| Literature DB >> 25814063 |
Andrea Marzi1, Peter Halfmann2, Lindsay Hill-Batorski2, Friederike Feldmann3, W Lesley Shupert1, Gabriele Neumann2, Heinz Feldmann1, Yoshihiro Kawaoka4.
Abstract
Zaire ebolavirus is the causative agent of the current outbreak of hemorrhagic fever disease in West Africa. Previously, we showed that a whole Ebola virus (EBOV) vaccine based on a replication-defective EBOV (EBOVΔVP30) protects immunized mice and guinea pigs against lethal challenge with rodent-adapted EBOV. Here, we demonstrate that EBOVΔVP30 protects nonhuman primates against lethal infection with EBOV. Although EBOVΔVP30 is replication-incompetent, we additionally inactivated the vaccine with hydrogen peroxide; the chemically inactivated vaccine remained antigenic and protective in nonhuman primates. EBOVΔVP30 thus represents a safe, efficacious, whole-EBOV vaccine candidate that differs from other EBOV vaccine platforms in that it presents all viral proteins and the viral RNA to the host immune system, which might contribute to protective immune responses.Entities:
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Year: 2015 PMID: 25814063 PMCID: PMC4565490 DOI: 10.1126/science.aaa4919
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728