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University of Oregon researchers develop gene therapy for eye disease
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<span>University of Oregon researchers develop gene therapy for eye disease</span>
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The therapy could eventually provide an alternative treatment for Fuchs’ dystrophy, an eye disease that is the leading cause of corneal transplant surgery
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August 3, 2021
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<a href="/about/news-and-events/news?topic=243" hreflang="en">Corneal Conditions</a>
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<a href="/about/news-and-events/news?topic=401" hreflang="en">Gene Therapy</a>
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<a href="/about/news-and-events/news?topic=402" hreflang="en">Genetics</a>
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<p>Researchers in the Phil and Penny Knight Campus for Accelerating Scientific Impact at the University of Oregon have developed, in mice, a new gene therapy that could eventually provide an alternative treatment for Fuchs’ endothelial corneal dystrophy, a genetic eye disease affecting roughly one in 2,000 people globally. Currently, the only treatment is corneal transplant, a major surgery with associated risks and potential complications.</p><p>“When you do a transplant you make a huge difference for that person, but it's a big deal for the patient with lots of visits, lots of eye drops, lots of co-pays, and if you had a medical treatment that did not require surgery, that would be great,” said Bala Ambati, a research professor in the Knight Campus and corneal surgeon who led an eight-year study involving the development of the gene therapy. “Not only could it help patients who need a transplant, but it could also help a lot of other people who could have used that (corneal) tissue."</p>
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<a href="https://accelerate.uoregon.edu/gene-therapy" class="c-link__link">Read more at the University of Oregon News</a>
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