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The researchers knew they could halt and even reverse the condition by suppressing an overactive protein called vascular endothelial growth factor (VEGF). Other researchers had been able to do it with monthly eye injections, but this team was hoping to do it with just one injection.
The best way they found to do this was by using a common cold-like virus called AAV2 as a carrier of gene that activates the production of a different protein, sFLT01, to counter VEGF.
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The clinical trial showed promising results, with the condition of four of the patients improving dramatically after just one viral injection. [T]he treatment didn’t produce any side effects in any patients, either. “Even at the highest dose, the treatment was quite safe. We found there were almost no adverse reactions in our patients,” said researcher Peter Campochiaro.
[Read the original source here]The GLP aggregated and excerpted this blog/article to reflect the diversity of news, opinion, and analysis. Read full, original post: An Experimental Gene Therapy Uses Viruses to Stop Age-Related Blindness