| Literature DB >> 29553577 |
Lyndon da Cruz1,2,3,4, Kate Fynes1, Odysseas Georgiadis1,2,3, Julie Kerby5,6, Yvonne H Luo1,2,3, Ahmad Ahmado1, Amanda Vernon7, Julie T Daniels7, Britta Nommiste1, Shazeen M Hasan1, Sakina B Gooljar1, Amanda-Jayne F Carr1, Anthony Vugler1, Conor M Ramsden1,3, Magda Bictash5, Mike Fenster5, Juliette Steer5, Tricia Harbinson5, Anna Wilbrey5, Adnan Tufail2,3, Gang Feng5, Mark Whitlock5, Anthony G Robson2,3, Graham E Holder2,3, Mandeep S Sagoo2,3, Peter T Loudon5, Paul Whiting5,8, Peter J Coffey1,2,9.
Abstract
Age-related macular degeneration (AMD) remains a major cause of blindness, with dysfunction and loss of retinal pigment epithelium (RPE) central to disease progression. We engineered an RPE patch comprising a fully differentiated, human embryonic stem cell (hESC)-derived RPE monolayer on a coated, synthetic basement membrane. We delivered the patch, using a purpose-designed microsurgical tool, into the subretinal space of one eye in each of two patients with severe exudative AMD. Primary endpoints were incidence and severity of adverse events and proportion of subjects with improved best-corrected visual acuity of 15 letters or more. We report successful delivery and survival of the RPE patch by biomicroscopy and optical coherence tomography, and a visual acuity gain of 29 and 21 letters in the two patients, respectively, over 12 months. Only local immunosuppression was used long-term. We also present the preclinical surgical, cell safety and tumorigenicity studies leading to trial approval. This work supports the feasibility and safety of hESC-RPE patch transplantation as a regenerative strategy for AMD.Entities:
Mesh:
Year: 2018 PMID: 29553577 DOI: 10.1038/nbt.4114
Source DB: PubMed Journal: Nat Biotechnol ISSN: 1087-0156 Impact factor: 54.908