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About:
In silico CD4+, CD8+ T-cell and B-cell immunity associated immunogenic epitope prediction and HLA distribution analysis of Zika virus
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wasabi.inria.fr
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Type:
Academic Article
research paper
schema:ScholarlyArticle
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
title
In silico CD4+, CD8+ T-cell and B-cell immunity associated immunogenic epitope prediction and HLA distribution analysis of Zika virus
Creator
Dhasmana, Anupam
Haque, Shafiul
Lohani, Mohtashim
Raza, Sana
Srivastava, Vandana
Areeshi, Mohammed
Arif, Jamal
Janahi, Essam
Sarangi, Aditya
Saxena, Anand
Bhatt, Bramha
Essam, Mohammed
Janahi,
Lal, Madan
source
PMC
abstract
Zika virus (ZIKV) is a mosquito-borne flavivirus distributed all over Africa, South America and Asia. The infection with the virus may cause acute febrile sickness that clinically resembles dengue fever, yet there is no vaccine, no satisfactory treatment, and no means of evaluating the risk of the disease or prognosis in the infected people. In the present study, the efficacy of the host's immune response in reducing the risk of infectious diseases was taken into account to carry out immuno-informatics driven epitope screening strategy of vaccine candidates against ZIKV. In this study, HLA distribution analysis was done to ensure the coverage of the vast majority of the population. Systematic screening of effective dominant immunogens was done with the help of Immune Epitope & ABCPred databases. The outcomes suggested that the predicted epitopes may be protective immunogens with highly conserved sequences and bear potential to induce both protective neutralizing antibodies, T & B cell responses. A total of 25 CD4+ and 16 CD8+ peptides were screened for T-cell mediated immunity. The predicted epitope %22TGLDFSDLYYLTMNNKHWLV%22 was selected as a highly immunogenic epitope for humoral immunity. These peptides were further screened as non-toxic, immunogenic and non-mutated residues of envelop viral protein. The predicted epitope could work as suitable candidate(s) for peptide based vaccine development. Further, experimental validation of these epitopes is warranted to ensure the potential of B- and T-cells stimulation for their efficient use as vaccine candidates, and as diagnostic agents against ZIKV.
has issue date
2017-01-13
(
xsd:dateTime
)
bibo:doi
10.17179/excli2016-719
bibo:pmid
28435428
has license
cc-by
sha1sum (hex)
57bac09c0563474a03a233b1e7f60ed8c82a9642
schema:url
https://doi.org/10.17179/excli2016-719
resource representing a document's title
In silico CD4+, CD8+ T-cell and B-cell immunity associated immunogenic epitope prediction and HLA distribution analysis of Zika virus
has PubMed Central identifier
PMC5379118
has PubMed identifier
28435428
schema:publication
EXCLI J
resource representing a document's body
covid:57bac09c0563474a03a233b1e7f60ed8c82a9642#body_text
is
schema:about
of
named entity 'ANALYSIS'
named entity 'IMMUNOGENIC'
named entity 'HLA'
named entity 'EPITOPE PREDICTION'
named entity 'HLA'
named entity 'B-CELL'
named entity 'IMMUNITY'
named entity 'IN SILICO'
named entity 'ASSOCIATED'
named entity 'DISTRIBUTION'
named entity 'T-CELL'
named entity 'ZIKA VIRUS'
named entity 'CD4'
named entity 'CD8'
named entity 'ZIKA VIRUS'
named entity 'T-CELL'
named entity 'protein'
named entity 'immunogenic'
named entity 'epitope'
named entity 'Zika forest'
named entity 'Flaviviridae'
named entity 'HLA'
named entity 'MHC-I'
named entity 'epitopic'
named entity 'vaccine'
named entity 'antigenicity'
named entity 'epitopes'
named entity 'antigens'
named entity 'H1N1'
named entity 'epitopes'
named entity 'vaccine'
named entity 'deionized water'
named entity 'T-cell activation'
named entity 'epitopes'
named entity 'peptides'
named entity 'immunogenic'
named entity 'viral envelope protein'
named entity 'open reading frame'
named entity 'immunogenicity'
named entity 'HLA'
named entity 'HLA'
named entity 'epitope'
named entity 'isopropanol'
named entity 'acetic acid'
named entity 'virus'
named entity 'conserved regions'
named entity 'vaccine'
named entity 'CD4+'
named entity 'virus'
named entity 'epitopes'
named entity 'worldwide distribution'
named entity 'epitope'
named entity 'antigen'
named entity 'Zika'
named entity 'CD4+ T-cells'
named entity 'virus'
named entity 'epitopes'
named entity 'SVM'
named entity 'epitopes'
named entity 'Zika fever'
named entity 'helper T-cell'
named entity 'MHC'
named entity 'epitopes'
named entity 'epitope'
named entity 'HLA'
named entity 'HLA'
named entity 'virus'
named entity 'peptide'
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