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Developments in Viral Vector-Based Vaccines

Viral vectors are promising tools for gene therapy and vaccines. Viral vector-based vaccines can enhance immunogenicity without an adjuvant and induce a robust cytotoxic T lymphocyte (CTL) response to eliminate virus-infected cells. During the last several decades, many types of viruses have been de...

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Detalles Bibliográficos
Autores principales: Ura, Takehiro, Okuda, Kenji, Shimada, Masaru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4494222/
https://www.ncbi.nlm.nih.gov/pubmed/26344749
http://dx.doi.org/10.3390/vaccines2030624
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author Ura, Takehiro
Okuda, Kenji
Shimada, Masaru
author_facet Ura, Takehiro
Okuda, Kenji
Shimada, Masaru
author_sort Ura, Takehiro
collection PubMed
description Viral vectors are promising tools for gene therapy and vaccines. Viral vector-based vaccines can enhance immunogenicity without an adjuvant and induce a robust cytotoxic T lymphocyte (CTL) response to eliminate virus-infected cells. During the last several decades, many types of viruses have been developed as vaccine vectors. Each has unique features and parental virus-related risks. In addition, genetically altered vectors have been developed to improve efficacy and safety, reduce administration dose, and enable large-scale manufacturing. To date, both successful and unsuccessful results have been reported in clinical trials. These trials provide important information on factors such as toxicity, administration dose tolerated, and optimized vaccination strategy. This review highlights major viral vectors that are the best candidates for clinical use.
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spelling pubmed-44942222015-08-31 Developments in Viral Vector-Based Vaccines Ura, Takehiro Okuda, Kenji Shimada, Masaru Vaccines (Basel) Review Viral vectors are promising tools for gene therapy and vaccines. Viral vector-based vaccines can enhance immunogenicity without an adjuvant and induce a robust cytotoxic T lymphocyte (CTL) response to eliminate virus-infected cells. During the last several decades, many types of viruses have been developed as vaccine vectors. Each has unique features and parental virus-related risks. In addition, genetically altered vectors have been developed to improve efficacy and safety, reduce administration dose, and enable large-scale manufacturing. To date, both successful and unsuccessful results have been reported in clinical trials. These trials provide important information on factors such as toxicity, administration dose tolerated, and optimized vaccination strategy. This review highlights major viral vectors that are the best candidates for clinical use. MDPI 2014-07-29 /pmc/articles/PMC4494222/ /pubmed/26344749 http://dx.doi.org/10.3390/vaccines2030624 Text en © 2014 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Ura, Takehiro
Okuda, Kenji
Shimada, Masaru
Developments in Viral Vector-Based Vaccines
title Developments in Viral Vector-Based Vaccines
title_full Developments in Viral Vector-Based Vaccines
title_fullStr Developments in Viral Vector-Based Vaccines
title_full_unstemmed Developments in Viral Vector-Based Vaccines
title_short Developments in Viral Vector-Based Vaccines
title_sort developments in viral vector-based vaccines
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4494222/
https://www.ncbi.nlm.nih.gov/pubmed/26344749
http://dx.doi.org/10.3390/vaccines2030624
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