Midterm Results of Cultivated Autologous and Allogeneic Limbal Epithelial Transplantation in Limbal Stem Cell Deficiency
Background: Limbal stem cell deficiency (LSCD) leads to growth of abnormal fibro-vascular pannus tissue onto the corneal surface as well as chronic inflammation and impaired vision. Our aim was to investigate the clinical outcome of ocular surface reconstruction in LSCD using limbal epithelial cells...
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description | Background: Limbal stem cell deficiency (LSCD) leads to growth of abnormal fibro-vascular pannus tissue onto the corneal surface as well as chronic inflammation and impaired vision. Our aim was to investigate the clinical outcome of ocular surface reconstruction in LSCD using limbal epithelial cells expanded on amniotic membrane (AM). Methods: Forty-four eyes of 38 patients (27 male, 11 female) with total (n = 32) or partial (n = 12) LSCD were treated by transplantation of autologous (n = 30) or allogeneic (n = 14) limbal epithelial cells expanded on intact AM. LSCD was caused by chemical and thermal burns (n = 22), pterygium (n = 9), congenital aniridia (n = 6), tumor excision (n = 2), perforating eye injury, mitomycin C, epidermolysis bullosa, bilateral graft-versus-host disease and chlamydial conjunctivitis (each n = 1). Results: Mean follow-up time was 28.5 ± 14.9 months. The corneal surface could be reconstructed to full stability in 30 (68%), and clear central cornea was achieved in 37 (84%) eyes. Grafting was significantly more successful in eyes treated by autologous than by allogeneic transplantation (76.7 vs. 50%, p < 0.05). The corneal surface could be successfully restored in 10 (83.3%) eyes with partial LSCD and in 20 (63.3%) eyes with total LSCD. Visual acuity (VA) increased significantly in 32 (73%) eyes, was stable in 10 (23%) eyes and decreased in 2 (4%) eyes. Mean VA increased significantly (p < 0.0001), from preoperative 1.7 ± 0.9 log MAR (20/1,000) to 0.9 ± 0.7 log-MAR (20/160). VA increased significantly after both autologous (p < 0.0001) and allogeneic transplantation (p < 0.005). Conclusions: In most patients with LSCD, transplantation of limbal epithelium cultivated on intact AM restores the corneal surface and results in significantly increased VA. |
doi_str_mv | 10.1159/000315020 |
format | Book Chapter |
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Our aim was to investigate the clinical outcome of ocular surface reconstruction in LSCD using limbal epithelial cells expanded on amniotic membrane (AM). Methods: Forty-four eyes of 38 patients (27 male, 11 female) with total (n = 32) or partial (n = 12) LSCD were treated by transplantation of autologous (n = 30) or allogeneic (n = 14) limbal epithelial cells expanded on intact AM. LSCD was caused by chemical and thermal burns (n = 22), pterygium (n = 9), congenital aniridia (n = 6), tumor excision (n = 2), perforating eye injury, mitomycin C, epidermolysis bullosa, bilateral graft-versus-host disease and chlamydial conjunctivitis (each n = 1). Results: Mean follow-up time was 28.5 ± 14.9 months. The corneal surface could be reconstructed to full stability in 30 (68%), and clear central cornea was achieved in 37 (84%) eyes. Grafting was significantly more successful in eyes treated by autologous than by allogeneic transplantation (76.7 vs. 50%, p < 0.05). The corneal surface could be successfully restored in 10 (83.3%) eyes with partial LSCD and in 20 (63.3%) eyes with total LSCD. Visual acuity (VA) increased significantly in 32 (73%) eyes, was stable in 10 (23%) eyes and decreased in 2 (4%) eyes. Mean VA increased significantly (p < 0.0001), from preoperative 1.7 ± 0.9 log MAR (20/1,000) to 0.9 ± 0.7 log-MAR (20/160). VA increased significantly after both autologous (p < 0.0001) and allogeneic transplantation (p < 0.005). Conclusions: In most patients with LSCD, transplantation of limbal epithelium cultivated on intact AM restores the corneal surface and results in significantly increased VA.