The team, from The Wistar Institute in Philadelphia, US, optimised a shorter, dose-sparing, immunisation regimen and simplified vaccine that can be directly administered into the skin. They targeted a virus surface protein called glycoprotein.
This new approach induced rapid and protective immunity from virus challenges.
"Synthetic non-viral based DNA technology allows for rapid vaccine development by delivery directly into the skin, resulting in consistent, potent and rapid immunity compared to traditional vaccine approaches," said lead researcher David B. Weiner, Director of Wistar's Vaccine and Immunotherapy Center.
In the study, published in the Journal of Infectious Diseases, the team detected antibody levels were equal or higher to those reported for other vaccines currently being evaluated in the clinic.
"The success of intradermal delivery of a low-dose regimen is very encouraging," said Ami Patel, Ph.D., associate staff scientist in the Weiner Lab. "The ultimate goal of our work is to create effective and safe vaccines that are optimised for field use in at-risk areas."
First discovered in humans in 1976 in the Democratic Republic of the Congo, the largest outbreak occurred in West Africa from 2014 to 2016, which claimed more than 11,000 lives, according to the World Health Organization.
The death rate is about 50 per cent and the virus is spread by contact with contaminated body fluids, including blood and semen.
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