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Utility, Limitations, and Future of Non-Human Primates for Dengue Research and Vaccine Development

Dengue is considered the most important emerging, human arboviruses, with worldwide distribution in the tropics. Unfortunately, there are no licensed dengue vaccines available or specific anti-viral drugs. The development of a dengue vaccine faces unique challenges. The four serotypes co-circulate i...

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Autores principales: Sariol, Carlos A., White, Laura J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4174039/
https://www.ncbi.nlm.nih.gov/pubmed/25309540
http://dx.doi.org/10.3389/fimmu.2014.00452
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author Sariol, Carlos A.
White, Laura J.
author_facet Sariol, Carlos A.
White, Laura J.
author_sort Sariol, Carlos A.
collection PubMed
description Dengue is considered the most important emerging, human arboviruses, with worldwide distribution in the tropics. Unfortunately, there are no licensed dengue vaccines available or specific anti-viral drugs. The development of a dengue vaccine faces unique challenges. The four serotypes co-circulate in endemic areas, and pre-existing immunity to one serotype does not protect against infection with other serotypes, and actually may enhance severity of disease. One foremost constraint to test the efficacy of a dengue vaccine is the lack of an animal model that adequately recapitulates the clinical manifestations of a dengue infection in humans. In spite of this limitation, non-human primates (NHP) are considered the best available animal model to evaluate dengue vaccine candidates due to their genetic relatedness to humans and their ability to develop a viremia upon infection and a robust immune response similar to that in humans. Therefore, most dengue vaccines candidates are tested in primates before going into clinical trials. In this article, we present a comprehensive review of published studies on dengue vaccine evaluations using the NHP model, and discuss critical parameters affecting the usefulness of the model. In the light of recent clinical data, we assess the ability of the NHP model to predict immunological parameters of vaccine performances in humans and discuss parameters that should be further examined as potential correlates of protection. Finally, we propose some guidelines toward a more standardized use of the model to maximize its usefulness and to better compare the performance of vaccine candidates from different research groups.
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spelling pubmed-41740392014-10-10 Utility, Limitations, and Future of Non-Human Primates for Dengue Research and Vaccine Development Sariol, Carlos A. White, Laura J. Front Immunol Immunology Dengue is considered the most important emerging, human arboviruses, with worldwide distribution in the tropics. Unfortunately, there are no licensed dengue vaccines available or specific anti-viral drugs. The development of a dengue vaccine faces unique challenges. The four serotypes co-circulate in endemic areas, and pre-existing immunity to one serotype does not protect against infection with other serotypes, and actually may enhance severity of disease. One foremost constraint to test the efficacy of a dengue vaccine is the lack of an animal model that adequately recapitulates the clinical manifestations of a dengue infection in humans. In spite of this limitation, non-human primates (NHP) are considered the best available animal model to evaluate dengue vaccine candidates due to their genetic relatedness to humans and their ability to develop a viremia upon infection and a robust immune response similar to that in humans. Therefore, most dengue vaccines candidates are tested in primates before going into clinical trials. In this article, we present a comprehensive review of published studies on dengue vaccine evaluations using the NHP model, and discuss critical parameters affecting the usefulness of the model. In the light of recent clinical data, we assess the ability of the NHP model to predict immunological parameters of vaccine performances in humans and discuss parameters that should be further examined as potential correlates of protection. Finally, we propose some guidelines toward a more standardized use of the model to maximize its usefulness and to better compare the performance of vaccine candidates from different research groups. Frontiers Media S.A. 2014-09-24 /pmc/articles/PMC4174039/ /pubmed/25309540 http://dx.doi.org/10.3389/fimmu.2014.00452 Text en Copyright © 2014 Sariol and White. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Sariol, Carlos A.
White, Laura J.
Utility, Limitations, and Future of Non-Human Primates for Dengue Research and Vaccine Development
title Utility, Limitations, and Future of Non-Human Primates for Dengue Research and Vaccine Development
title_full Utility, Limitations, and Future of Non-Human Primates for Dengue Research and Vaccine Development
title_fullStr Utility, Limitations, and Future of Non-Human Primates for Dengue Research and Vaccine Development
title_full_unstemmed Utility, Limitations, and Future of Non-Human Primates for Dengue Research and Vaccine Development
title_short Utility, Limitations, and Future of Non-Human Primates for Dengue Research and Vaccine Development
title_sort utility, limitations, and future of non-human primates for dengue research and vaccine development
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4174039/
https://www.ncbi.nlm.nih.gov/pubmed/25309540
http://dx.doi.org/10.3389/fimmu.2014.00452
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