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Harnessing Bioinformatic Approaches to Design Novel Multi-epitope Subunit Vaccine Against Leishmania infantum
Kala-azar or visceral leishmaniasis (VL) is the most important vector-borne protozoan disease and a life-threatening problem in the globe due to the lack of ideal vaccines or drugs. Recent advances in immunoinformatics and bioinformatics could be a promising approach in designing a new recombinant v...
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Published in: | International journal of peptide research and therapeutics 2020-09, Vol.26 (3), p.1417-1428 |
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container_title | International journal of peptide research and therapeutics |
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creator | Hashemzadeh, Pejman Ghorbanzadeh, Vajihe Lashgarian, Hamed Esmaeil Kheirandish, Farnaz Dariushnejad, Hassan |
description | Kala-azar or visceral leishmaniasis (VL) is the most important vector-borne protozoan disease and a life-threatening problem in the globe due to the lack of ideal vaccines or drugs. Recent advances in immunoinformatics and bioinformatics could be a promising approach in designing a new recombinant vaccine for VL treatment. In this study, a new recombinant vaccine against
Leishmania infantum
(
L. infantum
) designed by the computational method and Gp63, Hsp70 and Kmp11 antigens from
L. infantum
were selected as potential immunodominant epitopes. RpfE and RpfB from
Mycobacterium tuberculosis
used as adjuvants for enhancing vaccine immunogenicity. bioinformatic tools were used to analyze different aspects of the designed vaccine including, protein–protein interactions, B cell epitopes, MHC class I and II epitopes, the amino acid composition of multi-epitope vaccine, immunogenic behavior, and 3D homology modeling. This study revealed that our designed recombinant vaccine is able to induce responses of the immune system against
L. infantum
, and may be helpful to control VL infection, after appropriate in vitro and in vivo immunological assays. |
doi_str_mv | 10.1007/s10989-019-09949-6 |
format | article |
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Leishmania infantum
(
L. infantum
) designed by the computational method and Gp63, Hsp70 and Kmp11 antigens from
L. infantum
were selected as potential immunodominant epitopes. RpfE and RpfB from
Mycobacterium tuberculosis
used as adjuvants for enhancing vaccine immunogenicity. bioinformatic tools were used to analyze different aspects of the designed vaccine including, protein–protein interactions, B cell epitopes, MHC class I and II epitopes, the amino acid composition of multi-epitope vaccine, immunogenic behavior, and 3D homology modeling. This study revealed that our designed recombinant vaccine is able to induce responses of the immune system against
L. infantum
, and may be helpful to control VL infection, after appropriate in vitro and in vivo immunological assays.</description><identifier>ISSN: 1573-3149</identifier><identifier>EISSN: 1573-3904</identifier><identifier>DOI: 10.1007/s10989-019-09949-6</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Adjuvants ; Amino acid composition ; Animal Anatomy ; Antigens ; Biochemistry ; Bioinformatics ; Biomedical and Life Sciences ; Computer applications ; Epitopes ; Histology ; Homology ; Hsp70 protein ; Immune system ; Immunodominance ; Immunogenicity ; Immunosuppressive agents ; Leishmania infantum ; Life Sciences ; Major histocompatibility complex ; Molecular Medicine ; Morphology ; Pharmaceutical Sciences/Technology ; Pharmacology/Toxicology ; Polymer Sciences ; Protein interaction ; Protozoa ; Tuberculosis ; Vaccines ; Visceral leishmaniasis</subject><ispartof>International journal of peptide research and therapeutics, 2020-09, Vol.26 (3), p.1417-1428</ispartof><rights>Springer Nature B.V. 2019</rights><rights>Springer Nature B.V. 2019.