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Immunoinformatic Execution and Design of an Anti-Epstein–Barr Virus Vaccine with Multiple Epitopes Triggering Innate and Adaptive Immune Responses
One of the most important breakthroughs in healthcare is the development of vaccines. The life cycle and its gene expression in the numerous virus-associated disorders must be considered when choosing the target vaccine antigen for Epstein–Barr virus (EBV). The vaccine candidate used in the current...
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/PMC10609278/ https://www.ncbi.nlm.nih.gov/pubmed/37894106 http://dx.doi.org/10.3390/microorganisms11102448 |
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author | Ahmed, Naveed Rabaan, Ali A. Alwashmi, Ameen S. S. Albayat, Hawra Mashraqi, Mutaib M. Alshehri, Ahmad A. Garout, Mohammed Abduljabbar, Wesam A. Yusof, Nik Yusnoraini Yean, Chan Yean |
author_facet | Ahmed, Naveed Rabaan, Ali A. Alwashmi, Ameen S. S. Albayat, Hawra Mashraqi, Mutaib M. Alshehri, Ahmad A. Garout, Mohammed Abduljabbar, Wesam A. Yusof, Nik Yusnoraini Yean, Chan Yean |
author_sort | Ahmed, Naveed |
collection | PubMed |
description | One of the most important breakthroughs in healthcare is the development of vaccines. The life cycle and its gene expression in the numerous virus-associated disorders must be considered when choosing the target vaccine antigen for Epstein–Barr virus (EBV). The vaccine candidate used in the current study will also be effective against all other herpesvirus strains, based on the conservancy study, which verified that the protein is present in all herpesviruses. From the screening, two B-cell epitopes, four MHC-I, and five MHC-II restricted epitopes were chosen for further study. The refined epitopes indicated 70.59% coverage of the population in Malaysia and 93.98% worldwide. After removing the one toxin (PADRE) from the original vaccine design, it was projected that the new vaccine would not be similar to the human host and would instead be antigenic, immunogenic, non-allergenic, and non-toxic. The vaccine construct was stable, thermostable, soluble, and hydrophilic. The immunological simulation projected that the vaccine candidate would be subject to a long-lasting active adaptive response and a short-lived active innate response. With IgM concentrations of up to 450 cells per mm(3) and active B-cell concentrations of up to 400 cells per mm(3), the B-cells remain active for a considerable time. The construct also discovered other conformational epitopes, improving its ability to stimulate an immune response. This suggests that, upon injection, the epitope will target the B-cell surface receptors and elicit a potent immune response. Furthermore, the discotope analysis confirmed that our conformational B-cell epitope was not displaced during the design. Lastly, the docking complex was stable and exhibited little deformability under heat pressure. These computational results are very encouraging for future testing of our proposed vaccine, which may potentially help in the management and prevention of EBV infections worldwide. |
format | Online Article Text |
id | pubmed-10609278 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-106092782023-10-28 Immunoinformatic Execution and Design of an Anti-Epstein–Barr Virus Vaccine with Multiple Epitopes Triggering Innate and Adaptive Immune Responses Ahmed, Naveed Rabaan, Ali A. Alwashmi, Ameen S. S. Albayat, Hawra Mashraqi, Mutaib M. Alshehri, Ahmad A. Garout, Mohammed Abduljabbar, Wesam A. Yusof, Nik Yusnoraini Yean, Chan Yean Microorganisms Article One of the most important breakthroughs in healthcare is the development of vaccines. The life cycle and its gene expression in the numerous virus-associated disorders must be considered when choosing the target vaccine antigen for Epstein–Barr virus (EBV). The vaccine candidate used in the current study will also be effective against all other herpesvirus strains, based on the conservancy study, which verified that the protein is present in all herpesviruses. From the screening, two B-cell epitopes, four MHC-I, and five MHC-II restricted epitopes were chosen for further study. The refined epitopes indicated 70.59% coverage of the population in Malaysia and 93.98% worldwide. After removing the one toxin (PADRE) from the original vaccine design, it was projected that the new vaccine would not be similar to the human host and would instead be antigenic, immunogenic, non-allergenic, and non-toxic. The vaccine construct was stable, thermostable, soluble, and hydrophilic. The immunological simulation projected that the vaccine candidate would be subject to a long-lasting active adaptive response and a short-lived active innate response. With IgM concentrations of up to 450 cells per mm(3) and active B-cell concentrations of up to 400 cells per mm(3), the B-cells remain active for a considerable time. The construct also discovered other conformational epitopes, improving its ability to stimulate an immune response. This suggests that, upon injection, the epitope will target the B-cell surface receptors and elicit a potent immune response. Furthermore, the discotope analysis confirmed that our conformational B-cell epitope was not displaced during the design. Lastly, the docking complex was stable and exhibited little deformability under heat pressure. These computational results are very encouraging for future testing of our proposed vaccine, which may potentially help in the management and prevention of EBV infections worldwide. MDPI 2023-09-29 /pmc/articles/PMC10609278/ /pubmed/37894106 http://dx.doi.org/10.3390/microorganisms11102448 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 Ahmed, Naveed Rabaan, Ali A. Alwashmi, Ameen S. S. Albayat, Hawra Mashraqi, Mutaib M. Alshehri, Ahmad A. Garout, Mohammed Abduljabbar, Wesam A. Yusof, Nik Yusnoraini Yean, Chan Yean Immunoinformatic Execution and Design of an Anti-Epstein–Barr Virus Vaccine with Multiple Epitopes Triggering Innate and Adaptive Immune Responses |
title | Immunoinformatic Execution and Design of an Anti-Epstein–Barr Virus Vaccine with Multiple Epitopes Triggering Innate and Adaptive Immune Responses |
title_full | Immunoinformatic Execution and Design of an Anti-Epstein–Barr Virus Vaccine with Multiple Epitopes Triggering Innate and Adaptive Immune Responses |
title_fullStr | Immunoinformatic Execution and Design of an Anti-Epstein–Barr Virus Vaccine with Multiple Epitopes Triggering Innate and Adaptive Immune Responses |
title_full_unstemmed | Immunoinformatic Execution and Design of an Anti-Epstein–Barr Virus Vaccine with Multiple Epitopes Triggering Innate and Adaptive Immune Responses |
title_short | Immunoinformatic Execution and Design of an Anti-Epstein–Barr Virus Vaccine with Multiple Epitopes Triggering Innate and Adaptive Immune Responses |
title_sort | immunoinformatic execution and design of an anti-epstein–barr virus vaccine with multiple epitopes triggering innate and adaptive immune responses |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10609278/ https://www.ncbi.nlm.nih.gov/pubmed/37894106 http://dx.doi.org/10.3390/microorganisms11102448 |
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