ESCRS - PO771 - Corneal Stem Cell Therapy In Advanced Keratoconus

Corneal Stem Cell Therapy In Advanced Keratoconus

Published 2024 - 42nd Congress of the ESCRS

Reference: PO771 | Type: Free paper | DOI: 10.82333/jx40-as29

Authors: Ceren Ece Semiz* 1 , Faruk Semiz 1 , Gamze Tanrıverdi 2 , Merjem Purelku 2 , Njomza Hima Musa 1 , Fetih Furkan Arslan 3

1Ophthalmology,Eye Hospital,Prishtina,Kosovo, 2Histology and Embryology,Istanbul University-Cerrahpaşa,Istanbul,Türkiye, 3Ophthalmology,Istanbul University-Cerrahpaşa,Istanbul,Türkiye

Purpose

To investigate the new intrastromal histological structures and stem cells that develop after myopic human lenticular intrastromal keratoplasty in keratoconus with femtosecond laser-assisted small incision lenticule extraction (SMILE) surgery by transmission electron microscopy and immunofluorescence studies.

Setting

Eye Hospital, Prishtina, Kosovo

Methods

Fifty eyes with advanced keratoconus indicated for corneal transplantation were included in this study. Fresh myopic lenticular implants were placed in all eyes through SMILE surgery. Lenticular implants were extracted from patients with myopic refractive errors of the cornea,  untreated keratoconus and treated keratoconus following 1, 2, 3,4, and 5 years of surgery. These seven lenticular samples were examined under the electron microscope, immunofluorescence, and compared.

 

Results

Healthy keratocytes, stem cells, and telocyte-like cells were observed in samples obtained five years after intrastromal lenticular keratoplasty. The preoperative CDVA improved from 0.84 ± 0.22 logMAR to 0.45 ± 0.09 logMAR (P< .001). The preoperative CCT increased from 394 ± 13.19 μm to 485.10 ± 8.16 μm (P< .001).

Conclusions

 We believe that future studies will establish the effectiveness of using intrastromal FML keratoplasty in treating advanced keratoconus and other corneal diseases that cause degenerative, progressive, and irregular astigmatism. FML comprising live stem cells, telocytes, and keratocytes is an application of stem cell treatment. 

 

(Clinical Trial Registration Number: NCT04591587)