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The neuroimmune interface in retinal regeneration
Sucheta Bhattacharya1, Jugasmita Deka1, Thomas Avallone2
1Department of Ophthalmology and Visual Sciences, SUNY Upstate Medical University, Syracuse, NY, 13210, USA; Department of Neuroscience and Physiology, SUNY Upstate Medical University, Syracuse, NY, 13210, USA.
Progress in Retinal and Eye Research
|April 26, 2025
Summary
This review explores the neuroimmune interface in retinal repair, highlighting how immune cells influence neuron regeneration and axonal regrowth. Novel immunomodulatory strategies are proposed to optimize retinal repair and combat blindness.
Area of Science:
- Neuroscience
- Immunology
- Regenerative Medicine
Background:
- Retinal neurodegeneration causes irreversible blindness due to limited neuron regeneration in mammals.
- Current retinal repair strategies include endogenous cell reprogramming and stem cell transplantation.
- A key challenge is promoting axonal regeneration and proper neural connections in the optic nerve.
Purpose of the Study:
- To review the role of the neuroimmune interface in retinal repair.
- To dissect how immune interactions affect glial reprogramming, transplantation, and axonal regeneration.
- To identify immunomodulatory strategies for enhancing retinal regeneration.
Main Methods:
- Literature review integrating findings from regenerative species and mammalian models.
- Analysis of the neuroimmune interactions in the context of retinal degeneration and repair.
- Exploration of immune cell roles in neurogenesis and axonal growth.
Main Results:
- Emerging evidence shows immune cells actively shape neurodegeneration and regeneration.
- Immune interactions critically influence glial reprogramming and stem cell transplantation success.
- Understanding these interactions is key to overcoming barriers in axonal regeneration.
Conclusions:
- The neuroimmune interface is a critical target for optimizing retinal regeneration.
- Immunomodulatory strategies hold promise for treating blindness caused by retinal neurodegeneration.
- Further research integrating immunology and regenerative neuroscience is needed.

