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

Abstract 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 aga...

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Autores principales: Samira Sanami, Fatemeh Azadegan-Dehkordi, Mahmoud Rafieian-Kopaei, Majid Salehi, Maryam Ghasemi-Dehnoo, Mehran Mahooti, Morteza Alizadeh, Nader Bagheri
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Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/2872f49638ee41a9b6d96c22f9350fa5
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spelling oai:doaj.org-article:2872f49638ee41a9b6d96c22f9350fa52021-12-02T17:47:15ZDesign of a multi-epitope vaccine against cervical cancer using immunoinformatics approaches10.1038/s41598-021-91997-42045-2322https://doaj.org/article/2872f49638ee41a9b6d96c22f9350fa52021-06-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-91997-4https://doaj.org/toc/2045-2322Abstract 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.Samira SanamiFatemeh Azadegan-DehkordiMahmoud Rafieian-KopaeiMajid SalehiMaryam Ghasemi-DehnooMehran MahootiMorteza AlizadehNader BagheriNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-15 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Samira Sanami
Fatemeh Azadegan-Dehkordi
Mahmoud Rafieian-Kopaei
Majid Salehi
Maryam Ghasemi-Dehnoo
Mehran Mahooti
Morteza Alizadeh
Nader Bagheri
Design of a multi-epitope vaccine against cervical cancer using immunoinformatics approaches
description Abstract 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.
format article
author Samira Sanami
Fatemeh Azadegan-Dehkordi
Mahmoud Rafieian-Kopaei
Majid Salehi
Maryam Ghasemi-Dehnoo
Mehran Mahooti
Morteza Alizadeh
Nader Bagheri
author_facet Samira Sanami
Fatemeh Azadegan-Dehkordi
Mahmoud Rafieian-Kopaei
Majid Salehi
Maryam Ghasemi-Dehnoo
Mehran Mahooti
Morteza Alizadeh
Nader Bagheri
author_sort Samira Sanami
title 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_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_sort design of a multi-epitope vaccine against cervical cancer using immunoinformatics approaches
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/2872f49638ee41a9b6d96c22f9350fa5
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