Gene therapy showed promising results to help blind monkeys regain their vision. This finding could be applied to humans in near future.

Luk Vandenberghe at the University of Pennsylvania in Philadelphia, and colleagues tried to find out whether it would be possible to deliver genes that would eventually restore photoreceptor cells, reports New Scientist.
They used two adeno-associated viruses, called AAV2 and AAV8, to deliver genes into monkey retinas.
The viruses were marked with a green fluorescent protein. By monitoring the green markers, the researchers were able to assess the minimum dose at which the viruses could deliver working genes into the retinal cells.
A dose of AAV8 performed best, presenting an important step in using gene therapy to treat and restore photoreceptor cells in humans.
The study has been published in Science Translational Medicine.
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