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Enhanced Vaccine-Induced CD8(+) T Cell Responses to Malaria Antigen ME-TRAP by Fusion to MHC Class II Invariant Chain

The orthodox role of the invariant chain (CD74; Ii) is in antigen presentation to CD4(+) T cells, but enhanced CD8(+) T cells responses have been reported after vaccination with vectored viral vaccines encoding a fusion of Ii to the antigen of interest. In this study we assessed whether fusion of th...

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Autores principales: Spencer, Alexandra J., Cottingham, Matthew G., Jenks, Jennifer A., Longley, Rhea J., Capone, Stefania, Colloca, Stefano, Folgori, Antonella, Cortese, Riccardo, Nicosia, Alfredo, Bregu, Migena, Hill, Adrian V. S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4063960/
https://www.ncbi.nlm.nih.gov/pubmed/24945248
http://dx.doi.org/10.1371/journal.pone.0100538
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author Spencer, Alexandra J.
Cottingham, Matthew G.
Jenks, Jennifer A.
Longley, Rhea J.
Capone, Stefania
Colloca, Stefano
Folgori, Antonella
Cortese, Riccardo
Nicosia, Alfredo
Bregu, Migena
Hill, Adrian V. S.
author_facet Spencer, Alexandra J.
Cottingham, Matthew G.
Jenks, Jennifer A.
Longley, Rhea J.
Capone, Stefania
Colloca, Stefano
Folgori, Antonella
Cortese, Riccardo
Nicosia, Alfredo
Bregu, Migena
Hill, Adrian V. S.
author_sort Spencer, Alexandra J.
collection PubMed
description The orthodox role of the invariant chain (CD74; Ii) is in antigen presentation to CD4(+) T cells, but enhanced CD8(+) T cells responses have been reported after vaccination with vectored viral vaccines encoding a fusion of Ii to the antigen of interest. In this study we assessed whether fusion of the malarial antigen, ME-TRAP, to Ii could increase the vaccine-induced CD8(+) T cell response. Following single or heterologous prime-boost vaccination of mice with a recombinant chimpanzee adenovirus vector, ChAd63, or recombinant modified vaccinia virus Ankara (MVA), higher frequencies of antigen-specific CD4(+) and CD8(+) T cells were observed, with the largest increases observed following a ChAd63-MVA heterologous prime-boost regimen. Studies in non-human primates confirmed the ability of Ii-fusion to augment the T cell response, where a 4-fold increase was maintained up to 11 weeks after the MVA boost. Of the numerous different approaches explored to increase vectored vaccine induced immunogenicity over the years, fusion to the invariant chain showed a consistent enhancement in CD8(+) T cell responses across different animal species and may therefore find application in the development of vaccines against human malaria and other diseases where high levels of cell-mediated immunity are required.
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spelling pubmed-40639602014-06-25 Enhanced Vaccine-Induced CD8(+) T Cell Responses to Malaria Antigen ME-TRAP by Fusion to MHC Class II Invariant Chain Spencer, Alexandra J. Cottingham, Matthew G. Jenks, Jennifer A. Longley, Rhea J. Capone, Stefania Colloca, Stefano Folgori, Antonella Cortese, Riccardo Nicosia, Alfredo Bregu, Migena Hill, Adrian V. S. PLoS One Research Article The orthodox role of the invariant chain (CD74; Ii) is in antigen presentation to CD4(+) T cells, but enhanced CD8(+) T cells responses have been reported after vaccination with vectored viral vaccines encoding a fusion of Ii to the antigen of interest. In this study we assessed whether fusion of the malarial antigen, ME-TRAP, to Ii could increase the vaccine-induced CD8(+) T cell response. Following single or heterologous prime-boost vaccination of mice with a recombinant chimpanzee adenovirus vector, ChAd63, or recombinant modified vaccinia virus Ankara (MVA), higher frequencies of antigen-specific CD4(+) and CD8(+) T cells were observed, with the largest increases observed following a ChAd63-MVA heterologous prime-boost regimen. Studies in non-human primates confirmed the ability of Ii-fusion to augment the T cell response, where a 4-fold increase was maintained up to 11 weeks after the MVA boost. Of the numerous different approaches explored to increase vectored vaccine induced immunogenicity over the years, fusion to the invariant chain showed a consistent enhancement in CD8(+) T cell responses across different animal species and may therefore find application in the development of vaccines against human malaria and other diseases where high levels of cell-mediated immunity are required. Public Library of Science 2014-06-19 /pmc/articles/PMC4063960/ /pubmed/24945248 http://dx.doi.org/10.1371/journal.pone.0100538 Text en © 2014 Spencer et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Spencer, Alexandra J.
Cottingham, Matthew G.
Jenks, Jennifer A.
Longley, Rhea J.
Capone, Stefania
Colloca, Stefano
Folgori, Antonella
Cortese, Riccardo
Nicosia, Alfredo
Bregu, Migena
Hill, Adrian V. S.
Enhanced Vaccine-Induced CD8(+) T Cell Responses to Malaria Antigen ME-TRAP by Fusion to MHC Class II Invariant Chain
title Enhanced Vaccine-Induced CD8(+) T Cell Responses to Malaria Antigen ME-TRAP by Fusion to MHC Class II Invariant Chain
title_full Enhanced Vaccine-Induced CD8(+) T Cell Responses to Malaria Antigen ME-TRAP by Fusion to MHC Class II Invariant Chain
title_fullStr Enhanced Vaccine-Induced CD8(+) T Cell Responses to Malaria Antigen ME-TRAP by Fusion to MHC Class II Invariant Chain
title_full_unstemmed Enhanced Vaccine-Induced CD8(+) T Cell Responses to Malaria Antigen ME-TRAP by Fusion to MHC Class II Invariant Chain
title_short Enhanced Vaccine-Induced CD8(+) T Cell Responses to Malaria Antigen ME-TRAP by Fusion to MHC Class II Invariant Chain
title_sort enhanced vaccine-induced cd8(+) t cell responses to malaria antigen me-trap by fusion to mhc class ii invariant chain
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4063960/
https://www.ncbi.nlm.nih.gov/pubmed/24945248
http://dx.doi.org/10.1371/journal.pone.0100538
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