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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2014
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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. |
format | Online Article Text |
id | pubmed-4494222 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT uratakehiro developmentsinviralvectorbasedvaccines AT okudakenji developmentsinviralvectorbasedvaccines AT shimadamasaru developmentsinviralvectorbasedvaccines |