Autologous serum-derived cultivated oral epithelial transplants for severe ocular surface disease

被引:73
作者
Ang, Leonard P. K.
Nakamura, Takahiro
Inatomi, Tsutomu
Sotozono, Chie
Koizumi, Noriko
Yokoi, Norihiko
Kinoshita, Shigeru [1 ]
机构
[1] Kyoto Prefectural Univ Med, Dept Ophthalmol, Kamigyo Ku, Kyoto 6020841, Japan
[2] Doshisha Univ, Res Ctr Regenerat Med, Kyoto 602, Japan
[3] Singapore Natl Eye Ctr, Singapore, Singapore
关键词
D O I
10.1001/archopht.124.11.1543
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Objective: To evaluate the use of autologous serum (AS)-derived cultivated oral epithelial transplants for the treatment of severe ocular surface disease. Methods: We used AS from 10 patients with severe ocular surface disease and total limbal stem cell deficiency to develop autologous cultivated oral epithelial equivalents. These were compared with epithelial equivalents derived from conventional fetal bovine serum supplemented medium. Surgery involved removal of the corneal pannus and surrounding diseased tissue and transplantation of the AS-derived epithelial equivalents. The oral equivalents were analyzed by review of histologic and immunohistochemical findings. Results: Oral epithelial sheets cultivated in AS- and fetal bovine serum-supplemented media were similar in morphology, and both formed basement membrane assembly proteins important for maintaining graft integrity. Complete corneal epithelialization was achieved within 2 to 5 days postoperatively. The ocular surface remained stable without major complications in all eyes during a mean +/- SD follow-up of 12.6 +/- 3.9 months. The visual acuity improved by more than 2 lines in 9 of 10 eyes, with transplanted oral epithelium surviving up to 19 months. Conclusion: The successful use of an AS-derived oral epithelial equivalent to treat severe ocular surface disease represents an important advance in the pursuit of completely autologous xenobiotic-free bioengineered ocular equivalents for clinical transplantation.
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收藏
页码:1543 / 1551
页数:9
相关论文
共 34 条
[1]   Toxic epidermal necrolysis and Stevens-Johnson syndrome are induced by soluble Fas ligand [J].
Abe, R ;
Shimizu, T ;
Shibaki, A ;
Nakamura, H ;
Watanabe, H ;
Shimizu, H .
AMERICAN JOURNAL OF PATHOLOGY, 2003, 162 (05) :1515-1520
[2]   The use of human serum in supporting the in vitro and in vivo proliferation of human conjunctival epithelial cells [J].
Ang, LPK ;
Tan, DTH ;
Seah, CJY ;
Beuerman, RW .
BRITISH JOURNAL OF OPHTHALMOLOGY, 2005, 89 (06) :748-752
[3]   THE CORNEOSCLERAL LIMBUS IN HUMAN CORNEAL EPITHELIAL WOUND-HEALING [J].
DUA, HS ;
FORRESTER, JV .
AMERICAN JOURNAL OF OPHTHALMOLOGY, 1990, 110 (06) :646-656
[4]   Desmosomes and hemidesmosomes [J].
Garrod, David R. .
CURRENT OPINION IN CELL BIOLOGY, 1993, 5 (01) :30-40
[5]   Long-term outcomes of keratolimbal allograft for the treatment of severe ocular surface disorders [J].
Ilari, L ;
Daya, SM .
OPHTHALMOLOGY, 2002, 109 (07) :1278-1284
[6]  
KENYON KR, 1989, OPHTHALMOLOGY, V96, P709
[7]  
Koizumi N, 2000, INVEST OPHTH VIS SCI, V41, P2506
[8]  
Koizumi N, 2002, INVEST OPHTH VIS SCI, V43, P2114
[9]   Amniotic membrane as a substrate for cultivating limbal corneal epithelial cells for autologous transplantation in rabbits [J].
Koizumi, N ;
Inatomi, T ;
Quantock, AJ ;
Fullwood, NJ ;
Dota, A ;
Kinoshita, S .
CORNEA, 2000, 19 (01) :65-71
[10]   Cultivated corneal epithelial stem cell transplantation in ocular surface disorders [J].
Koizumi, N ;
Inatomi, T ;
Suzuki, T ;
Sotozono, C ;
Kinoshita, S .
OPHTHALMOLOGY, 2001, 108 (09) :1569-1574