Researchers at KAIST have developed a groundbreaking drug for retinal nerve regeneration to restore vision loss.
The new therapy targets the PROX1 protein to induce retinal regeneration and achieve significant vision recovery in disease-model mice.
Importantly, the induced neural regeneration in mammalian retinas offers hope for patients with currently limited treatment options.
Inspired by aquatic wildlife, the researchers identified PROX1 as a key obstacle in facilitating Müller glia cell dedifferentiation for retinal repair.
A proposed antibody treatment disrupts PROX1's inhibitory function, promoting Müller glia migration and visual function restoration.
This innovative therapy shows promise for degenerative retinal diseases and may undergo clinical trials by 2028.
The collaborative efforts of KAIST researchers and Celliaz Inc. aim to provide effective solutions for retinal disorders.
The research, published in Nature Communications, emphasizes hope for individuals affected by vision loss.
The study underscores the commitment to advancing medical science and offering viable treatment avenues for retinal diseases.
This breakthrough signifies a significant step towards addressing global vision loss challenges and restoring sight to millions.