NIH-funded research R01 grant

Off-the-shelf immune-compatible stem cells for eye diseases

Official title: Alloimmune-compatible stem cells for ocular diseases

Funded at Schepens Eye Research Institute · NIH-11251986 · Data updated 2026-11-12

Develops ready-made stem cells designed to avoid immune rejection to help people who need cell-based repair for eye conditions.

Quick facts

Grant typeR01 grant
Study typeNIH-funded research
Funding institutionSchepens Eye Research Institute
NIH-funded
Lab location1 site (Boston, United States)
Project startJanuary 1, 2025
Project endDecember 31, 2029
Funding year2026
Award (this year)$492,500
NIH project number5R01EY036033-02
Project IDNIH-11251986 on NIH RePORTER

Who could benefit from this research

Could help

People with retinal degeneration, macular degeneration, corneal injuries, or other eye conditions that might benefit from cell replacement and who would be eligible for future clinical testing.

Less likely to help

Patients with eye problems not treatable by cell replacement (such as simple refractive errors), those with active ocular infection, or those medically ineligible for transplantation may not benefit.

What this research studies

As a patient, this work means scientists are engineering induced pluripotent stem cells (iPSCs) so they can be used in many people without being rejected by the immune system. They plan to make iPSCs express HLA-I molecules that are either peptide-free or loaded with low-affinity peptides to prevent CD8+ T cell attacks while still protecting against natural killer (NK) cell killing. The team will test these engineered cells in the lab and in preclinical models to see whether the cells survive, avoid immune attack, and function like normal eye cells. If preclinical results are promising, the approach could move toward clinical testing for people with retinal or corneal damage.

Why it matters

Potential benefit: Could provide ready-made immune-compatible cells to repair damaged retinal or corneal tissue, shortening wait times and cutting the cost of personalized cell therapies.

How similar studies have gone: Previous lab work using HLA deletion or non-classical HLA expression has shown promise in reducing rejection, but the peptide-free/low-affinity HLA strategy is a newer approach with more limited in vivo testing.

Where this research is happening

  • Schepens Eye Research Institute
    Boston, United States
    Active

Researchers

  • Principal investigator: Chauhan, Sunil K — Schepens Eye Research Institute
  • Study coordinator: Chauhan, Sunil K

Related research

Other NIH-funded projects on the same topics.

About this research

  1. This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
  2. Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
  3. For full project details, budget, and progress reports, visit the official NIH RePORTER page.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.