</description><identifier>ISSN: 0250-3751</identifier><identifier>ISBN: 9783805594189</identifier><identifier>ISBN: 3805594186</identifier><identifier>EISSN: 1662-2790</identifier><identifier>EISBN: 9783805594196</identifier><identifier>EISBN: 3805594194</identifier><identifier>DOI: 10.1159/000315020</identifier><identifier>OCLC: 643265037</identifier><identifier>PMID: 20502027</identifier><identifier>LCCallNum: RE216.D78R47 2010</identifier><language>eng</language><publisher>Basel, Switzerland: S. Karger AG</publisher><subject>Adolescent ; Adult ; Aged ; Aged, 80 and over ; Allergies ; Amnion ; Cell Transplantation ; Cells, Cultured ; Chapter ; Child ; Cornea - physiology ; Corneal Diseases - physiopathology ; Corneal Diseases - surgery ; Epithelial Cells - transplantation ; Female ; Humans ; Limbus Corneae - cytology ; Male ; Middle Aged ; Ophthalmology ; Stem Cells - pathology ; Transplantation, Autologous ; Transplantation, Homologous ; Veterinary medicine ; Visual Acuity - physiology</subject><ispartof>Developments in ophthalmology, 2010, Vol.45, p.57-70</ispartof><rights>2010 S. Karger AG, Basel</rights><rights>Copyright 2010 S. Karger AG, Basel.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c455t-7e586fa926ac00a63805c7d0870a3390dc927c261aed28faa8d9dd0bdfa044063</citedby><relation>Research Projects in Dry Eye Syndrome</relation></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttps://ebookcentral.proquest.com/covers/3016416-l.jpg</thumbnail><link.rule.ids>775,776,780,789,26059,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20502027$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Brewitt H</contributor><contributor>Brewitt, H</contributor><creatorcontrib>Pauklin, Mikk</creatorcontrib><creatorcontrib>Fuchsluger, Thomas A.</creatorcontrib><creatorcontrib>Westekemper, Henrike</creatorcontrib><creatorcontrib>Steuhl, Klaus-P.</creatorcontrib><creatorcontrib>Meller, Daniel</creatorcontrib><title>Midterm Results of Cultivated Autologous and Allogeneic Limbal Epithelial Transplantation in Limbal Stem Cell Deficiency</title><title>Developments in ophthalmology</title><addtitle>Dev Ophthalmol</addtitle><description>Background: Limbal stem cell deficiency (LSCD) leads to growth of abnormal fibro-vascular pannus tissue onto the corneal surface as well as chronic inflammation and impaired vision. Our aim was to investigate the clinical outcome of ocular surface reconstruction in LSCD using limbal epithelial cells expanded on amniotic membrane (AM). Methods: Forty-four eyes of 38 patients (27 male, 11 female) with total (n = 32) or partial (n = 12) LSCD were treated by transplantation of autologous (n = 30) or allogeneic (n = 14) limbal epithelial cells expanded on intact AM. LSCD was caused by chemical and thermal burns (n = 22), pterygium (n = 9), congenital aniridia (n = 6), tumor excision (n = 2), perforating eye injury, mitomycin C, epidermolysis bullosa, bilateral graft-versus-host disease and chlamydial conjunctivitis (each n = 1). Results: Mean follow-up time was 28.5 ± 14.9 months. The corneal surface could be reconstructed to full stability in 30 (68%), and clear central cornea was achieved in 37 (84%) eyes. Grafting was significantly more successful in eyes treated by autologous than by allogeneic transplantation (76.7 vs. 50%, p < 0.05). The corneal surface could be successfully restored in 10 (83.3%) eyes with partial LSCD and in 20 (63.3%) eyes with total LSCD. Visual acuity (VA) increased significantly in 32 (73%) eyes, was stable in 10 (23%) eyes and decreased in 2 (4%) eyes. Mean VA increased significantly (p < 0.0001), from preoperative 1.7 ± 0.9 log MAR (20/1,000) to 0.9 ± 0.7 log-MAR (20/160). VA increased significantly after both autologous (p < 0.0001) and allogeneic transplantation (p < 0.005). Conclusions: In most patients with LSCD, transplantation of limbal epithelium cultivated on intact AM restores the corneal surface and results in significantly increased VA.