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Immunogenicity of candidate SARS-CoV-2 DNA vaccines based on the spike protein

Coronavirus disease 2019 caused by the novel human severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is currently a major threat to public health worldwide. To deal with the needs of vaccine, we developed four DNA vaccine candidates against SARS-CoV-2, based on the full-length spike (S) o...

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Autores principales: Lim, Heeji, Kim, Se Eun, Lee, Yun Ha, Hwang, Yun-Ho, Kim, Su Hwan, Kim, Mi Young, Chung, Gyung Tae, Kim, You-Jin, Kim, Dokeun, Lee, Jung-Ah
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Authors. Published by Elsevier Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9185170/
https://www.ncbi.nlm.nih.gov/pubmed/35751974
http://dx.doi.org/10.1016/j.virol.2022.06.006
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author Lim, Heeji
Kim, Se Eun
Lee, Yun Ha
Hwang, Yun-Ho
Kim, Su Hwan
Kim, Mi Young
Chung, Gyung Tae
Kim, You-Jin
Kim, Dokeun
Lee, Jung-Ah
author_facet Lim, Heeji
Kim, Se Eun
Lee, Yun Ha
Hwang, Yun-Ho
Kim, Su Hwan
Kim, Mi Young
Chung, Gyung Tae
Kim, You-Jin
Kim, Dokeun
Lee, Jung-Ah
author_sort Lim, Heeji
collection PubMed
description Coronavirus disease 2019 caused by the novel human severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is currently a major threat to public health worldwide. To deal with the needs of vaccine, we developed four DNA vaccine candidates against SARS-CoV-2, based on the full-length spike (S) or truncated S protein. Following mice vaccination, we measured T-cell response and antigen-specific neutralizing antibody (NAb) titer. All four candidates induced humoral immune responses, including elevated levels of total IgG and NAbs, and cell-mediated immune responses, including multiple cytokine expression. However, the full-length S DNA vaccine enhanced the immune responses most significantly. We then evaluated its appropriate antigen dose and vaccination schedule. Although all immunized groups showed higher immune response than the control group, inoculation with 50 μg antigen led to the highest NAb titer. Immunity was significantly increased after the third inoculation. Thus, the full-length S DNA vaccine can potentially prevent SARS-CoV-2 infection.
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spelling pubmed-91851702022-06-10 Immunogenicity of candidate SARS-CoV-2 DNA vaccines based on the spike protein Lim, Heeji Kim, Se Eun Lee, Yun Ha Hwang, Yun-Ho Kim, Su Hwan Kim, Mi Young Chung, Gyung Tae Kim, You-Jin Kim, Dokeun Lee, Jung-Ah Virology Brief Communication Coronavirus disease 2019 caused by the novel human severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is currently a major threat to public health worldwide. To deal with the needs of vaccine, we developed four DNA vaccine candidates against SARS-CoV-2, based on the full-length spike (S) or truncated S protein. Following mice vaccination, we measured T-cell response and antigen-specific neutralizing antibody (NAb) titer. All four candidates induced humoral immune responses, including elevated levels of total IgG and NAbs, and cell-mediated immune responses, including multiple cytokine expression. However, the full-length S DNA vaccine enhanced the immune responses most significantly. We then evaluated its appropriate antigen dose and vaccination schedule. Although all immunized groups showed higher immune response than the control group, inoculation with 50 μg antigen led to the highest NAb titer. Immunity was significantly increased after the third inoculation. Thus, the full-length S DNA vaccine can potentially prevent SARS-CoV-2 infection. The Authors. Published by Elsevier Inc. 2022-08 2022-06-10 /pmc/articles/PMC9185170/ /pubmed/35751974 http://dx.doi.org/10.1016/j.virol.2022.06.006 Text en © 2022 The Authors Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Brief Communication
Lim, Heeji
Kim, Se Eun
Lee, Yun Ha
Hwang, Yun-Ho
Kim, Su Hwan
Kim, Mi Young
Chung, Gyung Tae
Kim, You-Jin
Kim, Dokeun
Lee, Jung-Ah
Immunogenicity of candidate SARS-CoV-2 DNA vaccines based on the spike protein
title Immunogenicity of candidate SARS-CoV-2 DNA vaccines based on the spike protein
title_full Immunogenicity of candidate SARS-CoV-2 DNA vaccines based on the spike protein
title_fullStr Immunogenicity of candidate SARS-CoV-2 DNA vaccines based on the spike protein
title_full_unstemmed Immunogenicity of candidate SARS-CoV-2 DNA vaccines based on the spike protein
title_short Immunogenicity of candidate SARS-CoV-2 DNA vaccines based on the spike protein
title_sort immunogenicity of candidate sars-cov-2 dna vaccines based on the spike protein
topic Brief Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9185170/
https://www.ncbi.nlm.nih.gov/pubmed/35751974
http://dx.doi.org/10.1016/j.virol.2022.06.006
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