Autologous fibrin-cultured limbal stem cells permanently restore the corneal surface of patients with total limbal stem cell deficiency

被引:378
作者
Rama, P
Bonini, S
Lambiase, A
Golisano, O
Paterna, P
De Luca, M
Pellegrini, G
机构
[1] Ist Dermopat Immacolata, IDI, Lab Tissue Engn, I-00040 Pomezia, Roma, Italy
[2] Univ Roma Tor Vergata, Dept Ophthalmol, Rome, Italy
[3] Osped SS Giovanni & Paolo, Div Ophthalmol, Venice, Italy
关键词
D O I
10.1097/00007890-200111150-00002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Ocular burns cause depletion of limbal stem cells, which leads to corneal opacification and visual loss. Autologous cultured epithelial cells can restore damaged corneas, but this technology is still developing. We sought to establish a culture system that allows preservation of limbal stem cells and preparation of manageable epithelial sheets and to investigate whether such cultures can permanently restore total limbal stem cell deficiency. Methods. We selected a homogeneous group of patients whose limbal cell deficiency was evaluated by scoring the gravity of the clinical picture and the keratin expression pattern. Stem cells, obtained from the limbus of the contralateral eye, were cultivated onto a fibrin substrate and their preservation was evaluated by clonal analysis. Fibrin cultures were grafted onto damaged corneas. Results. Fibrin-cultured limbal stem cells were successful in 14 of 18 patients. Re-epithelialization occurred within the first week. Inflammation and vascularization regressed within the first 3-4 weeks. By the first month, the corneal surface was covered by a transparent, normal-looking epithelium. At 12-27 months follow-up, corneal surfaces were clinically and cytologically stable. Three patients had a penetrating keratoplasty approximately 1 year after restoration of their corneal surface. Their visual acuity improved from light perception or counting fingers to 0.8-1.0. Conclusions. Preservation of limbal stem cells in culture gives new perspectives on the treatment of ocular disorders characterized by complete limbal stem cell deficiency. The multicenter nature of this study and the handiness and ease of long-distance transportation of the fibrin-cultured epithelial sheets suggest that this technology can now be widely applied.
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页码:1478 / 1485
页数:8
相关论文
共 30 条
[1]   Amniotic membrane transplantation for ocular surface reconstruction [J].
Azuara-Blanco, A ;
Pillai, CT ;
Dua, HS .
BRITISH JOURNAL OF OPHTHALMOLOGY, 1999, 83 (04) :399-402
[2]   3 CLONAL TYPES OF KERATINOCYTE WITH DIFFERENT CAPACITIES FOR MULTIPLICATION [J].
BARRANDON, Y ;
GREEN, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (08) :2302-2306
[3]  
Barrandon Y., 1993, DEV BIOL, V4, P209, DOI [DOI 10.1006/SEDB.1993.1025, 10.1006/sedb.1993.1025]
[4]   EXISTENCE OF SLOW-CYCLING LIMBAL EPITHELIAL BASAL CELLS THAT CAN BE PREFERENTIALLY STIMULATED TO PROLIFERATE - IMPLICATIONS ON EPITHELIAL STEM-CELLS [J].
COTSARELIS, G ;
CHENG, SZ ;
DONG, G ;
SUN, TT ;
LAVKER, RM .
CELL, 1989, 57 (02) :201-209
[5]   Downregulation of 14-3-3σ prevents clonal evolution and leads to immortalization of primary human keratinocytes [J].
Dellambra, E ;
Golisano, O ;
Bondanza, S ;
Siviero, E ;
Lacal, P ;
Molinari, M ;
D'Atri, S ;
De Luca, M .
JOURNAL OF CELL BIOLOGY, 2000, 149 (05) :1117-1129
[6]   TREATMENT OF LEG ULCERS WITH CRYOPRESERVED ALLOGENEIC CULTURED EPITHELIUM [J].
DELUCA, M ;
ALBANESE, E ;
CANCEDDA, R ;
VIACAVA, A ;
FAGGIONI, A ;
ZAMBRUNO, G ;
GIANNETTI, A .
ARCHIVES OF DERMATOLOGY, 1992, 128 (05) :633-638
[7]   Limbal stem cells of the corneal epithelium [J].
Dua, HS ;
Azuara-Blanco, A .
SURVEY OF OPHTHALMOLOGY, 2000, 44 (05) :415-425
[8]   Stem cells: A new lease on life [J].
Fuchs, E ;
Segre, JA .
CELL, 2000, 100 (01) :143-155
[9]   PERMANENT COVERAGE OF LARGE BURN WOUNDS WITH AUTOLOGOUS CULTURED HUMAN EPITHELIUM [J].
GALLICO, GG ;
OCONNOR, NE ;
COMPTON, CC ;
KEHINDE, O ;
GREEN, H .
NEW ENGLAND JOURNAL OF MEDICINE, 1984, 311 (07) :448-451
[10]   STEM-CELL PATTERNING AND FATE IN HUMAN EPIDERMIS [J].
JONES, PH ;
HARPER, S ;
WATT, FM .
CELL, 1995, 80 (01) :83-93