Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Dormeshkin, Dmitri, Katsin, Mikalai, Stegantseva, Maria, Golenchenko, Sergey, Shapira, Michail, Dubovik, Simon, Lutskovich, Dzmitry, Kavaleuski, Anton, Meleshko, Alexander
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
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
_version_ 1785064646719307776
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
work_keys_str_mv AT dormeshkindmitri designandimmunogenicityofsarscov2dnavaccineencodingrbdpvxcpfusionprotein
AT katsinmikalai designandimmunogenicityofsarscov2dnavaccineencodingrbdpvxcpfusionprotein
AT stegantsevamaria designandimmunogenicityofsarscov2dnavaccineencodingrbdpvxcpfusionprotein
AT golenchenkosergey designandimmunogenicityofsarscov2dnavaccineencodingrbdpvxcpfusionprotein
AT shapiramichail designandimmunogenicityofsarscov2dnavaccineencodingrbdpvxcpfusionprotein
AT duboviksimon designandimmunogenicityofsarscov2dnavaccineencodingrbdpvxcpfusionprotein
AT lutskovichdzmitry designandimmunogenicityofsarscov2dnavaccineencodingrbdpvxcpfusionprotein
AT kavaleuskianton designandimmunogenicityofsarscov2dnavaccineencodingrbdpvxcpfusionprotein
AT meleshkoalexander designandimmunogenicityofsarscov2dnavaccineencodingrbdpvxcpfusionprotein