Single Dose Ebola Vaccine is Safe and Effective in Monkeys Against Outbreak Strain

The news item below relates to a study done at Rocky Mountain Laboratories and released today in the journal Science. This is the same vaccine cited in last Friday’s report in The Lancet about a successful human clinical trial in Guinea.




Thursday, Aug. 6, 2015
2:00 p.m. Eastern Time

Single Dose Ebola Vaccine is Safe and Effective in Monkeys against Outbreak Strain
VSV-EBOV Appears to Trigger Innate and Adaptive Immunity

First author Andrea Marzi, Ph.D., of NIAID’s Laboratory of Virology, is shown in August 2014 analyzing Ebola test results from the ELWA3 hospital compound in Monrovia, Liberia.
Credit: NIAID
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National Institutes of Health (NIH) scientists report that a single dose of an experimental Ebola virus (EBOV) vaccine completely protects cynomolgus macaques against the current EBOV outbreak strain, EBOV-Makona, when given at least seven days before exposure, and partially protects them if given three days prior. The live-attenuated vaccine, VSV-EBOV, uses genetically engineered vesicular stomatitis virus (VSV) to carry an EBOV gene that has safely induced protective immunity in macaques. The experimental vaccine is currently undergoing testing in a global clinical trial in humans. VSV, an animal virus that primarily affects cattle, has been successfully tested as an experimental vaccine platform against several viruses.

Prior to this study, scientists had no information about how monkeys vaccinated with VSV-EBOV would respond to a challenge with EBOV-Makona, which has spread throughout West Africa. Previous animal studies demonstrated that VSV-EBOV could successfully protect monkeys against the first EBOV strain recognized, Mayinga, in 1976, and against EBOV-Kikwit, a strain that emerged in Central Africa in 1995. This new study shows that certain immune responses induced by VSV-EBOV are similar against all three viruses. The scientists, from NIH’s National Institute of Allergy and Infectious Diseases Division of Intramural Research, concluded from these findings that VSV-EBOV likely would be equally protective against different EBOV strains.

The group also observed that the experimental VSV-EBOV vaccine appears to provide initial protection by triggering innate virus-fighting host responses; these responses partially protected animals challenged with EBOV-Makona within a week after vaccination. Animals vaccinated more than a week before viral challenge developed antibodies, an adaptive immune response, that were shown to be critical for protection.

A Marzi et al. VSV-EBOV rapidly protects macaques against infection with the 2014/15 Ebola virus outbreak strain. Science DOI: 10.1126/science.aab3920 (2015).

NIAID Director Anthony S. Fauci, M.D., is available to comment on this study as are Heinz Feldmann, M.D., Ph.D., and Andrea Marzi, Ph.D., both experts in viral hemorrhagic fever research in NIAID’s Laboratory of Virology.

To schedule interviews, please contact Ken Pekoc, (301)

NIAID conducts and supports research—at NIH, throughout the United States, and worldwide—to study the causes of infectious and immune-mediated diseases, and to develop better means of preventing, diagnosing and treating these illnesses. News releases, fact sheets and other NIAID-related materials are available on the NIAID website.

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