Completed Digestion, Kidneys & Other Organs Cells, Biochemistry & Physiology

Scalable production of RPE cells from induced pluripotent stem cell under GMP conditions for cellular replacement therapy of the dry form of AMD

In plain English

AI plain-English summary

A skin biopsy could one day supply the cells needed to halt a patient’s progressing blindness. Age-related macular degeneration (AMD) destroys the retinal pigment epithelial (RPE) cells that keep the eye’s light-sensitive photoreceptors alive. Without these support cells, central vision fades and eventually disappears. No treatment currently prevents AMD, and existing interventions work only for some patients and often only temporarily. This project aims to turn a patient’s own skin cells into induced pluripotent stem cells, then coax those stem cells into healthy RPE cells under strict manufacturing standards. Over three years, the team will develop and test the safety and efficacy of these lab-grown cells, preparing them for surgical transplantation. If successful, the therapy could stabilise or restore central vision in the majority of AMD patients—not by slowing the disease, but by replacing the cells that are lost. The immediate goal is to submit a Phase I/II clinical trial application at the end of the project. This is not fundamental science; it is a direct push toward a surgical therapy for a condition that blinds millions.

View original technical description
Age related macular degeneration (AMD) is the leading cause of blindness in people over the age of 60 in the western world and each year the problem increases. AMD results in the central portion of vision being lost making it impossible to appreciate fine detail. AMD is associated with defects of the retinal support cells - the retinal pigment epithelial cells (RPE). The rods and cones (the photoreceptors) in the retina, which are the light sensitive cells, depend for their survival on the normal functioning of these cells, and so failure of these cells leads to progressive loss of vision and eventual blindness. There is currently no treatment which prevents the development of AMD. However there has been some success for certain forms of AMD with a range of interventions, but these approaches are only suitable for certain patients and are often only temporary. Our aim is to produce a cell replacement therapy from stem cells derived from patients themselves which are effective in replacing dysfunctional RPE found in AMD which will lead to a surgical therapy capable of stabalising and restoring vision in the vast majority of patients. We plan to develop, over three years, the necessary process of producing stem cells derived from patient skin samples and to turn these stem cells into RPE. We will test the safety and efficacy of these cells ready for use in patients. The goal is to submit a clinical trial application at the end of this project for these patient derived eye cells to initiate a Phase I/II clinical trial.

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Researchers

Amit Nathwani (Co-Investigator)David Linch (Co-Investigator)Lyndon Da Cruz (Co-Investigator)Peter Coffey (Principal Investigator)Tariq Enver (Co-Investigator)

Related Research

Grants with similar aims, by meaning.

Stem cell based treatment strategy for Age-related Macular Degeneration (AMD)
Synthetic Bruch’s Membranes for Cell Replacement Therapy in Age Related Macular Degeneration
Using cell surface antigens for the isolation of photoreceptor precursor cells for retinal stem cell therapy
Development of a clinically relevant prototype cell transfer sheet (CTS) to act as an artificial Bruchs membrane in the treatment of Age related Macular Degeneration (AMD)
Using cell surface antigens for the isolation of human photoreceptor precursor cells for retinal stem cell therapy

Original classification

Research Grant

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