Exploring Leishmania secretory proteins to design B and T cell multi-epitope subunit vaccine using immunoinformatics approach

Abstract Visceral leishmaniasis (VL) is a fatal form of leishmaniasis which affects 70 countries, worldwide. Increasing drug resistance, HIV co-infection, and poor health system require operative vaccination strategy to control the VL transmission dynamics. Therefore, a holistic approach is needed t...

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Autores principales: Nazia Khatoon, Rajan Kumar Pandey, Vijay Kumar Prajapati
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Publicado: Nature Portfolio 2017
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Acceso en línea:https://doaj.org/article/aa69508035654814bc26da9f7d57da83
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spelling oai:doaj.org-article:aa69508035654814bc26da9f7d57da832021-12-02T12:32:50ZExploring Leishmania secretory proteins to design B and T cell multi-epitope subunit vaccine using immunoinformatics approach10.1038/s41598-017-08842-w2045-2322https://doaj.org/article/aa69508035654814bc26da9f7d57da832017-08-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-08842-whttps://doaj.org/toc/2045-2322Abstract Visceral leishmaniasis (VL) is a fatal form of leishmaniasis which affects 70 countries, worldwide. Increasing drug resistance, HIV co-infection, and poor health system require operative vaccination strategy to control the VL transmission dynamics. Therefore, a holistic approach is needed to generate T and B memory cells to mediate long-term immunity against VL infection. Consequently, immunoinformatics approach was applied to design Leishmania secretory protein based multi-epitope subunit vaccine construct consisting of B and T cell epitopes. Further, the physiochemical characterization was performed to check the aliphatic index, theoretical PI, molecular weight, and thermostable nature of vaccine construct. The allergenicity and antigenicity were also predicted to ensure the safety and immunogenic behavior of final vaccine construct. Moreover, homology modeling, followed by molecular docking and molecular dynamics simulation study was also performed to evaluate the binding affinity and stability of receptor (TLR-4) and ligand (vaccine protein) complex. This study warrants the experimental validation to ensure the immunogenicity and safety profile of presented vaccine construct which may be further helpful to control VL infection.Nazia KhatoonRajan Kumar PandeyVijay Kumar PrajapatiNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-12 (2017)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Nazia Khatoon
Rajan Kumar Pandey
Vijay Kumar Prajapati
Exploring Leishmania secretory proteins to design B and T cell multi-epitope subunit vaccine using immunoinformatics approach
description Abstract Visceral leishmaniasis (VL) is a fatal form of leishmaniasis which affects 70 countries, worldwide. Increasing drug resistance, HIV co-infection, and poor health system require operative vaccination strategy to control the VL transmission dynamics. Therefore, a holistic approach is needed to generate T and B memory cells to mediate long-term immunity against VL infection. Consequently, immunoinformatics approach was applied to design Leishmania secretory protein based multi-epitope subunit vaccine construct consisting of B and T cell epitopes. Further, the physiochemical characterization was performed to check the aliphatic index, theoretical PI, molecular weight, and thermostable nature of vaccine construct. The allergenicity and antigenicity were also predicted to ensure the safety and immunogenic behavior of final vaccine construct. Moreover, homology modeling, followed by molecular docking and molecular dynamics simulation study was also performed to evaluate the binding affinity and stability of receptor (TLR-4) and ligand (vaccine protein) complex. This study warrants the experimental validation to ensure the immunogenicity and safety profile of presented vaccine construct which may be further helpful to control VL infection.
format article
author Nazia Khatoon
Rajan Kumar Pandey
Vijay Kumar Prajapati
author_facet Nazia Khatoon
Rajan Kumar Pandey
Vijay Kumar Prajapati
author_sort Nazia Khatoon
title Exploring Leishmania secretory proteins to design B and T cell multi-epitope subunit vaccine using immunoinformatics approach
title_short Exploring Leishmania secretory proteins to design B and T cell multi-epitope subunit vaccine using immunoinformatics approach
title_full Exploring Leishmania secretory proteins to design B and T cell multi-epitope subunit vaccine using immunoinformatics approach
title_fullStr Exploring Leishmania secretory proteins to design B and T cell multi-epitope subunit vaccine using immunoinformatics approach
title_full_unstemmed Exploring Leishmania secretory proteins to design B and T cell multi-epitope subunit vaccine using immunoinformatics approach
title_sort exploring leishmania secretory proteins to design b and t cell multi-epitope subunit vaccine using immunoinformatics approach
publisher Nature Portfolio
publishDate 2017
url https://doaj.org/article/aa69508035654814bc26da9f7d57da83
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AT rajankumarpandey exploringleishmaniasecretoryproteinstodesignbandtcellmultiepitopesubunitvaccineusingimmunoinformaticsapproach
AT vijaykumarprajapati exploringleishmaniasecretoryproteinstodesignbandtcellmultiepitopesubunitvaccineusingimmunoinformaticsapproach
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