Allogeneic Ex Vivo Expanded Corneal Epithelial Stem Cell Transplantation: A Randomized Controlled Clinical Trial

Author:

Campbell John D.M.1,Ahmad Sajjad2,Agrawal Ashish3,Bienek Carol1,Atkinson Anne1,Mcgowan Neil W.A.1,Kaye Stephen2,Mantry Sanjay4,Ramaesh Kanna4,Glover Alison1,Pelly Jane1,MacRury Coral1,MacDonald Margaret3,Hargreaves Emily1,Barry Jacqueline1,Drain John1,Cuthbertson Bruce1,Nerurkar Louis5,Downing Ian1,Fraser Alasdair R.1,Turner Marc L.1,Dhillon Baljean3

Affiliation:

1. Scottish National Blood Transfusion Service, Edinburgh, United Kingdom

2. Royal Liverpool and Broadgreen University Hospitals St. Paul’s Eye Unit, Liverpool, United Kingdom

3. Princess Alexandra Eye Pavillion, Edinburgh, United Kingdom

4. Tennent Institute of Opthalmology, Gartnavel General Hospital, Glasgow, United Kingdom

5. Institute of Infection, Immunity, and Inflammation University of Glasgow, Glasgow, United Kingdom

Abstract

Abstract Limbal stem cell deficiency (LSCD) is a disease resulting from the loss or dysfunction of epithelial stem cells, which seriously impairs sight. Autologous limbal stem cell transplantation is effective in unilateral or partial bilateral disease but not applicable in total bilateral disease. An allogeneic source of transplantable cells for use in total bilateral disease can be obtained from culture of donated cadaveric corneal tissue. We performed a controlled multicenter study to examine the feasibility, safety, and efficacy of allogeneic corneal epithelial stem cells in the treatment of bilateral LSCD. Patients were randomized to receive corneal epithelial stem cells cultured on amniotic membrane (AM): investigational medicinal product (IMP) or control AM only. Patients received systemic immunosuppression. Primary endpoints were safety and visual acuity, secondary endpoint was change in composite ocular surface score (OSS). Sixteen patients were treated and 13 patients completed all assessments. Safety was demonstrated and 9/13 patients had improved visual acuity scores at the end of the trial, with no significant differences between IMP and control groups. Patients in the IMP arm demonstrated significant, sustained improvement in OSS, whereas those in the control arm did not. Serum cytokine levels were measured during and after the period of immune suppression and we identified strongly elevated levels of CXCL8 in the serum of patients with aniridia, which persisted throughout the trial. This first randomized control trial of allogeneic corneal epithelial stem cells in severe bilateral LSCD demonstrates the feasibility and safety of this approach. tem Cells Translational Medicine  2019;8:323–331

Funder

Scottish Enterprise

UK Stem Cell Foundation

Scottish Chief Scientist’s Office

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,General Medicine

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