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Induced Pluripotent Stem Cells (iPSCs)

Last medically reviewed: October 7, 2026

Induced pluripotent stem cells are adult cells — such as skin or blood cells — reprogrammed in the laboratory into a pluripotent state. The technique was first reported in 2006.

Research is not treatment. The studies summarized below are investigational. They are presented for education only, do not show that any approach is safe or effective in patients, and are not a recommendation. Unless stated as FDA-approved, none of these approaches is approved for this condition. RUO materials are not for human use.

Why iPSCs matter in vision research

They allow researchers to grow a person's own retinal cell types in the laboratory, to model inherited eye disease, and to test drug candidates in human cells.[1]

Human research

A widely cited 2017 report described transplantation of iPSC-derived RPE cells in a person with neovascular AMD. It is a single-patient report, not proof of benefit.[2]

Open questions

Manufacturing consistency, genetic stability, immune compatibility and long-term safety remain active research questions.

Regulatory status: to our knowledge as of our last review, no product in this category is FDA-approved to treat an eye disease. The FDA has warned the public about unapproved stem cell and exosome products.

Answers

Related conditions

Frequently Asked Questions

Are iPSC treatments available for eye disease?

Not as approved treatments. iPSC-derived cells have been studied in early-phase research.

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References

  1. Takahashi K, Yamanaka S. Induction of pluripotent stem cells from mouse embryonic and adult fibroblast cultures by defined factors. Cell, 2006. [Peer-reviewed study · citation details pending reviewer confirmation]
  2. Mandai M, et al. Autologous Induced Stem-Cell–Derived Retinal Cells for Macular Degeneration. New England Journal of Medicine, 2017. [Peer-reviewed study · citation details pending reviewer confirmation]