Listen to this page using ReadSpeaker

A Change in Identity Might Someday Save Vision


No, people with inherited retinal diseases don’t have to adopt new names or personas, or go into witness protection programs, to save their vision. But by changing the identity of cells in the retina — namely rods — researchers may someday be able to slow or halt vision loss for those with retinitis pigmentosa (RP) and other related conditions.

While the innovative therapeutic approach is not ready to be tested in humans, a research team led by Tom Reh, PhD, University of Washington, and Sheng Ding, PhD, University of California, San Francisco, accomplished the feat in mice with RP. The investigators treated rods in the mice with a compound known as photoregulin1 (PR1) that blocked a gene involved in rod development called Nr2e3. That, in turn, reduced the expression (activity) of other rod-associated genes, making the rods less rod-like and more like cones. Doing so stopped retinal degeneration, preserving both rods and cones. Rods and cones are important, because they’re the cells that make vision possible. Results of the PR1 study were published online in the journal Investigative Ophthalmology & Visual Science.

Drs. Reh and Ding, along with their colleagues Paul Nakamura, PhD, and Shibing Tang, PhD, targeted rods because they’re the photoreceptors that degenerate first in RP and some other retinal diseases. Most gene mutations that cause RP affect rod function and health. Because cones depend on rods for survival, cones die off as rods are lost. Therefore, saving rods should save cones.

There is a downside to PR1 therapy: Though the converted rods survive, they no longer process light to provide rod-mediated vision. However, the converted rods preserve existing cones. By saving cones, the therapy would maintain the patient’s central and color vision and vision in bright settings, as well as the ability to perceive details (i.e., read, drive, and recognize faces). With the loss of rod-mediated vision, the therapy recipient’s night and peripheral vision would be significantly reduced.

Dr. Reh notes that much more work in chemistry needs to be done to develop PR1 into an oral compound that could be taken by people in a clinical trial.

“I think this approach has the potential to help anyone who still has rods left in their retinas,” says Dr. Reh. “We were pleased that PR1 worked in mice with a mutation in RHO, which causes autosomal dominant RP, and a mutation in PDE6β, which causes autosomal recessive RP. We would like to test the compound in a variety of retinal-disease models to see how broad the efficacy is.”

Please follow and like us:

10 Responses to 'A Change in Identity Might Someday Save Vision'

  1. Ranga Rao Veeravalli says:

    I am from India, would like to know treatment for RP. My daughter have RP. She is 18years old. Right eye started blurring. Please guide me in this regard.

  2. douglas says:

    Someday? You know Gordon and his Foundation have pumped millions of dollars for research over 5 decades and really not much progress have been made. There are a lot of fine folks out there with the crippling eye diseases and losing sight on a daily basis. We are tired of hearing words like maybe, someday, might, etc. from researchers. You know Gordon is getting up there in age and I’m sure he would be able to see before he passes.

  3. Dennis McGowan says:

    When and if you are ready for human studies please let me know i would be up for the trial. My daughter also has it as does mu mother.

  4. Sandy says:

    This gives hope to future generations! Our granddaughter received the diagnosis ten years ago. She is 15 now and is doing very well. I understand the urgency expressed by others. It is often more than I can bare to think of this beautiful, active young lady losing her sight. All things are normal for her now because her parents are not telling her what the future holds yet. My prayer is that science will find a cure for my granddaughter and others who suffer from this terrible disease. This sounds like a step in the right direction. I am certain those suffering from RP would quickly say yes to maintaining most of they sight they still have.

  5. Judy says:

    My daughter is 35 and has RP. For anyone that has this diease, a cure can’t come fast enough. Our hope with alot of prayers, as well as doing the Vision Walks (this is our 10th year) and raising alot of research dollars, is that we can help with speeding up the process! Good luck to everyone going through this. My heart goes out to all of you.

  6. Mary Deuss says:

    Dear Doctor;
    I am a healthy 59 year old female with inherited RP. My father had RP as does 3 of my other siblings. I searched online for a study to enroll without success. Please contact me if you know of any studies near Cincinnati Ohio. Thank you and God bless you.

  7. masterduke says:

    very very thanks
    i hope ….

Leave a Reply

Your email address will not be published. Required fields are marked *