Department of Ophthalmology, Graduate School of Medicine, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Ophthalmology. 2010 Dec;117(12):2247-2254.e1. doi: 10.1016/j.ophtha.2010.04.003. Epub 2010 Jul 29.
To determine the long-term epithelial lineage of origin of surgically removed grafts after allogeneic cultivated corneal limbal epithelial transplantation (CLET).
Interventional case reports.
We studied 2 eyes from 2 patients with total corneal stem cell destruction; 1 eye was from a patient with Stevens-Johnson syndrome and 1 eye had sustained chemical injury.
Allogeneic cultivated corneal limbal epithelial sheets on human amniotic membrane (AM) were transplanted onto the ocular surface. Regrafting (1 eye, 42 months later) or penetrating keratoplasty (1 eye, 75 months later) were performed after the initial transplantation procedure for further visual rehabilitation.
The excised grafts were subjected to clinical evaluation and to light- and transmission electron microscopy (TEM) examination and to immunohistochemical analysis.
In clinically conjunctival grafts, TEM and immunohistochemical analysis disclosed only small areas where the original cultivated corneal epithelial cells persisted. Neighboring conjunctival epithelial cells had apparently invaded a large portion of the corneal surface (keratin 3/12(-), Muc5ac(+)). In clinically corneal grafts, transplanted allogeneic cultivated corneal epithelial cells clearly survived for a long period of time (keratin 3/12(+), Muc5ac(-)); there was no infiltration by inflammatory cells, nor was there dissolution of the AM substrate.
We theorize that the process of graft opacification after allogeneic CLET is responsible for the loss of transplanted cultivated corneal epithelial cells and that this is followed by conjunctival cell invasion onto the corneal surface. The results of this study confirmed that in the clinically evaluated corneal graft, transplanted cultivated corneal epithelial cells indeed survived for a long period of time on the corneal surface and maintained ocular surface integrity, even though the transplanted cells were allogeneic.
确定同种异体培养角膜缘上皮移植(CLET)后手术切除移植物的长期上皮谱系起源。
干预性病例报告。
我们研究了 2 例总角膜干细胞破坏患者的 2 只眼;1 只眼来自 Stevens-Johnson 综合征患者,1 只眼持续化学损伤。
将同种异体培养的角膜缘上皮片置于人羊膜(AM)上,移植到眼表面。初次移植后进行再移植(1 只眼,42 个月后)或穿透性角膜移植(1 只眼,75 个月后),以进一步进行视力康复。
切除的移植物进行临床评估,并进行光镜和透射电镜(TEM)检查和免疫组织化学分析。
在临床上结膜移植物中,TEM 和免疫组织化学分析仅显示原始培养角膜上皮细胞持续存在的小区域。相邻的结膜上皮细胞显然已侵入大部分角膜表面(角蛋白 3/12(-),Muc5ac(+))。在临床上的角膜移植物中,移植的同种异体培养角膜上皮细胞显然存活了很长时间(角蛋白 3/12(+),Muc5ac(-));没有炎症细胞浸润,也没有 AM 基质溶解。
我们推测同种异体 CLET 后移植物混浊的过程是导致移植培养的角膜上皮细胞丢失的原因,随后是结膜细胞侵入角膜表面。本研究结果证实,在临床上评估的角膜移植物中,即使移植细胞是同种异体的,移植的培养角膜上皮细胞确实在角膜表面存活了很长时间,并维持了眼表面完整性。