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Developing an Effective Peptide-Based Vaccine for COVID-19: Preliminary Studies in Mice Models
Coronavirus disease 2019 (COVID-19) has caused massive health and economic disasters worldwide. Although several vaccines have effectively slowed the spread of the virus, their long-term protection and effectiveness against viral variants are still uncertain. To address these potential shortcomings,...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8954996/ https://www.ncbi.nlm.nih.gov/pubmed/35336856 http://dx.doi.org/10.3390/v14030449 |
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author | Yang, Haiqiang Cao, Jessica Lin, Xiaoyang Yue, Jingwen Zieneldien, Tarek Kim, Janice Wang, Lianchun Fang, Jianmin Huang, Ruo-Pan Bai, Yun Sneed, Kevin Cao, Chuanhai |
author_facet | Yang, Haiqiang Cao, Jessica Lin, Xiaoyang Yue, Jingwen Zieneldien, Tarek Kim, Janice Wang, Lianchun Fang, Jianmin Huang, Ruo-Pan Bai, Yun Sneed, Kevin Cao, Chuanhai |
author_sort | Yang, Haiqiang |
collection | PubMed |
description | Coronavirus disease 2019 (COVID-19) has caused massive health and economic disasters worldwide. Although several vaccines have effectively slowed the spread of the virus, their long-term protection and effectiveness against viral variants are still uncertain. To address these potential shortcomings, this study proposes a peptide-based vaccine to prevent COVID-19. A total of 15 B cell epitopes of the wild-type severe acute respiratory coronavirus 2 (SARS-CoV-2) spike (S) protein were selected, and their HLA affinities predicted in silico. Peptides were divided into two groups and tested in C57BL/6 mice with either QS21 or Al(OH)(3) as the adjuvant. Our results demonstrated that the peptide-based vaccine stimulated high and durable antibody responses in mice, with the T and B cell responses differing based on the type of adjuvant employed. Using epitope mapping, we showed that our peptide-based vaccine produced antibody patterns similar to those in COVID-19 convalescent individuals. Moreover, plasma from vaccinated mice and recovered COVID-19 humans had the same neutralizing activity when tested with a pseudo particle assay. Our data indicate that this adjuvant peptide-based vaccine can generate sustainable and effective B and T cell responses. Thus, we believe that our peptide-based vaccine can be a safe and effective vaccine against COVID-19, particularly because of the flexibility of including new peptides to prevent emerging SARS-CoV-2 variants and avoiding unwanted autoimmune responses. |
format | Online Article Text |
id | pubmed-8954996 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-89549962022-03-26 Developing an Effective Peptide-Based Vaccine for COVID-19: Preliminary Studies in Mice Models Yang, Haiqiang Cao, Jessica Lin, Xiaoyang Yue, Jingwen Zieneldien, Tarek Kim, Janice Wang, Lianchun Fang, Jianmin Huang, Ruo-Pan Bai, Yun Sneed, Kevin Cao, Chuanhai Viruses Article Coronavirus disease 2019 (COVID-19) has caused massive health and economic disasters worldwide. Although several vaccines have effectively slowed the spread of the virus, their long-term protection and effectiveness against viral variants are still uncertain. To address these potential shortcomings, this study proposes a peptide-based vaccine to prevent COVID-19. A total of 15 B cell epitopes of the wild-type severe acute respiratory coronavirus 2 (SARS-CoV-2) spike (S) protein were selected, and their HLA affinities predicted in silico. Peptides were divided into two groups and tested in C57BL/6 mice with either QS21 or Al(OH)(3) as the adjuvant. Our results demonstrated that the peptide-based vaccine stimulated high and durable antibody responses in mice, with the T and B cell responses differing based on the type of adjuvant employed. Using epitope mapping, we showed that our peptide-based vaccine produced antibody patterns similar to those in COVID-19 convalescent individuals. Moreover, plasma from vaccinated mice and recovered COVID-19 humans had the same neutralizing activity when tested with a pseudo particle assay. Our data indicate that this adjuvant peptide-based vaccine can generate sustainable and effective B and T cell responses. Thus, we believe that our peptide-based vaccine can be a safe and effective vaccine against COVID-19, particularly because of the flexibility of including new peptides to prevent emerging SARS-CoV-2 variants and avoiding unwanted autoimmune responses. MDPI 2022-02-22 /pmc/articles/PMC8954996/ /pubmed/35336856 http://dx.doi.org/10.3390/v14030449 Text en © 2022 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 Yang, Haiqiang Cao, Jessica Lin, Xiaoyang Yue, Jingwen Zieneldien, Tarek Kim, Janice Wang, Lianchun Fang, Jianmin Huang, Ruo-Pan Bai, Yun Sneed, Kevin Cao, Chuanhai Developing an Effective Peptide-Based Vaccine for COVID-19: Preliminary Studies in Mice Models |
title | Developing an Effective Peptide-Based Vaccine for COVID-19: Preliminary Studies in Mice Models |
title_full | Developing an Effective Peptide-Based Vaccine for COVID-19: Preliminary Studies in Mice Models |
title_fullStr | Developing an Effective Peptide-Based Vaccine for COVID-19: Preliminary Studies in Mice Models |
title_full_unstemmed | Developing an Effective Peptide-Based Vaccine for COVID-19: Preliminary Studies in Mice Models |
title_short | Developing an Effective Peptide-Based Vaccine for COVID-19: Preliminary Studies in Mice Models |
title_sort | developing an effective peptide-based vaccine for covid-19: preliminary studies in mice models |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8954996/ https://www.ncbi.nlm.nih.gov/pubmed/35336856 http://dx.doi.org/10.3390/v14030449 |
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