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A Novel Probiotic-Based Oral Vaccine against SARS-CoV-2 Omicron Variant B.1.1.529
COVID-19 pandemic, caused by the SARS-CoV-2 virus, is still affecting the entire world via the rapid emergence of new contagious variants. Vaccination remains the most effective prevention strategy for viral infection, yet not all countries have sufficient access to vaccines due to limitations in ma...
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/PMC10530581/ https://www.ncbi.nlm.nih.gov/pubmed/37762235 http://dx.doi.org/10.3390/ijms241813931 |
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author | Chau, Eddie Chung Ting Kwong, Tsz Ching Pang, Chun Keung Chan, Lee Tung Chan, Andrew Man Lok Yao, Xiaoqiang Tam, John Siu Lun Chan, Shun Wan Leung, George Pak Heng Tai, William Chi Shing Kwan, Yiu Wa |
author_facet | Chau, Eddie Chung Ting Kwong, Tsz Ching Pang, Chun Keung Chan, Lee Tung Chan, Andrew Man Lok Yao, Xiaoqiang Tam, John Siu Lun Chan, Shun Wan Leung, George Pak Heng Tai, William Chi Shing Kwan, Yiu Wa |
author_sort | Chau, Eddie Chung Ting |
collection | PubMed |
description | COVID-19 pandemic, caused by the SARS-CoV-2 virus, is still affecting the entire world via the rapid emergence of new contagious variants. Vaccination remains the most effective prevention strategy for viral infection, yet not all countries have sufficient access to vaccines due to limitations in manufacturing and transportation. Thus, there is an urgent need to develop an easy-to-use, safe, and low-cost vaccination approach. Genetically modified microorganisms, especially probiotics, are now commonly recognized as attractive vehicles for delivering bioactive molecules via oral and mucosal routes. In this study, Lactobacillus casei has been selected as the oral vaccine candidate based on its’ natural immunoadjuvant properties and the ability to resist acidic gastric environment, to express antigens of SARS-CoV-2 Omicron variant B.1.1.529 with B-cell and T-cell epitopes. This newly developed vaccine, OMGVac, was shown to elicit a robust IgG systemic immune response against the spike protein of Omicron variant B.1.1.529 in Golden Syrian hamsters. No adverse effects were found throughout this study, and the overall safety was evaluated in terms of physiological and histopathological examinations of different organs harvested. In addition, this study illustrated the use of the recombinant probiotic as a live delivery vector in the initiation of systemic immunity, which shed light on the future development of next-generation vaccines to combat emerging infectious diseases. |
format | Online Article Text |
id | pubmed-10530581 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-105305812023-09-28 A Novel Probiotic-Based Oral Vaccine against SARS-CoV-2 Omicron Variant B.1.1.529 Chau, Eddie Chung Ting Kwong, Tsz Ching Pang, Chun Keung Chan, Lee Tung Chan, Andrew Man Lok Yao, Xiaoqiang Tam, John Siu Lun Chan, Shun Wan Leung, George Pak Heng Tai, William Chi Shing Kwan, Yiu Wa Int J Mol Sci Article COVID-19 pandemic, caused by the SARS-CoV-2 virus, is still affecting the entire world via the rapid emergence of new contagious variants. Vaccination remains the most effective prevention strategy for viral infection, yet not all countries have sufficient access to vaccines due to limitations in manufacturing and transportation. Thus, there is an urgent need to develop an easy-to-use, safe, and low-cost vaccination approach. Genetically modified microorganisms, especially probiotics, are now commonly recognized as attractive vehicles for delivering bioactive molecules via oral and mucosal routes. In this study, Lactobacillus casei has been selected as the oral vaccine candidate based on its’ natural immunoadjuvant properties and the ability to resist acidic gastric environment, to express antigens of SARS-CoV-2 Omicron variant B.1.1.529 with B-cell and T-cell epitopes. This newly developed vaccine, OMGVac, was shown to elicit a robust IgG systemic immune response against the spike protein of Omicron variant B.1.1.529 in Golden Syrian hamsters. No adverse effects were found throughout this study, and the overall safety was evaluated in terms of physiological and histopathological examinations of different organs harvested. In addition, this study illustrated the use of the recombinant probiotic as a live delivery vector in the initiation of systemic immunity, which shed light on the future development of next-generation vaccines to combat emerging infectious diseases. MDPI 2023-09-11 /pmc/articles/PMC10530581/ /pubmed/37762235 http://dx.doi.org/10.3390/ijms241813931 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 Chau, Eddie Chung Ting Kwong, Tsz Ching Pang, Chun Keung Chan, Lee Tung Chan, Andrew Man Lok Yao, Xiaoqiang Tam, John Siu Lun Chan, Shun Wan Leung, George Pak Heng Tai, William Chi Shing Kwan, Yiu Wa A Novel Probiotic-Based Oral Vaccine against SARS-CoV-2 Omicron Variant B.1.1.529 |
title | A Novel Probiotic-Based Oral Vaccine against SARS-CoV-2 Omicron Variant B.1.1.529 |
title_full | A Novel Probiotic-Based Oral Vaccine against SARS-CoV-2 Omicron Variant B.1.1.529 |
title_fullStr | A Novel Probiotic-Based Oral Vaccine against SARS-CoV-2 Omicron Variant B.1.1.529 |
title_full_unstemmed | A Novel Probiotic-Based Oral Vaccine against SARS-CoV-2 Omicron Variant B.1.1.529 |
title_short | A Novel Probiotic-Based Oral Vaccine against SARS-CoV-2 Omicron Variant B.1.1.529 |
title_sort | novel probiotic-based oral vaccine against sars-cov-2 omicron variant b.1.1.529 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10530581/ https://www.ncbi.nlm.nih.gov/pubmed/37762235 http://dx.doi.org/10.3390/ijms241813931 |
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