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Design of a multi-epitope vaccine against cervical cancer using immunoinformatics approaches

Cervical cancer, caused by human papillomavirus (HPV), is the fourth most common type of cancer among women worldwide. While HPV prophylactic vaccines are available, they have no therapeutic effects and do not clear up existing infections. This study aims to design a therapeutic vaccine against cerv...

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Autores principales: Sanami, Samira, Azadegan-Dehkordi, Fatemeh, Rafieian-Kopaei, Mahmoud, Salehi, Majid, Ghasemi-Dehnoo, Maryam, Mahooti, Mehran, Alizadeh, Morteza, Bagheri, Nader
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8196015/
https://www.ncbi.nlm.nih.gov/pubmed/34117331
http://dx.doi.org/10.1038/s41598-021-91997-4
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author Sanami, Samira
Azadegan-Dehkordi, Fatemeh
Rafieian-Kopaei, Mahmoud
Salehi, Majid
Ghasemi-Dehnoo, Maryam
Mahooti, Mehran
Alizadeh, Morteza
Bagheri, Nader
author_facet Sanami, Samira
Azadegan-Dehkordi, Fatemeh
Rafieian-Kopaei, Mahmoud
Salehi, Majid
Ghasemi-Dehnoo, Maryam
Mahooti, Mehran
Alizadeh, Morteza
Bagheri, Nader
author_sort Sanami, Samira
collection PubMed
description Cervical cancer, caused by human papillomavirus (HPV), is the fourth most common type of cancer among women worldwide. While HPV prophylactic vaccines are available, they have no therapeutic effects and do not clear up existing infections. This study aims to design a therapeutic vaccine against cervical cancer using reverse vaccinology. In this study, the E6 and E7 oncoproteins from HPV16 were chosen as the target antigens for epitope prediction. Cytotoxic T lymphocytes (CTL) and helper T lymphocytes (HTL) epitopes were predicted, and the best epitopes were selected based on antigenicity, allergenicity, and toxicity. The final vaccine construct was composed of the selected epitopes, along with the appropriate adjuvant and linkers. The multi-epitope vaccine was evaluated in terms of physicochemical properties, antigenicity, and allergenicity. The tertiary structure of the vaccine construct was predicted. Furthermore, several analyses were also carried out, including molecular docking, molecular dynamics (MD) simulation, and in silico cloning of the vaccine construct. The results showed that the final proposed vaccine could be considered an effective therapeutic vaccine for HPV; however, in vitro and in vivo experiments are required to validate the efficacy of this vaccine candidate.
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spelling pubmed-81960152021-06-15 Design of a multi-epitope vaccine against cervical cancer using immunoinformatics approaches Sanami, Samira Azadegan-Dehkordi, Fatemeh Rafieian-Kopaei, Mahmoud Salehi, Majid Ghasemi-Dehnoo, Maryam Mahooti, Mehran Alizadeh, Morteza Bagheri, Nader Sci Rep Article Cervical cancer, caused by human papillomavirus (HPV), is the fourth most common type of cancer among women worldwide. While HPV prophylactic vaccines are available, they have no therapeutic effects and do not clear up existing infections. This study aims to design a therapeutic vaccine against cervical cancer using reverse vaccinology. In this study, the E6 and E7 oncoproteins from HPV16 were chosen as the target antigens for epitope prediction. Cytotoxic T lymphocytes (CTL) and helper T lymphocytes (HTL) epitopes were predicted, and the best epitopes were selected based on antigenicity, allergenicity, and toxicity. The final vaccine construct was composed of the selected epitopes, along with the appropriate adjuvant and linkers. The multi-epitope vaccine was evaluated in terms of physicochemical properties, antigenicity, and allergenicity. The tertiary structure of the vaccine construct was predicted. Furthermore, several analyses were also carried out, including molecular docking, molecular dynamics (MD) simulation, and in silico cloning of the vaccine construct. The results showed that the final proposed vaccine could be considered an effective therapeutic vaccine for HPV; however, in vitro and in vivo experiments are required to validate the efficacy of this vaccine candidate. Nature Publishing Group UK 2021-06-11 /pmc/articles/PMC8196015/ /pubmed/34117331 http://dx.doi.org/10.1038/s41598-021-91997-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Sanami, Samira
Azadegan-Dehkordi, Fatemeh
Rafieian-Kopaei, Mahmoud
Salehi, Majid
Ghasemi-Dehnoo, Maryam
Mahooti, Mehran
Alizadeh, Morteza
Bagheri, Nader
Design of a multi-epitope vaccine against cervical cancer using immunoinformatics approaches
title Design of a multi-epitope vaccine against cervical cancer using immunoinformatics approaches
title_full Design of a multi-epitope vaccine against cervical cancer using immunoinformatics approaches
title_fullStr Design of a multi-epitope vaccine against cervical cancer using immunoinformatics approaches
title_full_unstemmed Design of a multi-epitope vaccine against cervical cancer using immunoinformatics approaches
title_short Design of a multi-epitope vaccine against cervical cancer using immunoinformatics approaches
title_sort design of a multi-epitope vaccine against cervical cancer using immunoinformatics approaches
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8196015/
https://www.ncbi.nlm.nih.gov/pubmed/34117331
http://dx.doi.org/10.1038/s41598-021-91997-4
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