Chen Peng, Zhou Qingjun, Wang Junyi, Zhao Xiaowen, Duan Haoyun, Wang Yao, Liu Ting, Xie Lixin
Shandong Academy of Medical Sciences, Shandong Eye Institute, 5 Yan'erdao Road, Qingdao, 266071, China.
Graefes Arch Clin Exp Ophthalmol. 2016 Sep;254(9):1765-77. doi: 10.1007/s00417-016-3410-2. Epub 2016 Jun 16.
The objective of this study was to characterize the changes that occur in the cornea during Limbal Stem Cell Deficiency (LSCD) and on the corneal surface after transplantation of ex vivo cultured allogeneic limbal epithelial transplantation (CALET).
Forty-one pannus were analyzed to characterize the changes found in the cornea in LSCD. Nineteen impression cytology samples, including 14 pannus and five corneal buttons, obtained during subsequent procedures from patients who had undergone CALET were examined to assess the effect of CALET and to determine the long-term fate of donor cells. The presence of donor and recipient epithelial cells in each sample was determined by short tandem repeat (STR) amplification and fluorescent-multiplex polymerase chain reaction (PCR). Phenotypic analysis of the epithelium was performed by immunohistochemistry and real-time PCR.
The expression of lineage markers was similar between pannus and conjunctivae, but not to corneas. Objective long-term benefits from the transplantation were recorded in most cases. After CALET, the lineage markers in the excised corneal buttons and pannus showed a limbus phenotype. DNA analysis of the 19 cases showed no donor cells present on the ocular surface beyond three months after CALET.
LSCD was characterized by ingrowth of abnormal, inflamed tissue with a conjunctival phenotype. CALET was a useful technique for restoring the ocular surface in LSCD. However, such benefits did not necessarily correlate with survival of measurable numbers of donor cells on the ocular surface. The absence of donor DNA beyond three months raises questions regarding the period of ongoing immunosuppression and the origin of the regenerated corneal epithelium.
本研究的目的是描述角膜缘干细胞缺乏(LSCD)期间角膜发生的变化,以及体外培养的同种异体角膜缘上皮移植(CALET)后角膜表面的变化。
分析41个血管翳,以描述LSCD角膜中发现的变化。检查了19个印迹细胞学样本,包括14个血管翳和5个角膜植片,这些样本是在随后的手术中从接受CALET的患者身上获得的,以评估CALET的效果并确定供体细胞的长期命运。通过短串联重复序列(STR)扩增和荧光多重聚合酶链反应(PCR)确定每个样本中供体和受体上皮细胞的存在。通过免疫组织化学和实时PCR对上皮进行表型分析。
血管翳和结膜之间谱系标志物的表达相似,但与角膜不同。大多数病例记录了移植带来的客观长期益处。CALET后,切除的角膜植片和血管翳中的谱系标志物显示出角膜缘表型。对19例病例的DNA分析显示,CALET后三个月以上眼表未发现供体细胞。
LSCD的特征是具有结膜表型的异常炎症组织向内生长。CALET是恢复LSCD眼表的一种有用技术。然而,这些益处不一定与眼表可测量数量的供体细胞存活相关。三个月后供体DNA的缺失引发了关于持续免疫抑制期和再生角膜上皮来源的问题。