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Human antibody response to dengue virus: implications for dengue vaccine design

Dengue, a global health threat, is a leading cause of morbidity and mortality in most tropical and subtropical countries. Dengue can range from asymptomatic, relatively mild dengue fever to severe and life-threatening dengue hemorrhagic fever. Disease severity and outcome is largely associated with...

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Detalles Bibliográficos
Autores principales: Moi, Meng Ling, Takasaki, Tomohiko, Kurane, Ichiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4934144/
https://www.ncbi.nlm.nih.gov/pubmed/27398060
http://dx.doi.org/10.1186/s41182-016-0004-y
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author Moi, Meng Ling
Takasaki, Tomohiko
Kurane, Ichiro
author_facet Moi, Meng Ling
Takasaki, Tomohiko
Kurane, Ichiro
author_sort Moi, Meng Ling
collection PubMed
description Dengue, a global health threat, is a leading cause of morbidity and mortality in most tropical and subtropical countries. Dengue can range from asymptomatic, relatively mild dengue fever to severe and life-threatening dengue hemorrhagic fever. Disease severity and outcome is largely associated with the host immune response. Several candidate vaccines in clinical trials appear promising as effective measures for dengue disease control. Vaccine development has been hampered by safety and efficacy issues, driven by a lack of understanding of the host immune response. This review focuses on recent research findings on the dengue host immune response, particularly in humans, and the relevance of these findings to challenges in vaccine development.
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spelling pubmed-49341442016-07-08 Human antibody response to dengue virus: implications for dengue vaccine design Moi, Meng Ling Takasaki, Tomohiko Kurane, Ichiro Trop Med Health Review Dengue, a global health threat, is a leading cause of morbidity and mortality in most tropical and subtropical countries. Dengue can range from asymptomatic, relatively mild dengue fever to severe and life-threatening dengue hemorrhagic fever. Disease severity and outcome is largely associated with the host immune response. Several candidate vaccines in clinical trials appear promising as effective measures for dengue disease control. Vaccine development has been hampered by safety and efficacy issues, driven by a lack of understanding of the host immune response. This review focuses on recent research findings on the dengue host immune response, particularly in humans, and the relevance of these findings to challenges in vaccine development. BioMed Central 2016-03-14 /pmc/articles/PMC4934144/ /pubmed/27398060 http://dx.doi.org/10.1186/s41182-016-0004-y Text en © Moi et al 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Moi, Meng Ling
Takasaki, Tomohiko
Kurane, Ichiro
Human antibody response to dengue virus: implications for dengue vaccine design
title Human antibody response to dengue virus: implications for dengue vaccine design
title_full Human antibody response to dengue virus: implications for dengue vaccine design
title_fullStr Human antibody response to dengue virus: implications for dengue vaccine design
title_full_unstemmed Human antibody response to dengue virus: implications for dengue vaccine design
title_short Human antibody response to dengue virus: implications for dengue vaccine design
title_sort human antibody response to dengue virus: implications for dengue vaccine design
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4934144/
https://www.ncbi.nlm.nih.gov/pubmed/27398060
http://dx.doi.org/10.1186/s41182-016-0004-y
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