List of links used in this study.

<div><p>Significant progress has been made in <i>HIV-1</i> research; however, researchers have not yet achieved the objective of eradicating <i>HIV-1</i> infection. Accordingly, in this study, eucaryotic and procaryotic in silico vaccines were developed for <i&...

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Main Author: Ava Hashempour (11753878) (author)
Other Authors: Nastaran Khodadad (17535416) (author), Peyman Bemani (10651254) (author), Younes Ghasemi (3125685) (author), Shokufeh Akbarinia (17535419) (author), Reza Bordbari (19751532) (author), Amir Hossein Tabatabaei (19751535) (author), Shahab Falahi (18301765) (author)
Published: 2024
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_version_ 1852026315004182528
author Ava Hashempour (11753878)
author2 Nastaran Khodadad (17535416)
Peyman Bemani (10651254)
Younes Ghasemi (3125685)
Shokufeh Akbarinia (17535419)
Reza Bordbari (19751532)
Amir Hossein Tabatabaei (19751535)
Shahab Falahi (18301765)
author2_role author
author
author
author
author
author
author
author_facet Ava Hashempour (11753878)
Nastaran Khodadad (17535416)
Peyman Bemani (10651254)
Younes Ghasemi (3125685)
Shokufeh Akbarinia (17535419)
Reza Bordbari (19751532)
Amir Hossein Tabatabaei (19751535)
Shahab Falahi (18301765)
author_role author
dc.creator.none.fl_str_mv Ava Hashempour (11753878)
Nastaran Khodadad (17535416)
Peyman Bemani (10651254)
Younes Ghasemi (3125685)
Shokufeh Akbarinia (17535419)
Reza Bordbari (19751532)
Amir Hossein Tabatabaei (19751535)
Shahab Falahi (18301765)
dc.date.none.fl_str_mv 2024-09-27T17:36:27Z
dc.identifier.none.fl_str_mv 10.1371/journal.pone.0306559.t001
dc.relation.none.fl_str_mv https://figshare.com/articles/dataset/List_of_links_used_in_this_study_/27121440
dc.rights.none.fl_str_mv CC BY 4.0
info:eu-repo/semantics/openAccess
dc.subject.none.fl_str_mv Medicine
Microbiology
Molecular Biology
Biotechnology
Immunology
Cancer
Infectious Diseases
Virology
Biological Sciences not elsewhere classified
molecular dynamic stimulation
immunological simulation showed
div >< p
codon optimization ensured
simulate immune responses
strong binding affinities
human vaccine model
1 gag </
strong binding
gag </
1 </
consistent responses
human cells
e </
coli </
γ induction
yet achieved
world ’
vaccine models
vaccine formulated
successful translation
significant progress
reverse vaccinology
experimental verification
epitopes located
designed constructs
conserved domains
challenges faced
bcl epitopes
approximately 93
100 major
dc.title.none.fl_str_mv List of links used in this study.
dc.type.none.fl_str_mv Dataset
info:eu-repo/semantics/publishedVersion
dataset
description <div><p>Significant progress has been made in <i>HIV-1</i> research; however, researchers have not yet achieved the objective of eradicating <i>HIV-1</i> infection. Accordingly, in this study, eucaryotic and procaryotic in silico vaccines were developed for <i>HIV-Gag</i> polyproteins from 100 major <i>HIV</i> subtypes and CRFs using immunoinformatic techniques to simulate immune responses in mice and humans. The epitopes located in the conserved domains of the <i>Gag</i> polyprotein were evaluated for allergenicity, antigenicity, immunogenicity, toxicity, homology, topology, and IFN-γ induction. Adjuvants, linkers, CTLs, HTLs, and BCL epitopes were incorporated into the vaccine models. Strong binding affinities were detected between HLA/MHC alleles, TLR-2, TLR-3, TLR-4, TLR-7, and TLR-9, and vaccine models. Immunological simulation showed that innate and adaptive immune cells elicited active and consistent responses. The human vaccine model was matched with approximately 93.91% of the human population. The strong binding of the vaccine to MHC/HLA and TLR molecules was confirmed through molecular dynamic stimulation. Codon optimization ensured the successful translation of the designed constructs into human cells and <i>E</i>. <i>coli</i> hosts. We believe that the <i>HIV-1 Gag</i> vaccine formulated in our research can reduce the challenges faced in developing an <i>HIV-1</i> vaccine. Nevertheless, experimental verification is necessary to confirm the effectiveness of these vaccines in these models.</p></div>
eu_rights_str_mv openAccess
id Manara_b2078b3eee7558df7e1760bd2362df0d
identifier_str_mv 10.1371/journal.pone.0306559.t001
network_acronym_str Manara
network_name_str ManaraRepo
oai_identifier_str oai:figshare.com:article/27121440
publishDate 2024
repository.mail.fl_str_mv
