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Plasmid DNA-Based Alphavirus Vaccines

Alphaviruses have been engineered as vectors for high-level transgene expression. Originally, alphavirus-based vectors were applied as recombinant replication-deficient particles, subjected to expression studies in mammalian and non-mammalian cell lines, primary cell cultures, and in vivo. However,...

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Detalles Bibliográficos
Autor principal: Lundstrom, Kenneth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6466081/
https://www.ncbi.nlm.nih.gov/pubmed/30857255
http://dx.doi.org/10.3390/vaccines7010029
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author Lundstrom, Kenneth
author_facet Lundstrom, Kenneth
author_sort Lundstrom, Kenneth
collection PubMed
description Alphaviruses have been engineered as vectors for high-level transgene expression. Originally, alphavirus-based vectors were applied as recombinant replication-deficient particles, subjected to expression studies in mammalian and non-mammalian cell lines, primary cell cultures, and in vivo. However, vector engineering has expanded the application range to plasmid DNA-based delivery and expression. Immunization studies with DNA-based alphavirus vectors have demonstrated tumor regression and protection against challenges with infectious agents and tumor cells in animal tumor models. The presence of the RNA replicon genes responsible for extensive RNA replication in the RNA/DNA layered alphavirus vectors provides superior transgene expression in comparison to conventional plasmid DNA-based expression. Immunization with alphavirus DNA vectors revealed that 1000-fold less DNA was required to elicit similar immune responses compared to conventional plasmid DNA. In addition to DNA-based delivery, immunization with recombinant alphavirus particles and RNA replicons has demonstrated efficacy in providing protection against lethal challenges by infectious agents and tumor cells.
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spelling pubmed-64660812019-04-18 Plasmid DNA-Based Alphavirus Vaccines Lundstrom, Kenneth Vaccines (Basel) Review Alphaviruses have been engineered as vectors for high-level transgene expression. Originally, alphavirus-based vectors were applied as recombinant replication-deficient particles, subjected to expression studies in mammalian and non-mammalian cell lines, primary cell cultures, and in vivo. However, vector engineering has expanded the application range to plasmid DNA-based delivery and expression. Immunization studies with DNA-based alphavirus vectors have demonstrated tumor regression and protection against challenges with infectious agents and tumor cells in animal tumor models. The presence of the RNA replicon genes responsible for extensive RNA replication in the RNA/DNA layered alphavirus vectors provides superior transgene expression in comparison to conventional plasmid DNA-based expression. Immunization with alphavirus DNA vectors revealed that 1000-fold less DNA was required to elicit similar immune responses compared to conventional plasmid DNA. In addition to DNA-based delivery, immunization with recombinant alphavirus particles and RNA replicons has demonstrated efficacy in providing protection against lethal challenges by infectious agents and tumor cells. MDPI 2019-03-08 /pmc/articles/PMC6466081/ /pubmed/30857255 http://dx.doi.org/10.3390/vaccines7010029 Text en © 2019 by the author. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Lundstrom, Kenneth
Plasmid DNA-Based Alphavirus Vaccines
title Plasmid DNA-Based Alphavirus Vaccines
title_full Plasmid DNA-Based Alphavirus Vaccines
title_fullStr Plasmid DNA-Based Alphavirus Vaccines
title_full_unstemmed Plasmid DNA-Based Alphavirus Vaccines
title_short Plasmid DNA-Based Alphavirus Vaccines
title_sort plasmid dna-based alphavirus vaccines
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6466081/
https://www.ncbi.nlm.nih.gov/pubmed/30857255
http://dx.doi.org/10.3390/vaccines7010029
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