A Phase I trial with the virus-based prophylactic carried by chimps showed it was "well-tolerated" by 20 healthy adults who generated antibodies and immune cells in response -- though this did not mean they were protected.
The work was "encouraging," epidemiologist Rodolphe Thiebaut of France's Institute of Health and Medical Research (Inserm) said of the candidate vaccine dubbed cAd3-ZEBOV.
But "we still don't have formal proof that the vaccine will work," he told AFP.
"We don't know if the immunity seen in vaccinated people is protective, nor if the other vaccines in development will perform better," said Jonathan Ball, virology professor at the University of Nottingham in England.
CAd3-ZEBOV and other vaccines candidates have yet to cross several hurdles before this will become clear.
Safety having been established in healthy volunteers, Phase II and Phase III clinical trials will determine, in larger groups of infected people, whether the vaccine actually works -- and at which dose.
There is no licenced drug against the deadly haemorrhagic fever-causing virus which is transmitted through bodily fluids.
Developed by the US National Institute of Allergy and Infectious Diseases (NIAID) and drug firm GlaxoSmithKline, cAd3-ZEBOV is based on a chimp adenovirus to which an Ebola virus gene has been added to stimulate an immune response.
The NIAID said yesterday a decision on further trials with the vaccine would depend on data from ongoing Phase I tests with volunteers also at the University of Oxford and in Mali.
The other leading prototype, VSV-ZEBOV manufactured by the Public Health Agency of Canada, uses a weakened livestock disease virus of which a gene has been replaced by an Ebola virus gene.
It is also in Phase I safety trials, and pharma company Merck recently announced it would scale up production.
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