Decellularised Corneal Stromal Lamina With or Without Autologous Adipose‐Derived Adult Stem Cells for Advanced Keratoconus: 1‐Year Results of a Phase I/ IIa Clinical Trial

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Authors: Hao Zhang, Jorge L. Alio del Barrio, Alejandra E. Rodriguez, Rafael I. Barraquer, Francisco Arnalich-Montiel, David Mingo‐Botín, María Eugenia Fernández‐Santos, JORGE LUCIANO ALIO
Cited by: 1
References: 43

Abstract

BACKGROUND: To report the 1-year clinical outcomes of decellularised human corneal stromal lamina implantation, with or without autologous adipose-derived adult stem cells (ADASCs), for advanced keratoconus in a European cohort. METHODS: additional ADASCs injected into the stromal pocket (G-2; n = 5). All procedures used femtosecond laser-assisted 9.5-mm intrastromal dissection. RESULTS: No major intraoperative complications occurred except one G-2 micro-tear that resolved. No clinically relevant inflammation, rejection, or graft failure was observed; transparency was restored in all eyes by 3-6 months. At 12 months, central corneal thickness increased by 118.4 μm in G-1 and 121.2 μm in G-2. Decimal UDVA improved by 2.14 ± 0.71 lines in G-1 and 1.30 ± 0.84 lines in G-2; decimal CDVA improved by 2.48 ± 0.66 and 1.43 ± 0.53 lines, respectively. Manifest sphere improved to -1.10 D in G-1 and -0.58 D in G-2, whereas manifest cylinder changed minimally in both groups. Keratometric indices remained largely unchanged. In vivo confocal microscopy demonstrated progressive cellular repopulation of the implanted lamina during follow-up in both groups. CONCLUSIONS: Decellularised stromal lamina implantation, with or without autologous ADASCs, was safe and feasible, maintaining corneal transparency and producing sustained stromal thickening with clinically meaningful visual and refractive improvement at 12 months. Larger adequately powered studies with longer follow-up are required to assess clinical efficacy.

Fields of Study & Subjects

Corneal surgery and disorders Corneal Surgery and Treatments Ocular Surface and Contact Lens

Publication details

Journal / source
Clinical and Experimental Ophthalmology
Publisher
Wiley
Volume
54
Issue
7
Pages
883-894
Publication date
7 July 2026
Language
EN