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DNA Vaccines for Biodefense and Emerging and Neglected Infectious Diseases

Abstract Continued improvements in vaccination technologies have led to remarkable progress in the control of human infectious diseases. Our fundamental view of the nature of a vaccine was changed with the discovery of DNA immunization in the early 1990s when it was determined that the genetic mater...

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Autores principales: Lu, Shan, Grimes-Serrano, Jill M., Wang, Shixia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7150048/
http://dx.doi.org/10.1016/B978-0-12-369408-9.00008-1
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author Lu, Shan
Grimes-Serrano, Jill M.
Wang, Shixia
author_facet Lu, Shan
Grimes-Serrano, Jill M.
Wang, Shixia
author_sort Lu, Shan
collection PubMed
description Abstract Continued improvements in vaccination technologies have led to remarkable progress in the control of human infectious diseases. Our fundamental view of the nature of a vaccine was changed with the discovery of DNA immunization in the early 1990s when it was determined that the genetic material that encodes for antigens, rather than the actual antigens themselves, can be effective in eliciting an immune response. Given the ever increasing threat of emerging and reemerging infectious diseases and a renewed concern regarding the use of biological agents for bioterrorism purposes, the opportunities that DNA vaccine technology provides could not have come at a more critical time in history. Since its inception, DNA vaccination technology has undergone significant advancements and many candidate human vaccine formulations have already been developed. Improved modes of administration, the use of codon and antigen gene optimization, and the implementation of vaccination DNA prime/boost regimens have led to the quick progression of DNA vaccines from research laboratory benches to human clinical trials. Significant progress has been made in developing DNA vaccines against various biodefense and emerging infectious disease targets, such as HIV-1, influenza, severe acute respiratory syndrome associated coronavirus (SARS-CoV), Ebola, the viral encephalitides, anthrax, plague, and botulism, among others with some already moving into early phase clinical trials with promising results. Having the ability to respond to a potential bioterrorism threat or to some other emerging infectious disease outbreak is crucial and the advancements associated with DNA vaccination technology will allow us to do so in a prompt and rational matter.
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spelling pubmed-71500482020-04-13 DNA Vaccines for Biodefense and Emerging and Neglected Infectious Diseases Lu, Shan Grimes-Serrano, Jill M. Wang, Shixia Vaccines for Biodefense and Emerging and Neglected Diseases Article Abstract Continued improvements in vaccination technologies have led to remarkable progress in the control of human infectious diseases. Our fundamental view of the nature of a vaccine was changed with the discovery of DNA immunization in the early 1990s when it was determined that the genetic material that encodes for antigens, rather than the actual antigens themselves, can be effective in eliciting an immune response. Given the ever increasing threat of emerging and reemerging infectious diseases and a renewed concern regarding the use of biological agents for bioterrorism purposes, the opportunities that DNA vaccine technology provides could not have come at a more critical time in history. Since its inception, DNA vaccination technology has undergone significant advancements and many candidate human vaccine formulations have already been developed. Improved modes of administration, the use of codon and antigen gene optimization, and the implementation of vaccination DNA prime/boost regimens have led to the quick progression of DNA vaccines from research laboratory benches to human clinical trials. Significant progress has been made in developing DNA vaccines against various biodefense and emerging infectious disease targets, such as HIV-1, influenza, severe acute respiratory syndrome associated coronavirus (SARS-CoV), Ebola, the viral encephalitides, anthrax, plague, and botulism, among others with some already moving into early phase clinical trials with promising results. Having the ability to respond to a potential bioterrorism threat or to some other emerging infectious disease outbreak is crucial and the advancements associated with DNA vaccination technology will allow us to do so in a prompt and rational matter. 2009 2009-01-30 /pmc/articles/PMC7150048/ http://dx.doi.org/10.1016/B978-0-12-369408-9.00008-1 Text en Copyright © 2009 Elsevier Inc. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Lu, Shan
Grimes-Serrano, Jill M.
Wang, Shixia
DNA Vaccines for Biodefense and Emerging and Neglected Infectious Diseases
title DNA Vaccines for Biodefense and Emerging and Neglected Infectious Diseases
title_full DNA Vaccines for Biodefense and Emerging and Neglected Infectious Diseases
title_fullStr DNA Vaccines for Biodefense and Emerging and Neglected Infectious Diseases
title_full_unstemmed DNA Vaccines for Biodefense and Emerging and Neglected Infectious Diseases
title_short DNA Vaccines for Biodefense and Emerging and Neglected Infectious Diseases
title_sort dna vaccines for biodefense and emerging and neglected infectious diseases
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7150048/
http://dx.doi.org/10.1016/B978-0-12-369408-9.00008-1
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