| Literature DB >> 28554398 |
Britta Nommiste1, Kate Fynes1, Victoria E Tovell1, Conor Ramsden2, Lyndon da Cruz3, Peter Coffey4.
Abstract
Age-related macular degeneration remains the most common cause of blindness in the western world, severely comprising patients' and carers' quality of life and presenting a great cost to the healthcare system. As the disease progresses, the retinal pigmented epithelium (RPE) layer at the back of the eye degenerates, contributing to a series of events resulting in visual impairment. The easy accessibility of the eye has allowed for in-depth study of disease progression in patients, while in vivo studies have facilitated investigations into healthy and diseased RPE. Consequently, a number of research groups are examining different approaches for the replacement of RPE cells in age-related macular degeneration (AMD) patients. This chapter examines some of these initial proof-of-principle studies and goes on to review the use of pluripotent stem cells as a source for RPE replacement in a number of current AMD clinical trials. Finally, we consider just some of the regulatory and manufacturing challenges presented in taking a promising AMD treatment from the research bench into clinical trials in patients, and how to mitigate potential risks early in process development.Entities:
Keywords: Age-related macular degeneration; Retinal disease; Retinal pigmented epithelium
Mesh:
Year: 2017 PMID: 28554398 DOI: 10.1016/bs.pbr.2017.03.003
Source DB: PubMed Journal: Prog Brain Res ISSN: 0079-6123 Impact factor: 2.453