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From bench to almost bedside: the long road to a licensed Ebola virus vaccine.


ABSTRACT: INTRODUCTION:The Ebola virus (EBOV) disease epidemic during 2014-16 in West Africa has accelerated the clinical development of several vaccine candidates that have demonstrated efficacy in the gold standard nonhuman primate (NHP) model, namely cynomolgus macaques. AREAS COVERED:This review discusses the pre-clinical research and if available, clinical evaluation of the currently available EBOV vaccine candidates, while emphasizing the translatability of pre-clinical data generated in the NHP model to clinical data in humans. EXPERT OPINION:Despite the existence of many successful EBOV vaccine candidates in the pre-clinical stages, only two platforms became the focus of Phase 2/3 efficacy trials in Liberia, Sierra Leone, and Guinea near the peak of the epidemic: the Vesicular stomatitis virus (VSV)-vectored vaccine and the chimpanzee adenovirus type 3 (ChAd3)-vectored vaccine. The results of three distinct clinical trials involving these candidates may soon pave the way for a licensed, safe and efficacious EBOV vaccine to help combat future epidemics.

SUBMITTER: Wong G 

PROVIDER: S-EPMC5841470 | biostudies-literature | 2018 Feb

REPOSITORIES: biostudies-literature

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From bench to almost bedside: the long road to a licensed Ebola virus vaccine.

Wong Gary G   Mendoza Emelissa J EJ   Plummer Francis A FA   Gao George F GF   Kobinger Gary P GP   Qiu Xiangguo X  

Expert opinion on biological therapy 20171117 2


<h4>Introduction</h4>The Ebola virus (EBOV) disease epidemic during 2014-16 in West Africa has accelerated the clinical development of several vaccine candidates that have demonstrated efficacy in the gold standard nonhuman primate (NHP) model, namely cynomolgus macaques.<h4>Areas covered</h4>This review discusses the pre-clinical research and if available, clinical evaluation of the currently available EBOV vaccine candidates, while emphasizing the translatability of pre-clinical data generated  ...[more]

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