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Urea‐De‐Epithelialized Human Amniotic Membrane for Ocular Surface Reconstruction

The conjunctiva is a clear tissue covering the white part of the eye and lines the back of the eyelids. Conjunctival diseases, such as symblepharon, cause inflammation, discharges, and photophobia. The treatment often requires excision of large parts of conjunctiva. Tissue engineering of conjunctiva...

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Autores principales: Bandeira, Francisco, Yam, Gary Hin‐Fai, Fuest, Matthias, Ong, Hon Shing, Liu, Yu‐Chi, Seah, Xin‐Yi, Shen, Sunny Y., Mehta, Jodhbir S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6591546/
https://www.ncbi.nlm.nih.gov/pubmed/30868769
http://dx.doi.org/10.1002/sctm.18-0201
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author Bandeira, Francisco
Yam, Gary Hin‐Fai
Fuest, Matthias
Ong, Hon Shing
Liu, Yu‐Chi
Seah, Xin‐Yi
Shen, Sunny Y.
Mehta, Jodhbir S.
author_facet Bandeira, Francisco
Yam, Gary Hin‐Fai
Fuest, Matthias
Ong, Hon Shing
Liu, Yu‐Chi
Seah, Xin‐Yi
Shen, Sunny Y.
Mehta, Jodhbir S.
author_sort Bandeira, Francisco
collection PubMed
description The conjunctiva is a clear tissue covering the white part of the eye and lines the back of the eyelids. Conjunctival diseases, such as symblepharon, cause inflammation, discharges, and photophobia. The treatment often requires excision of large parts of conjunctiva. Tissue engineering of conjunctival cells using human amniotic membrane (HAM) denuded of its epithelium as a basement membrane scaffold has been shown to be effective for covering conjunctival defects. However, most epithelial denudation protocols are time‐consuming and expensive or compromise HAM's basement membrane structure and matrix components. We have previously described a method to de‐epithelialize HAM using ice‐cold urea (uHAM). In this report, we used this method to provide tissue‐engineered constructs with cultivated conjunctival epithelial cells on uHAM in two patients, one with a giant conjunctival nevus and the other with a large symblepharon. Autologous conjunctival epithelial cells harvested from incisional biopsies of these two patients were cultured on the uHAM scaffold. The transplantation of tissue‐engineered constructs to patients' ocular surface immediately after the removal of lesions showed successful reconstruction of the ocular surface. Postoperatively, there were neither recurrence of lesions nor epithelial defects throughout the follow‐up (up to 7 and 19 months, respectively). This report highlights the translational potential of an efficient and inexpensive method to prepare de‐epithelialized HAM as a basement membrane scaffold for cell‐based tissue‐engineered treatments of ocular surface disorders. stem cells translational medicine 2019;8:620&626
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spelling pubmed-65915462019-07-09 Urea‐De‐Epithelialized Human Amniotic Membrane for Ocular Surface Reconstruction Bandeira, Francisco Yam, Gary Hin‐Fai Fuest, Matthias Ong, Hon Shing Liu, Yu‐Chi Seah, Xin‐Yi Shen, Sunny Y. Mehta, Jodhbir S. Stem Cells Transl Med Human Clinical Article The conjunctiva is a clear tissue covering the white part of the eye and lines the back of the eyelids. Conjunctival diseases, such as symblepharon, cause inflammation, discharges, and photophobia. The treatment often requires excision of large parts of conjunctiva. Tissue engineering of conjunctival cells using human amniotic membrane (HAM) denuded of its epithelium as a basement membrane scaffold has been shown to be effective for covering conjunctival defects. However, most epithelial denudation protocols are time‐consuming and expensive or compromise HAM's basement membrane structure and matrix components. We have previously described a method to de‐epithelialize HAM using ice‐cold urea (uHAM). In this report, we used this method to provide tissue‐engineered constructs with cultivated conjunctival epithelial cells on uHAM in two patients, one with a giant conjunctival nevus and the other with a large symblepharon. Autologous conjunctival epithelial cells harvested from incisional biopsies of these two patients were cultured on the uHAM scaffold. The transplantation of tissue‐engineered constructs to patients' ocular surface immediately after the removal of lesions showed successful reconstruction of the ocular surface. Postoperatively, there were neither recurrence of lesions nor epithelial defects throughout the follow‐up (up to 7 and 19 months, respectively). This report highlights the translational potential of an efficient and inexpensive method to prepare de‐epithelialized HAM as a basement membrane scaffold for cell‐based tissue‐engineered treatments of ocular surface disorders. stem cells translational medicine 2019;8:620&626 John Wiley & Sons, Inc. 2019-03-13 /pmc/articles/PMC6591546/ /pubmed/30868769 http://dx.doi.org/10.1002/sctm.18-0201 Text en © 2019 The Authors. stem cells translational medicine published by Wiley Periodicals, Inc. on behalf of AlphaMed Press This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Human Clinical Article
Bandeira, Francisco
Yam, Gary Hin‐Fai
Fuest, Matthias
Ong, Hon Shing
Liu, Yu‐Chi
Seah, Xin‐Yi
Shen, Sunny Y.
Mehta, Jodhbir S.
Urea‐De‐Epithelialized Human Amniotic Membrane for Ocular Surface Reconstruction
title Urea‐De‐Epithelialized Human Amniotic Membrane for Ocular Surface Reconstruction
title_full Urea‐De‐Epithelialized Human Amniotic Membrane for Ocular Surface Reconstruction
title_fullStr Urea‐De‐Epithelialized Human Amniotic Membrane for Ocular Surface Reconstruction
title_full_unstemmed Urea‐De‐Epithelialized Human Amniotic Membrane for Ocular Surface Reconstruction
title_short Urea‐De‐Epithelialized Human Amniotic Membrane for Ocular Surface Reconstruction
title_sort urea‐de‐epithelialized human amniotic membrane for ocular surface reconstruction
topic Human Clinical Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6591546/
https://www.ncbi.nlm.nih.gov/pubmed/30868769
http://dx.doi.org/10.1002/sctm.18-0201
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