- To assess the induction of antibody responses, including neutralizing antibodies, against MERS-CoV.
Main Methods:
- Mice were immunized using prime-boost strategies with MVA-wild-type (MVA-wt) and MVA-MERS.
- Camels received two doses of either phosphate-buffered saline (PBS), MVA-wt, or MVA-MERS.
- Antibody responses were quantified using ELISA and MERS pseudovirus neutralization assays.
Main Results:
- Homologous prime-boost vaccination with two high doses of MVA-MERS elicited robust antibody responses in both mice and camels.
- The induced antibodies demonstrated significant neutralizing activity against MERS-CoV.
- Pre-existing or induced anti-MVA antibodies did not impede the immune response to the MERS-CoV spike antigen.
Conclusions:
- The MVA-MERS vaccine, when administered in a homologous prime-boost regimen, effectively induces high levels of neutralizing anti-MERS-CoV antibodies in mice and camels.
- These findings support the further development of MVA-MERS as a potential vaccine for dromedary camels to reduce human MERS-CoV transmission.
- Targeting dromedary camels offers a One Health approach to control zoonotic disease spread.
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