Dissecting humoral immune responses to an MVA-vectored MERS-CoV vaccine in humans using a systems serology approach
- iScience. 2024 Jul 8;27(8):110470. doi: 10.1016/j.isci.2024.110470.
- 1. Institute for Infection Research and Vaccine Development (IIRVD), Center for Internal Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
- 2. Department for Clinical Immunology of Infectious Diseases, Bernhard Nocht Institute for Tropical Medicine, Hamburg, Germany.
- 3. German Center for Infection Research, Partner Site Hamburg-Lübeck-Borstel-Riems, Hamburg, Germany.
- 4. Department of Obstetrics and Fetal Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
- 5. Glyco-HAM, a Cooperation of Universität Hamburg, Technology Platform Mass Spectrometry and University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
- 6. University of Bordeaux, INSERM, INRIA, BPH, U1219, Sistm, Bordeaux, France.
- 7. Vaccine Research Institute, Creteil, France.
- 8. Department of Viroscience, Erasmus University Medical Center, Rotterdam, the Netherlands.
- 9. Antibiotic Stewardship Team, Pharmacy of the University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
- 10. Institute of Virology, Philipps University Marburg, Marburg, Germany.
- 11. German Center for Infection Research, Partner Site Gießen-Marburg-Langen, Marburg, Germany.
- 12. Division of Virology, Department of Veterinary Sciences, Ludwig Maximilian University Munich, Munich, Germany.
- 13. German Center for Infection Research, Partner Site München, Munich, Germany.
- 14. CHU de Bordeaux, Service d'Information Médicale, Bordeaux, France.
- 15. Division of Infectious Diseases, 1st Department of Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Besides neutralizing antibodies, which are considered an important measure for vaccine immunogenicity, Fc-mediated antibody functions can contribute to antibody-mediated protection. They are strongly influenced by structural antibody properties such as subclass and Fc glycan composition. We here applied a systems serology approach to dissect humoral immune responses induced by MVA-MERS-S, an MVA-vectored vaccine against the Middle East respiratory syndrome coronavirus (MERS-CoV). Building on preceding studies reporting the safety and immunogenicity of MVA-MERS-S, our study highlights the potential of a late boost, administered one year after prime, to enhance both neutralizing and Fc-mediated antibody functionality compared to the primary vaccination series. Distinct characteristics were observed for antibodies specific to the MERS-CoV spike protein S1 and S2 subunits, regarding subclass and glycan compositions as well as Fc functionality. These findings highlight the benefit of a late homologous booster vaccination with MVA-MERS-S and may be of interest for the design of future coronavirus vaccines.
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