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DNA vaccines: prime time is now
Recently newer synthetic DNA vaccines have been rapidly advanced to clinical study and have demonstrated an impressive degree of immune potency and tolerability. Improvements in DNA delivery over prior needle and syringe approaches include jet delivery, gene gun delivery, among others. Among the mos...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7195337/ https://www.ncbi.nlm.nih.gov/pubmed/32259744 http://dx.doi.org/10.1016/j.coi.2020.01.006 |
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author | Gary, Ebony N Weiner, David B |
author_facet | Gary, Ebony N Weiner, David B |
author_sort | Gary, Ebony N |
collection | PubMed |
description | Recently newer synthetic DNA vaccines have been rapidly advanced to clinical study and have demonstrated an impressive degree of immune potency and tolerability. Improvements in DNA delivery over prior needle and syringe approaches include jet delivery, gene gun delivery, among others. Among the most effective of these new delivery methods, advanced electroporation (EP), combined with other advances, induces robust humoral and cellular immunity in both preventative as well as therapeutic studies. Advancements in the design of the DNA inserts include leader sequence changes, RNA and codon optimizations, improved insert designs, increased concentrations of DNA, and skin delivery, appear to complement newer delivery strategies. These advances also provide a framework for the in vivo production of synthetic DNA biologics. In this review, we focus on recent studies of synthetic DNA vaccines in the clinic for the prevention or treatment of infectious diseases with a focus on adaptive electroporation for delivery, and briefly summarize novel preclinical data advancing the in vivo delivery of DNA-encoded antibody-like biologics. |
format | Online Article Text |
id | pubmed-7195337 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-71953372020-05-02 DNA vaccines: prime time is now Gary, Ebony N Weiner, David B Curr Opin Immunol Article Recently newer synthetic DNA vaccines have been rapidly advanced to clinical study and have demonstrated an impressive degree of immune potency and tolerability. Improvements in DNA delivery over prior needle and syringe approaches include jet delivery, gene gun delivery, among others. Among the most effective of these new delivery methods, advanced electroporation (EP), combined with other advances, induces robust humoral and cellular immunity in both preventative as well as therapeutic studies. Advancements in the design of the DNA inserts include leader sequence changes, RNA and codon optimizations, improved insert designs, increased concentrations of DNA, and skin delivery, appear to complement newer delivery strategies. These advances also provide a framework for the in vivo production of synthetic DNA biologics. In this review, we focus on recent studies of synthetic DNA vaccines in the clinic for the prevention or treatment of infectious diseases with a focus on adaptive electroporation for delivery, and briefly summarize novel preclinical data advancing the in vivo delivery of DNA-encoded antibody-like biologics. Elsevier 2020-08 /pmc/articles/PMC7195337/ /pubmed/32259744 http://dx.doi.org/10.1016/j.coi.2020.01.006 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Gary, Ebony N Weiner, David B DNA vaccines: prime time is now |
title | DNA vaccines: prime time is now |
title_full | DNA vaccines: prime time is now |
title_fullStr | DNA vaccines: prime time is now |
title_full_unstemmed | DNA vaccines: prime time is now |
title_short | DNA vaccines: prime time is now |
title_sort | dna vaccines: prime time is now |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7195337/ https://www.ncbi.nlm.nih.gov/pubmed/32259744 http://dx.doi.org/10.1016/j.coi.2020.01.006 |
work_keys_str_mv | AT garyebonyn dnavaccinesprimetimeisnow AT weinerdavidb dnavaccinesprimetimeisnow |