Bartakova Alena, Kunzevitzky Noelia J, Goldberg Jeffrey L
Shiley Eye Center, University of California San Diego, La Jolla, CA 92093.
Shiley Eye Center, University of California San Diego, La Jolla, CA 92093 ; Emmetrope Ophthalmics, Key Biscayne, FL 33149.
Curr Ophthalmol Rep. 2014 Sep 1;2(3):81-90. doi: 10.1007/s40135-014-0043-7.
Endothelial cell dysfunction as in Fuchs dystrophy or pseudophakic bullous keratopathy, and the limited regenerative capacity of human corneal endothelial cells (HCECs), drive the need for corneal transplant. In response to limited donor corneal availability, significant effort has been directed towards cell therapy as an alternative to surgery. Stimulation of endogenous progenitors, or transplant of stem cell-derived HCECs or -expanded, donor-derived HCECs could replace traditional surgery with regenerative therapy. expansion of HCECs is technically challenging, and the basis for molecular identification of functional HCECs is not established. Delivery of cells to the inner layer of the human cornea is another challenge: different techniques, from simple injection to artificial corneal scaffolds, are being investigated. Despite remaining questions, corneal endothelial cell therapies, translated to the clinic, represent the future for the treatment of corneal endotheliopathies.
在富克斯营养不良或人工晶状体性大疱性角膜病变中出现的内皮细胞功能障碍,以及人角膜内皮细胞(HCEC)有限的再生能力,促使人们需要进行角膜移植。由于供体角膜供应有限,人们付出了巨大努力将细胞疗法作为手术的替代方法。刺激内源性祖细胞,或移植干细胞衍生的HCEC或扩增的供体来源的HCEC,可以用再生疗法取代传统手术。HCEC的扩增在技术上具有挑战性,并且尚未建立功能性HCEC分子鉴定的基础。将细胞输送到人类角膜内层是另一个挑战:正在研究从简单注射到人工角膜支架等不同技术。尽管仍有问题,但转化为临床应用的角膜内皮细胞疗法代表了角膜内皮病变治疗的未来。