repository.name.fl_str_mv
repository_id_str
rights_invalid_str_mv CC BY 4.0
spelling List of links used in this study.Ava Hashempour (11753878)Nastaran Khodadad (17535416)Peyman Bemani (10651254)Younes Ghasemi (3125685)Shokufeh Akbarinia (17535419)Reza Bordbari (19751532)Amir Hossein Tabatabaei (19751535)Shahab Falahi (18301765)MedicineMicrobiologyMolecular BiologyBiotechnologyImmunologyCancerInfectious DiseasesVirologyBiological Sciences not elsewhere classifiedmolecular dynamic stimulationimmunological simulation showeddiv >< pcodon optimization ensuredsimulate immune responsesstrong binding affinitieshuman vaccine model1 gag </strong bindinggag </1 </consistent responseshuman cellse </coli </γ inductionyet achievedworld ’vaccine modelsvaccine formulatedsuccessful translationsignificant progressreverse vaccinologyexperimental verificationepitopes locateddesigned constructsconserved domainschallenges facedbcl epitopesapproximately 93100 major<div><p>Significant progress has been made in <i>HIV-1</i> research; however, researchers have not yet achieved the objective of eradicating <i>HIV-1</i> infection. Accordingly, in this study, eucaryotic and procaryotic in silico vaccines were developed for <i>HIV-Gag</i> polyproteins from 100 major <i>HIV</i> subtypes and CRFs using immunoinformatic techniques to simulate immune responses in mice and humans. The epitopes located in the conserved domains of the <i>Gag</i> polyprotein were evaluated for allergenicity, antigenicity, immunogenicity, toxicity, homology, topology, and IFN-γ induction. Adjuvants, linkers, CTLs, HTLs, and BCL epitopes were incorporated into the vaccine models. Strong binding affinities were detected between HLA/MHC alleles, TLR-2, TLR-3, TLR-4, TLR-7, and TLR-9, and vaccine models. Immunological simulation showed that innate and adaptive immune cells elicited active and consistent responses. The human vaccine model was matched with approximately 93.91% of the human population. The strong binding of the vaccine to MHC/HLA and TLR molecules was confirmed through molecular dynamic stimulation. Codon optimization ensured the successful translation of the designed constructs into human cells and <i>E</i>. <i>coli</i> hosts. We believe that the <i>HIV-1 Gag</i> vaccine formulated in our research can reduce the challenges faced in developing an <i>HIV-1</i> vaccine. Nevertheless, experimental verification is necessary to confirm the effectiveness of these vaccines in these models.</p></div>2024-09-27T17:36:27ZDatasetinfo:eu-repo/semantics/publishedVersiondataset10.1371/journal.pone.0306559.t001https://figshare.com/articles/dataset/List_of_links_used_in_this_study_/27121440CC BY 4.0info:eu-repo/semantics/openAccessoai:figshare.com:article/271214402024-09-27T17:36:27Z
spellingShingle List of links used in this study.
Ava Hashempour (11753878)
Medicine
Microbiology
Molecular Biology
Biotechnology
Immunology
Cancer
Infectious Diseases
Virology
Biological Sciences not elsewhere classified
molecular dynamic stimulation
immunological simulation showed
div >< p
codon optimization ensured
simulate immune responses
strong binding affinities
human vaccine model
1 gag </
strong binding
gag </
1 </
consistent responses
human cells
e </
coli </
γ induction
yet achieved
world ’
vaccine models
vaccine formulated
successful translation
significant progress
reverse vaccinology
experimental verification
epitopes located
designed constructs
conserved domains
challenges faced
bcl epitopes
approximately 93
100 major
status_str publishedVersion
title List of links used in this study.
title_full List of links used in this study.
title_fullStr List of links used in this study.
title_full_unstemmed List of links used in this study.
title_short List of links used in this study.
title_sort List of links used in this study.
topic Medicine
Microbiology
Molecular Biology
Biotechnology
Immunology
Cancer
Infectious Diseases
Virology
Biological Sciences not elsewhere classified
molecular dynamic stimulation
immunological simulation showed
div >< p
codon optimization ensured
simulate immune responses
strong binding affinities
human vaccine model
1 gag </
strong binding
gag </
1 </
consistent responses
human cells
e </
coli </
γ induction
yet achieved
world ’
vaccine models
vaccine formulated
successful translation
significant progress
reverse vaccinology
experimental verification
epitopes located
designed constructs
conserved domains
challenges faced
bcl epitopes
approximately 93
100 major