Zika vaccines and therapeutics: landscape analysis and challenges ahead

Abstract Background Various Zika virus (ZIKV) vaccine candidates are currently in development. Nevertheless, unique challenges in clinical development and regulatory pathways may hinder the licensure of high-quality, safe, and effective ZIKV vaccines. Discussion Implementing phase 3 efficacy trials...

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Main Authors: Annelies Wilder-Smith, Kirsten Vannice, Anna Durbin, Joachim Hombach, Stephen J. Thomas, Irani Thevarjan, Cameron P. Simmons
Format: Article
Language:English
Published: BMC 2018-06-01
Series:BMC Medicine
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12916-018-1067-x
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spelling doaj-ff6ef41735c340e6a0425d1fd46ce0672020-11-25T01:49:10ZengBMCBMC Medicine1741-70152018-06-0116111510.1186/s12916-018-1067-xZika vaccines and therapeutics: landscape analysis and challenges aheadAnnelies Wilder-Smith0Kirsten Vannice1Anna Durbin2Joachim Hombach3Stephen J. Thomas4Irani Thevarjan5Cameron P. Simmons6Immunization, Vaccines & Biologicals, World Health OrganizationImmunization, Vaccines & Biologicals, World Health OrganizationCenter for Immunization Research, Johns Hopkins Bloomberg School of Public HealthImmunization, Vaccines & Biologicals, World Health OrganizationState University of New York, Upstate Medical UniversityDoherty Institute for Infection and ImmunityOxford University Clinical Research UnitAbstract Background Various Zika virus (ZIKV) vaccine candidates are currently in development. Nevertheless, unique challenges in clinical development and regulatory pathways may hinder the licensure of high-quality, safe, and effective ZIKV vaccines. Discussion Implementing phase 3 efficacy trials will be difficult given the challenges of the spatio-temporal heterogeneity of ZIKV transmission, the unpredictability of ZIKV epidemics, the broad spectrum of clinical manifestations making a single definite endpoint difficult, a lack of sensitive and specific diagnostic assays, and the need for inclusion of vulnerable target populations. In addition to a vaccine, drugs for primary prophylaxis, post-exposure prophylaxis, or treatment should also be developed to prevent or mitigate the severity of congenital Zika syndrome. Conclusion Establishing the feasibility of immune correlates and/or surrogates are a priority. Given the challenges in conducting phase 3 trials at a time of waning incidence, human challenge trials should be considered to evaluate efficacy. Continued financial support and engagement of industry partners will be essential to the successful development, licensure, and accessibility of Zika vaccines or therapeutics.http://link.springer.com/article/10.1186/s12916-018-1067-xZikaZika vaccinesFlavivirusAnti-viralsProphylaxisTherapeutics
collection DOAJ
language English
format Article
sources DOAJ
author Annelies Wilder-Smith
Kirsten Vannice
Anna Durbin
Joachim Hombach
Stephen J. Thomas
Irani Thevarjan
Cameron P. Simmons
spellingShingle Annelies Wilder-Smith
Kirsten Vannice
Anna Durbin
Joachim Hombach
Stephen J. Thomas
Irani Thevarjan
Cameron P. Simmons
Zika vaccines and therapeutics: landscape analysis and challenges ahead
BMC Medicine
Zika
Zika vaccines
Flavivirus
Anti-virals
Prophylaxis
Therapeutics
author_facet Annelies Wilder-Smith
Kirsten Vannice
Anna Durbin
Joachim Hombach
Stephen J. Thomas
Irani Thevarjan
Cameron P. Simmons
author_sort Annelies Wilder-Smith
title Zika vaccines and therapeutics: landscape analysis and challenges ahead
title_short Zika vaccines and therapeutics: landscape analysis and challenges ahead
title_full Zika vaccines and therapeutics: landscape analysis and challenges ahead
title_fullStr Zika vaccines and therapeutics: landscape analysis and challenges ahead
title_full_unstemmed Zika vaccines and therapeutics: landscape analysis and challenges ahead
title_sort zika vaccines and therapeutics: landscape analysis and challenges ahead
publisher BMC
series BMC Medicine
issn 1741-7015
publishDate 2018-06-01
description Abstract Background Various Zika virus (ZIKV) vaccine candidates are currently in development. Nevertheless, unique challenges in clinical development and regulatory pathways may hinder the licensure of high-quality, safe, and effective ZIKV vaccines. Discussion Implementing phase 3 efficacy trials will be difficult given the challenges of the spatio-temporal heterogeneity of ZIKV transmission, the unpredictability of ZIKV epidemics, the broad spectrum of clinical manifestations making a single definite endpoint difficult, a lack of sensitive and specific diagnostic assays, and the need for inclusion of vulnerable target populations. In addition to a vaccine, drugs for primary prophylaxis, post-exposure prophylaxis, or treatment should also be developed to prevent or mitigate the severity of congenital Zika syndrome. Conclusion Establishing the feasibility of immune correlates and/or surrogates are a priority. Given the challenges in conducting phase 3 trials at a time of waning incidence, human challenge trials should be considered to evaluate efficacy. Continued financial support and engagement of industry partners will be essential to the successful development, licensure, and accessibility of Zika vaccines or therapeutics.
topic Zika
Zika vaccines
Flavivirus
Anti-virals
Prophylaxis
Therapeutics
url http://link.springer.com/article/10.1186/s12916-018-1067-x
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