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A Review on Dengue Vaccine Development
Dengue virus (DENV) has become a global health threat with about half of the world’s population at risk of infection. Although the disease caused by DENV is self-limiting in the first infection, the antibody-dependent enhancement (ADE) effect increases the mortality in the second infection with a he...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7159032/ https://www.ncbi.nlm.nih.gov/pubmed/32024238 http://dx.doi.org/10.3390/vaccines8010063 |
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author | Deng, Sheng-Qun Yang, Xian Wei, Yong Chen, Jia-Ting Wang, Xiao-Jun Peng, Hong-Juan |
author_facet | Deng, Sheng-Qun Yang, Xian Wei, Yong Chen, Jia-Ting Wang, Xiao-Jun Peng, Hong-Juan |
author_sort | Deng, Sheng-Qun |
collection | PubMed |
description | Dengue virus (DENV) has become a global health threat with about half of the world’s population at risk of infection. Although the disease caused by DENV is self-limiting in the first infection, the antibody-dependent enhancement (ADE) effect increases the mortality in the second infection with a heterotypic virus. Since there is no specific efficient medicine in treatment, it is urgent to develop vaccines to prevent infection and disease progression. Currently, only a live attenuated vaccine, chimeric yellow fever 17D—tetravalent dengue vaccine (CYD-TDV), has been licensed for clinical use in some countries, and many candidate vaccines are still under research and development. This review discusses the progress, strengths, and weaknesses of the five types of vaccines including live attenuated vaccine, inactivated virus vaccine, recombinant subunit vaccine, viral vectored vaccine, and DNA vaccine. |
format | Online Article Text |
id | pubmed-7159032 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-71590322020-04-21 A Review on Dengue Vaccine Development Deng, Sheng-Qun Yang, Xian Wei, Yong Chen, Jia-Ting Wang, Xiao-Jun Peng, Hong-Juan Vaccines (Basel) Review Dengue virus (DENV) has become a global health threat with about half of the world’s population at risk of infection. Although the disease caused by DENV is self-limiting in the first infection, the antibody-dependent enhancement (ADE) effect increases the mortality in the second infection with a heterotypic virus. Since there is no specific efficient medicine in treatment, it is urgent to develop vaccines to prevent infection and disease progression. Currently, only a live attenuated vaccine, chimeric yellow fever 17D—tetravalent dengue vaccine (CYD-TDV), has been licensed for clinical use in some countries, and many candidate vaccines are still under research and development. This review discusses the progress, strengths, and weaknesses of the five types of vaccines including live attenuated vaccine, inactivated virus vaccine, recombinant subunit vaccine, viral vectored vaccine, and DNA vaccine. MDPI 2020-02-02 /pmc/articles/PMC7159032/ /pubmed/32024238 http://dx.doi.org/10.3390/vaccines8010063 Text en © 2020 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 (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Deng, Sheng-Qun Yang, Xian Wei, Yong Chen, Jia-Ting Wang, Xiao-Jun Peng, Hong-Juan A Review on Dengue Vaccine Development |
title | A Review on Dengue Vaccine Development |
title_full | A Review on Dengue Vaccine Development |
title_fullStr | A Review on Dengue Vaccine Development |
title_full_unstemmed | A Review on Dengue Vaccine Development |
title_short | A Review on Dengue Vaccine Development |
title_sort | review on dengue vaccine development |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7159032/ https://www.ncbi.nlm.nih.gov/pubmed/32024238 http://dx.doi.org/10.3390/vaccines8010063 |
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