A single jab can now prevent people from losing their vision, thanks to researchers at Trinity College Dublin, Ireland, who have developed a new method to inject drug into the blood by weakening the otherwise impermeable blood-retina barrier.
The blood-retina barrier normally prevents molecules in the blood from reaching the retina.
Anatomy of the Eye - Animation
Interactive section of Medindia gives details regarding anatomy of the Eye
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Presently, drugs to treat age-related macular degeneration, the leading cause of blindness in the west, have to be injected into the eyeball once a month, which can cause eye infections and even blindness in 1 out of 50 injections.
But now, researchers led by Matthew Campbell have now restored the vision of mice by temporarily weakening the blood-retina barrier to let drug molecules injected into the blood slip through.
![Gene Therapy Helps to Cure Hereditary Blindness]( "Gene Therapy Helps to Cure Hereditary Blindness")
Three patients, who received gene therapy for an inherited form of blindness, continued having vision improvements even after a year, a new study has revealed.
Using a technique called RNA interference (RNAi), they could block the production of claudin-5-a protein that normally helps make the blood-retina barrier impermeable.
"It's proof of principle," New Scientist quoted Campbell as saying.
However, RNAi therapy is not yet safe enough for use in people, as it would breach the blood-brain barrier as well as the blood-retina barrier.
The team are already working on a way to block claudin-5 production in the eye only.
This method involves gene therapy using a modified virus that makes the RNA only in the presence of an antibiotic called doxycycline.
With the novel approach, patients would need only one initial injection into their eye to deliver the virus.
Then once a month they would take the antibiotic orally, and two days later the drug to treat blindness would be injected in their blood.
By then the blood-retina barrier would be sufficiently weakened to allow the drug to pass through.
Although the existing drugs to treat age-related macular degeneration would be too big to pass through the barrier, there are other molecules in development that are small enough.
Some of these could be taken orally when the barrier goes down.
The study has been published in Proceedings of the National Academy of Sciences.
Source: ANI
LIN
Gene Therapy Helps to Cure Hereditary Blindness
Three patients, who received gene therapy for an inherited form of blindness, continued having vision improvements even after a year, a new study has revealed.
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Using a technique called RNA interference (RNAi), they could block the production of claudin-5-a protein that normally helps make the blood-retina barrier impermeable.
"It's proof of principle," New Scientist quoted Campbell as saying.
However, RNAi therapy is not yet safe enough for use in people, as it would breach the blood-brain barrier as well as the blood-retina barrier.
The team are already working on a way to block claudin-5 production in the eye only.
This method involves gene therapy using a modified virus that makes the RNA only in the presence of an antibiotic called doxycycline.
With the novel approach, patients would need only one initial injection into their eye to deliver the virus.
Then once a month they would take the antibiotic orally, and two days later the drug to treat blindness would be injected in their blood.
By then the blood-retina barrier would be sufficiently weakened to allow the drug to pass through.
Although the existing drugs to treat age-related macular degeneration would be too big to pass through the barrier, there are other molecules in development that are small enough.
Some of these could be taken orally when the barrier goes down.
The study has been published in Proceedings of the National Academy of Sciences.
Source: ANI
LIN
Blindness may be Cured by Gene Therapy for Retinal Degeneration
Researchers from Massachusetts General Hospital (MGH) have successfully restored vision in mice with retinal degeneration, using gene therapy - a development that could lead to blindness cure.
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