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Design and Immunogenicity of SARS-CoV-2 DNA Vaccine Encoding RBD-PVXCP Fusion Protein
The potential of immune-evasive mutation accumulation in the SARS-CoV-2 virus has led to its rapid spread, causing over 600 million confirmed cases and more than 6.5 million confirmed deaths. The huge demand for the rapid development and deployment of low-cost and effective vaccines against emerging...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10300735/ https://www.ncbi.nlm.nih.gov/pubmed/37376403 http://dx.doi.org/10.3390/vaccines11061014 |
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author | Dormeshkin, Dmitri Katsin, Mikalai Stegantseva, Maria Golenchenko, Sergey Shapira, Michail Dubovik, Simon Lutskovich, Dzmitry Kavaleuski, Anton Meleshko, Alexander |
author_facet | Dormeshkin, Dmitri Katsin, Mikalai Stegantseva, Maria Golenchenko, Sergey Shapira, Michail Dubovik, Simon Lutskovich, Dzmitry Kavaleuski, Anton Meleshko, Alexander |
author_sort | Dormeshkin, Dmitri |
collection | PubMed |
description | The potential of immune-evasive mutation accumulation in the SARS-CoV-2 virus has led to its rapid spread, causing over 600 million confirmed cases and more than 6.5 million confirmed deaths. The huge demand for the rapid development and deployment of low-cost and effective vaccines against emerging variants has renewed interest in DNA vaccine technology. Here, we report the rapid generation and immunological evaluation of novel DNA vaccine candidates against the Wuhan-Hu-1 and Omicron variants based on the RBD protein fused with the Potato virus X coat protein (PVXCP). The delivery of DNA vaccines using electroporation in a two-dose regimen induced high-antibody titers and profound cellular responses in mice. The antibody titers induced against the Omicron variant of the vaccine were sufficient for effective protection against both Omicron and Wuhan-Hu-1 virus infections. The PVXCP protein in the vaccine construct shifted the immune response to the favorable Th1-like type and provided the oligomerization of RBD-PVXCP protein. Naked DNA delivery by needle-free injection allowed us to achieve antibody titers comparable with mRNA-LNP delivery in rabbits. These data identify the RBD-PVXCP DNA vaccine platform as a promising solution for robust and effective SARS-CoV-2 protection, supporting further translational study. |
format | Online Article Text |
id | pubmed-10300735 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-103007352023-06-29 Design and Immunogenicity of SARS-CoV-2 DNA Vaccine Encoding RBD-PVXCP Fusion Protein Dormeshkin, Dmitri Katsin, Mikalai Stegantseva, Maria Golenchenko, Sergey Shapira, Michail Dubovik, Simon Lutskovich, Dzmitry Kavaleuski, Anton Meleshko, Alexander Vaccines (Basel) Article The potential of immune-evasive mutation accumulation in the SARS-CoV-2 virus has led to its rapid spread, causing over 600 million confirmed cases and more than 6.5 million confirmed deaths. The huge demand for the rapid development and deployment of low-cost and effective vaccines against emerging variants has renewed interest in DNA vaccine technology. Here, we report the rapid generation and immunological evaluation of novel DNA vaccine candidates against the Wuhan-Hu-1 and Omicron variants based on the RBD protein fused with the Potato virus X coat protein (PVXCP). The delivery of DNA vaccines using electroporation in a two-dose regimen induced high-antibody titers and profound cellular responses in mice. The antibody titers induced against the Omicron variant of the vaccine were sufficient for effective protection against both Omicron and Wuhan-Hu-1 virus infections. The PVXCP protein in the vaccine construct shifted the immune response to the favorable Th1-like type and provided the oligomerization of RBD-PVXCP protein. Naked DNA delivery by needle-free injection allowed us to achieve antibody titers comparable with mRNA-LNP delivery in rabbits. These data identify the RBD-PVXCP DNA vaccine platform as a promising solution for robust and effective SARS-CoV-2 protection, supporting further translational study. MDPI 2023-05-23 /pmc/articles/PMC10300735/ /pubmed/37376403 http://dx.doi.org/10.3390/vaccines11061014 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Dormeshkin, Dmitri Katsin, Mikalai Stegantseva, Maria Golenchenko, Sergey Shapira, Michail Dubovik, Simon Lutskovich, Dzmitry Kavaleuski, Anton Meleshko, Alexander Design and Immunogenicity of SARS-CoV-2 DNA Vaccine Encoding RBD-PVXCP Fusion Protein |
title | Design and Immunogenicity of SARS-CoV-2 DNA Vaccine Encoding RBD-PVXCP Fusion Protein |
title_full | Design and Immunogenicity of SARS-CoV-2 DNA Vaccine Encoding RBD-PVXCP Fusion Protein |
title_fullStr | Design and Immunogenicity of SARS-CoV-2 DNA Vaccine Encoding RBD-PVXCP Fusion Protein |
title_full_unstemmed | Design and Immunogenicity of SARS-CoV-2 DNA Vaccine Encoding RBD-PVXCP Fusion Protein |
title_short | Design and Immunogenicity of SARS-CoV-2 DNA Vaccine Encoding RBD-PVXCP Fusion Protein |
title_sort | design and immunogenicity of sars-cov-2 dna vaccine encoding rbd-pvxcp fusion protein |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10300735/ https://www.ncbi.nlm.nih.gov/pubmed/37376403 http://dx.doi.org/10.3390/vaccines11061014 |
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