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c319t-8fd59d4ab0c2d9a9b6bb24738088fc80874f0b8e46120f798c241a26a89ec98f3</citedby><cites>FETCH-LOGICAL-c319t-8fd59d4ab0c2d9a9b6bb24738088fc80874f0b8e46120f798c241a26a89ec98f3</cites><orcidid>0000-0003-2499-5631 ; 0000-0001-8039-9792 ; 0000-0002-4195-3516 ; 0000-0003-2680-0703 ; 0000-0003-2477-9461</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Hashemzadeh, Pejman</creatorcontrib><creatorcontrib>Ghorbanzadeh, Vajihe</creatorcontrib><creatorcontrib>Lashgarian, Hamed Esmaeil</creatorcontrib><creatorcontrib>Kheirandish, Farnaz</creatorcontrib><creatorcontrib>Dariushnejad, Hassan</creatorcontrib><title>Harnessing Bioinformatic Approaches to Design Novel Multi-epitope Subunit Vaccine Against Leishmania infantum</title><title>International journal of peptide research and therapeutics</title><addtitle>Int J Pept Res Ther</addtitle><description>Kala-azar or visceral leishmaniasis (VL) is the most important vector-borne protozoan disease and a life-threatening problem in the globe due to the lack of ideal vaccines or drugs. Recent advances in immunoinformatics and bioinformatics could be a promising approach in designing a new recombinant vaccine for VL treatment. In this study, a new recombinant vaccine against
Leishmania infantum
(
L. infantum
) designed by the computational method and Gp63, Hsp70 and Kmp11 antigens from
L. infantum
were selected as potential immunodominant epitopes. RpfE and RpfB from
Mycobacterium tuberculosis
used as adjuvants for enhancing vaccine immunogenicity. bioinformatic tools were used to analyze different aspects of the designed vaccine including, protein–protein interactions, B cell epitopes, MHC class I and II epitopes, the amino acid composition of multi-epitope vaccine, immunogenic behavior, and 3D homology modeling. This study revealed that our designed recombinant vaccine is able to induce responses of the immune system against
L. infantum
, and may be helpful to control VL infection, after appropriate in vitro and in vivo immunological assays.</description><subject>Adjuvants</subject><subject>Amino acid composition</subject><subject>Animal Anatomy</subject><subject>Antigens</subject><subject>Biochemistry</subject><subject>Bioinformatics</subject><subject>Biomedical and Life Sciences</subject><subject>Computer applications</subject><subject>Epitopes</subject><subject>Histology</subject><subject>Homology</subject><subject>Hsp70 protein</subject><subject>Immune system</subject><subject>Immunodominance</subject><subject>Immunogenicity</subject><subject>Immunosuppressive agents</subject><subject>Leishmania infantum</subject><subject>Life Sciences</subject><subject>Major histocompatibility complex</subject><subject>Molecular Medicine</subject><subject>Morphology</subject><subject>Pharmaceutical Sciences/Technology</subject><subject>Pharmacology/Toxicology</subject><subject>Polymer Sciences</subject><subject>Protein interaction</subject><subject>Protozoa</subject><subject>Tuberculosis</subject><subject>Vaccines</subject><subject>Visceral leishmaniasis</subject><issn>1573-3149</issn><issn>1573-3904</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9kEtPAyEUhYnRxFr9A65IXI8Cw8zAstZHTaoufGwJQ2FK04ERGBP_vWg17lzcx-Kcc3M_AE4xOscINRcRI854gXAuzikv6j0wwVVTFiVHdP93x5QfgqMYNwhVpMFoAvqFDE7HaF0HL623zvjQy2QVnA1D8FKtdYTJwysdbefgg3_XW3g_bpMt9GCTHzR8GtvR2QRfpVLWaTjrpHUxwaW2cd1LZyXMsdKlsT8GB0Zuoz75mVPwcnP9PF8Uy8fbu_lsWagS81Qws6r4isoWKbLikrd12xLalAwxZlTuDTWoZZrWmCDTcKYIxZLUknGtODPlFJztcvMLb6OOSWz8GFw-KQgljDBclSyryE6lgo8xaCOGYHsZPgRG4gur2GEVGav4xirqbCp3ppjFrtPhL_of1yeG7nxE</recordid><startdate>20200901</startdate><enddate>20200901</enddate><creator>Hashemzadeh, Pejman</creator><creator>Ghorbanzadeh, Vajihe</creator><creator>Lashgarian, Hamed Esmaeil</creator><creator>Kheirandish, Farnaz</creator><creator>Dariushnejad, Hassan</creator><general>Springer Netherlands</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88I</scope><scope>8AO</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M2P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><orcidid>https://orcid.org/0000-0003-2499-5631</orcidid><orcidid>https://orcid.org/0000-0001-8039-9792</orcidid><orcidid>https://orcid.org/0000-0002-4195-3516</orcidid><orcidid>https://orcid.org/0000-0003-2680-0703</orcidid><orcidid>https://orcid.org/0000-0003-2477-9461</orcidid></search><sort><creationdate>20200901</creationdate><title>Harnessing Bioinformatic Approaches to Design Novel Multi-epitope Subunit Vaccine Against Leishmania infantum</title><author>Hashemzadeh, Pejman ; Ghorbanzadeh, Vajihe ; Lashgarian, Hamed Esmaeil ; Kheirandish, Farnaz ; Dariushnejad, Hassan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c319t-8fd59d4ab0c2d9a9b6bb24738088fc80874f0b8e46120f798c241a26a89ec98f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Adjuvants</topic><topic>Amino acid composition</topic><topic>Animal Anatomy</topic><topic>Antigens</topic><topic>Biochemistry</topic><topic>Bioinformatics</topic><topic>Biomedical and Life Sciences</topic><topic>Computer applications</topic><topic>Epitopes</topic><topic>Histology</topic><topic>Homology</topic><topic>Hsp70 protein</topic><topic>Immune system</topic><topic>Immunodominance</topic><topic>Immunogenicity</topic><topic>Immunosuppressive agents</topic><topic>Leishmania infantum</topic><topic>Life Sciences</topic><topic>Major histocompatibility complex</topic><topic>Molecular Medicine</topic><topic>Morphology</topic><topic>Pharmaceutical Sciences/Technology</topic><topic>Pharmacology/Toxicology</topic><topic>Polymer Sciences</topic><topic>Protein interaction</topic><topic>Protozoa</topic><topic>Tuberculosis</topic><topic>Vaccines</topic><topic>Visceral leishmaniasis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hashemzadeh, Pejman</creatorcontrib><creatorcontrib>Ghorbanzadeh, Vajihe</creatorcontrib><creatorcontrib>Lashgarian, Hamed Esmaeil</creatorcontrib><creatorcontrib>Kheirandish, Farnaz</creatorcontrib><creatorcontrib>Dariushnejad, Hassan</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><jtitle>International journal of peptide research and therapeutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hashemzadeh, Pejman</au><au>Ghorbanzadeh, Vajihe</au><au>Lashgarian, Hamed Esmaeil</au><au>Kheirandish, Farnaz</au><au>Dariushnejad, Hassan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Harnessing Bioinformatic Approaches to Design Novel Multi-epitope Subunit Vaccine Against Leishmania infantum</atitle><jtitle>International journal of peptide research and therapeutics</jtitle><stitle>Int J Pept Res Ther</stitle><date>2020-09-01</date><risdate>2020</risdate><volume>26</volume><issue>3</issue><spage>1417</spage><epage>1428</epage><pages>1417-1428</pages><issn>1573-3149</issn><eissn>1573-3904</eissn><abstract>Kala-azar or visceral leishmaniasis (VL) is the most important vector-borne protozoan disease and a life-threatening problem in the globe due to the lack of ideal vaccines or drugs. Recent advances in immunoinformatics and bioinformatics could be a promising approach in designing a new recombinant vaccine for VL treatment. In this study, a new recombinant vaccine against
Leishmania infantum
(
L. infantum
) designed by the computational method and Gp63, Hsp70 and Kmp11 antigens from
L. infantum
were selected as potential immunodominant epitopes. RpfE and RpfB from
Mycobacterium tuberculosis
used as adjuvants for enhancing vaccine immunogenicity. bioinformatic tools were used to analyze different aspects of the designed vaccine including, protein–protein interactions, B cell epitopes, MHC class I and II epitopes, the amino acid composition of multi-epitope vaccine, immunogenic behavior, and 3D homology modeling. This study revealed that our designed recombinant vaccine is able to induce responses of the immune system against
L. infantum
, and may be helpful to control VL infection, after appropriate in vitro and in vivo immunological assays.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><doi>10.1007/s10989-019-09949-6</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0003-2499-5631</orcidid><orcidid>https://orcid.org/0000-0001-8039-9792</orcidid><orcidid>https://orcid.org/0000-0002-4195-3516</orcidid><orcidid>https://orcid.org/0000-0003-2680-0703</orcidid><orcidid>https://orcid.org/0000-0003-2477-9461</orcidid></addata></record> |
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subjects | Adjuvants Amino acid composition Animal Anatomy Antigens Biochemistry Bioinformatics Biomedical and Life Sciences Computer applications Epitopes Histology Homology Hsp70 protein Immune system Immunodominance Immunogenicity Immunosuppressive agents Leishmania infantum Life Sciences Major histocompatibility complex Molecular Medicine Morphology Pharmaceutical Sciences/Technology Pharmacology/Toxicology Polymer Sciences Protein interaction Protozoa Tuberculosis Vaccines Visceral leishmaniasis |
title | Harnessing Bioinformatic Approaches to Design Novel Multi-epitope Subunit Vaccine Against Leishmania infantum |
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