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Σάββατο 18 Νοεμβρίου 2017

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

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

Expert Opin Biol Ther. 2017 Nov 17;:1-15

Authors: Wong G, Mendoza EJ, Plummer FA, Gao GF, Kobinger GP, Qiu X

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.

PMID: 29148858 [PubMed - as supplied by publisher]



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