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Virus-Like Particles Are Efficient Tools for Boosting mRNA-Induced Antibodies
Anne-Cathrine S Vogt1,2, Lukas Jörg3,4, Byron Martina5,6
1Department of Rheumatology and Immunology, University Hospital, Bern, Switzerland.
Heterologous prime-boost vaccination using mRNA and virus-like particle (VLP) vaccines elicits superior antibody responses against COVID-19. This strategy offers an optimized approach for vaccine efficacy and cost-effectiveness.
Area of Science:
- Immunology
- Vaccinology
- Virology
Background:
- Messenger RNA (mRNA) vaccines have been highly effective against COVID-19.
- Emerging SARS-CoV-2 variants of concern (VoCs) necessitate strategies to maintain robust antibody responses.
- Heterologous prime-boost vaccination is being explored to enhance vaccine efficacy, address supply issues, and improve safety.
Purpose of the Study:
- To investigate antibody responses induced by heterologous prime-boost vaccination strategies for COVID-19.
- To compare antibody responses between homologous and heterologous prime-boost regimens using mRNA and virus-like particle (VLP) vaccines.
- To evaluate the potential of heterologous prime-boost strategies for optimizing vaccine efficacy and economics.
Main Methods:
- Utilized the VLP-based mCuMVTT-RBM vaccine candidate and the approved mRNA-1273 vaccine.
- Administered homologous prime-boost regimens (mRNA-mRNA or VLP-VLP).
- Administered heterologous prime-boost regimens (mRNA-VLP or VLP-mRNA).
Main Results:
- Homologous prime-boost regimens with either mRNA or VLP vaccines induced high levels of high avidity antibodies.
- Heterologous prime-boost regimens, regardless of the order (mRNA-VLP or VLP-mRNA), induced optimal antibody responses.
- These findings suggest enhanced immunogenicity with mixed vaccine platforms.
Conclusions:
- Heterologous prime-boost vaccination strategies can optimize COVID-19 vaccine efficacy.
- Combining mRNA and VLP vaccine platforms offers a promising approach for improved immune responses.
- This strategy holds potential for enhancing the economic viability of novel vaccine development.
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