4.3 Review

Autologous stem cell therapy for inherited and acquired retinal disease

Journal

REGENERATIVE MEDICINE
Volume 13, Issue 1, Pages 89-96

Publisher

FUTURE MEDICINE LTD
DOI: 10.2217/rme-2017-0089

Keywords

autologous; induced pluripotent stem cells; retinal degeneration; stem cell

Funding

  1. National Institute of Health [5P30EY019007, R01EY018213, R01EY024698, R01EY026682, R21AG050437]
  2. National Cancer Institute Core [5P30CA013696]
  3. Research to Prevent Blindness (RPB) Physician-Scientist Award
  4. RPB, New York, NY, USA
  5. RPB Medical Student Eye Research Fellowship
  6. Tistou and Charlotte Kerstan Foundation
  7. Schneeweiss Stem Cell Fund, New York State [C029572]
  8. Foundation Fighting Blindness New York Regional Research Center Grant [C-NY05-0705-0312]
  9. Crowley Family Fund
  10. Gebroe Family Foundation

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The mammalian retina, derived from neural ectoderm, has little regenerative potential. For conditions where irreversible retinal pigment epithelium or photoreceptor cell loss occurs, advanced techniques are required to restore vision. Inherited retinal dystrophies and some acquired conditions, such as age-related macular degeneration, have a similar end result of photoreceptor cell death leading to debilitating vision loss. These diseases stand to benefit from future regenerative medicine as dietary recommendations and current pharmacologic therapy only seek to prevent further disease progression. Cell-based strategies, such as autologously derived induced pluripotent stem cells, have come a long way in overcoming previous technical and ethical concerns. Clinical trials for such techniques are already underway. These trials and the preceding preclinical studies will be discussed in the context of retinal disease.

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