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Allergies</subject><subject>Amnion</subject><subject>Cell Transplantation</subject><subject>Cells, Cultured</subject><subject>Chapter</subject><subject>Child</subject><subject>Cornea - physiology</subject><subject>Corneal Diseases - physiopathology</subject><subject>Corneal Diseases - surgery</subject><subject>Epithelial Cells - transplantation</subject><subject>Female</subject><subject>Humans</subject><subject>Limbus Corneae - cytology</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Ophthalmology</subject><subject>Stem Cells - pathology</subject><subject>Transplantation, Autologous</subject><subject>Transplantation, Homologous</subject><subject>Veterinary medicine</subject><subject>Visual Acuity - physiology</subject><issn>0250-3751</issn><issn>1662-2790</issn><isbn>9783805594189</isbn><isbn>3805594186</isbn><isbn>9783805594196</isbn><isbn>3805594194</isbn><fulltext>true</fulltext><rsrctype>book_chapter</rsrctype><creationdate>2010</creationdate><recordtype>book_chapter</recordtype><sourceid>EIF</sourceid><recordid>eNpdUcluFDEQNXtGwxz4AWROnBrKe_sYTcIiDUKCcG657erESm-03Yj8PR4mOYDqUK9Ur56qXhHyisE7xpR9DwCCKeDwiOysqUUNSlnJrH5MNkxrXnFj4ck_vdo-JRvgCiphFHtONloKrhUIc0Z2KcUWQHJhjJIvyBmHozg3G_L7SwwZl4F-w7T2OdGpo_sC4i-XMdDzNU_9dD2tibqxlH0pcMTo6SEOrevp5RzzDfaxwKvFjWnu3ZhdjtNI4_hA-p5xoHvse3qBXfQRR3_3kjzrXJ9wd5-35MeHy6v9p-rw9ePn_fmh8lKpXBlUte6c5dp5AKeP53oToDbghLAQvOXGc80cBl53ztXBhgBt6BxICVpsyduT7rxMP1dMuRli8mUXN2I5qzFCSCOgxJa8vmeu7YChmZc4uOWueTCrEPh_UthO063HMS-u9zduLk6mRgDTkulG2sYcVd-chm7dco3LaSQlXCIW6t8niz-RUZDV</recordid><startdate>20100101</startdate><enddate>20100101</enddate><creator>Pauklin, Mikk</creator><creator>Fuchsluger, Thomas A.</creator><creator>Westekemper, Henrike</creator><creator>Steuhl, Klaus-P.</creator><creator>Meller, Daniel</creator><general>S. Karger AG</general><scope>FFUUA</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>20100101</creationdate><title>Midterm Results of Cultivated Autologous and Allogeneic Limbal Epithelial Transplantation in Limbal Stem Cell Deficiency</title><author>Pauklin, Mikk ; Fuchsluger, Thomas A. ; Westekemper, Henrike ; Steuhl, Klaus-P. ; Meller, Daniel</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c455t-7e586fa926ac00a63805c7d0870a3390dc927c261aed28faa8d9dd0bdfa044063</frbrgroupid><rsrctype>book_chapters</rsrctype><prefilter>book_chapters</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Allergies</topic><topic>Amnion</topic><topic>Cell Transplantation</topic><topic>Cells, Cultured</topic><topic>Chapter</topic><topic>Child</topic><topic>Cornea - physiology</topic><topic>Corneal Diseases - physiopathology</topic><topic>Corneal Diseases - surgery</topic><topic>Epithelial Cells - transplantation</topic><topic>Female</topic><topic>Humans</topic><topic>Limbus Corneae - cytology</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Ophthalmology</topic><topic>Stem Cells - pathology</topic><topic>Transplantation, Autologous</topic><topic>Transplantation, Homologous</topic><topic>Veterinary medicine</topic><topic>Visual Acuity - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pauklin, Mikk</creatorcontrib><creatorcontrib>Fuchsluger, Thomas A.