New AAV Gene Therapy to Treat and Prevent Ebola Infection

by Anjali Aryamvally on  March 8, 2018 at 10:30 AM Genetics & Stem Cells News
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An innovative antibody delivery method delivers a monoclonal antibody gene to a cell using a viral vector called adeno-associated virus (AAV) and provides up to 100% protection against Ebola infection in mice.
New AAV Gene Therapy to Treat and Prevent Ebola Infection
New AAV Gene Therapy to Treat and Prevent Ebola Infection

More than 11,000 people died during the Ebola outbreak in West Africa from 2013-16, demonstrating both the deadly nature of the virus and the limitations of the medication used to fight it.

The mice expressed the antibody for more than 300 days, revealed the study appearing in the Journal of Infectious Diseases.

"If you use an AAV gene therapy vector to deliver the DNA blueprint to a cell, that cell will produce a protective antibody against Ebola virus, which is then secreted into the bloodstream and protects mice from infection," said Sarah Wootton, Professor at the University of Guelph in Ontario, Canada.

Once the antibody gene is delivered, antibodies will be continually produced in the bloodstream.

"We are hoping to use this technology in a post-exposure scenario. Let's say someone has been exposed to Ebola. The idea would be to give them this AAV vector to start producing the antibodies that prevent death," Wootton noted.

Other researchers have used AAV extensively to treat a variety of genetic disorders.

The US Food and Drug Administration has recently approved an AAV gene therapy to treat a rare retinal disorder.



Source: IANS

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