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Stem Cell Therapy for Corneal Epithelium Regeneration following Good Manufacturing and Clinical Procedures

Objective. To evaluate outcomes of cultivated limbal epithelial transplantation (CLET) for management of ocular surface failure due to limbal stem cell deficiency (LSCD). Design. Prospective, noncomparative, interventional case series and extensive comparison with recent similar studies. Participant...

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Autores principales: Ramírez, Beatriz E., Sánchez, Ana, Herreras, José M., Fernández, Itziar, García-Sancho, Javier, Nieto-Miguel, Teresa, Calonge, Margarita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4588357/
https://www.ncbi.nlm.nih.gov/pubmed/26451369
http://dx.doi.org/10.1155/2015/408495
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author Ramírez, Beatriz E.
Sánchez, Ana
Herreras, José M.
Fernández, Itziar
García-Sancho, Javier
Nieto-Miguel, Teresa
Calonge, Margarita
author_facet Ramírez, Beatriz E.
Sánchez, Ana
Herreras, José M.
Fernández, Itziar
García-Sancho, Javier
Nieto-Miguel, Teresa
Calonge, Margarita
author_sort Ramírez, Beatriz E.
collection PubMed
description Objective. To evaluate outcomes of cultivated limbal epithelial transplantation (CLET) for management of ocular surface failure due to limbal stem cell deficiency (LSCD). Design. Prospective, noncomparative, interventional case series and extensive comparison with recent similar studies. Participants. Twenty eyes with LSCD underwent CLET (11 autologous; 9 allogeneic) and were followed up for 3 years. Etiologies were divided into 3 prognostic categories: Group 1, chemical injuries (7 eyes); Group 2, immune-based inflammation (4 eyes); and Group 3, noninflammatory diseases (9 eyes). Intervention. Autologous and allogeneic limbal epithelial cells were cultivated on amniotic membranes and transplanted. Evaluations were based on clinical parameters, survival analysis, and in vivo confocal microscopy (IVCM). European Union Tissues/Cells Directive and good manufacturing procedures were followed. Main Outcome Measures. Improved clinical parameters, absence of epithelial defects, and improved central corneal epithelial phenotype. Results. Success rate was 80% at 1-2 years and 75% at 3 years. Autografts and allografts had similar survival. Success rate was significantly lower in prognostic Group 1 (42.9%) than in Groups 2-3 (100% each). All clinical parameters improved substantially. By IVCM, 80% of cases improved in epithelial status. Conclusions. CLET improved corneal epithelium quality, with subsequent improvement in symptoms, quality of life, and vision. These results confirm that CLET is a valid therapy for ocular surface failure.
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spelling pubmed-45883572015-10-08 Stem Cell Therapy for Corneal Epithelium Regeneration following Good Manufacturing and Clinical Procedures Ramírez, Beatriz E. Sánchez, Ana Herreras, José M. Fernández, Itziar García-Sancho, Javier Nieto-Miguel, Teresa Calonge, Margarita Biomed Res Int Clinical Study Objective. To evaluate outcomes of cultivated limbal epithelial transplantation (CLET) for management of ocular surface failure due to limbal stem cell deficiency (LSCD). Design. Prospective, noncomparative, interventional case series and extensive comparison with recent similar studies. Participants. Twenty eyes with LSCD underwent CLET (11 autologous; 9 allogeneic) and were followed up for 3 years. Etiologies were divided into 3 prognostic categories: Group 1, chemical injuries (7 eyes); Group 2, immune-based inflammation (4 eyes); and Group 3, noninflammatory diseases (9 eyes). Intervention. Autologous and allogeneic limbal epithelial cells were cultivated on amniotic membranes and transplanted. Evaluations were based on clinical parameters, survival analysis, and in vivo confocal microscopy (IVCM). European Union Tissues/Cells Directive and good manufacturing procedures were followed. Main Outcome Measures. Improved clinical parameters, absence of epithelial defects, and improved central corneal epithelial phenotype. Results. Success rate was 80% at 1-2 years and 75% at 3 years. Autografts and allografts had similar survival. Success rate was significantly lower in prognostic Group 1 (42.9%) than in Groups 2-3 (100% each). All clinical parameters improved substantially. By IVCM, 80% of cases improved in epithelial status. Conclusions. CLET improved corneal epithelium quality, with subsequent improvement in symptoms, quality of life, and vision. These results confirm that CLET is a valid therapy for ocular surface failure. Hindawi Publishing Corporation 2015 2015-09-16 /pmc/articles/PMC4588357/ /pubmed/26451369 http://dx.doi.org/10.1155/2015/408495 Text en Copyright © 2015 Beatriz E. Ramírez et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Study
Ramírez, Beatriz E.
Sánchez, Ana
Herreras, José M.
Fernández, Itziar
García-Sancho, Javier
Nieto-Miguel, Teresa
Calonge, Margarita
Stem Cell Therapy for Corneal Epithelium Regeneration following Good Manufacturing and Clinical Procedures
title Stem Cell Therapy for Corneal Epithelium Regeneration following Good Manufacturing and Clinical Procedures
title_full Stem Cell Therapy for Corneal Epithelium Regeneration following Good Manufacturing and Clinical Procedures
title_fullStr Stem Cell Therapy for Corneal Epithelium Regeneration following Good Manufacturing and Clinical Procedures
title_full_unstemmed Stem Cell Therapy for Corneal Epithelium Regeneration following Good Manufacturing and Clinical Procedures
title_short Stem Cell Therapy for Corneal Epithelium Regeneration following Good Manufacturing and Clinical Procedures
title_sort stem cell therapy for corneal epithelium regeneration following good manufacturing and clinical procedures
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4588357/
https://www.ncbi.nlm.nih.gov/pubmed/26451369
http://dx.doi.org/10.1155/2015/408495
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