</creatorcontrib><creatorcontrib>Westekemper, Henrike</creatorcontrib><creatorcontrib>Steuhl, Klaus-P.</creatorcontrib><creatorcontrib>Meller, Daniel</creatorcontrib><collection>ProQuest Ebook Central - Book Chapters - Demo use only</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pauklin, Mikk</au><au>Fuchsluger, Thomas A.</au><au>Westekemper, Henrike</au><au>Steuhl, Klaus-P.</au><au>Meller, Daniel</au><au>Brewitt H</au><au>Brewitt, H</au><format>book</format><genre>bookitem</genre><ristype>CHAP</ristype><atitle>Midterm Results of Cultivated Autologous and Allogeneic Limbal Epithelial Transplantation in Limbal Stem Cell Deficiency</atitle><btitle>Developments in ophthalmology</btitle><addtitle>Dev Ophthalmol</addtitle><seriestitle>Research Projects in Dry Eye Syndrome</seriestitle><date>2010-01-01</date><risdate>2010</risdate><volume>45</volume><spage>57</spage><epage>70</epage><pages>57-70</pages><issn>0250-3751</issn><eissn>1662-2790</eissn><isbn>9783805594189</isbn><isbn>3805594186</isbn><eisbn>9783805594196</eisbn><eisbn>3805594194</eisbn><abstract>Background: Limbal stem cell deficiency (LSCD) leads to growth of abnormal fibro-vascular pannus tissue onto the corneal surface as well as chronic inflammation and impaired vision. Our aim was to investigate the clinical outcome of ocular surface reconstruction in LSCD using limbal epithelial cells expanded on amniotic membrane (AM). Methods: Forty-four eyes of 38 patients (27 male, 11 female) with total (n = 32) or partial (n = 12) LSCD were treated by transplantation of autologous (n = 30) or allogeneic (n = 14) limbal epithelial cells expanded on intact AM. LSCD was caused by chemical and thermal burns (n = 22), pterygium (n = 9), congenital aniridia (n = 6), tumor excision (n = 2), perforating eye injury, mitomycin C, epidermolysis bullosa, bilateral graft-versus-host disease and chlamydial conjunctivitis (each n = 1). Results: Mean follow-up time was 28.5 ± 14.9 months. The corneal surface could be reconstructed to full stability in 30 (68%), and clear central cornea was achieved in 37 (84%) eyes. Grafting was significantly more successful in eyes treated by autologous than by allogeneic transplantation (76.7 vs. 50%, p < 0.05). The corneal surface could be successfully restored in 10 (83.3%) eyes with partial LSCD and in 20 (63.3%) eyes with total LSCD. Visual acuity (VA) increased significantly in 32 (73%) eyes, was stable in 10 (23%) eyes and decreased in 2 (4%) eyes. Mean VA increased significantly (p < 0.0001), from preoperative 1.7 ± 0.9 log MAR (20/1,000) to 0.9 ± 0.7 log-MAR (20/160). VA increased significantly after both autologous (p < 0.0001) and allogeneic transplantation (p < 0.005). Conclusions: In most patients with LSCD, transplantation of limbal epithelium cultivated on intact AM restores the corneal surface and results in significantly increased VA.</abstract><cop>Basel, Switzerland</cop><pub>S. Karger AG</pub><pmid>20502027</pmid><doi>10.1159/000315020</doi><oclcid>643265037</oclcid><tpages>14</tpages></addata></record> |
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subjects | Adolescent Adult Aged Aged, 80 and over Allergies Amnion Cell Transplantation Cells, Cultured Chapter Child Cornea - physiology Corneal Diseases - physiopathology Corneal Diseases - surgery Epithelial Cells - transplantation Female Humans Limbus Corneae - cytology Male Middle Aged Ophthalmology Stem Cells - pathology Transplantation, Autologous Transplantation, Homologous Veterinary medicine Visual Acuity - physiology |
title | Midterm Results of Cultivated Autologous and Allogeneic Limbal Epithelial Transplantation in Limbal Stem Cell Deficiency |
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