Ophthalmic Biophysics Center, Bascom Palmer Eye Institute, University of Miami Miller School of Medicine, 1638 NW 10 Avenue, Miami, FL 33136, USA.
Graefes Arch Clin Exp Ophthalmol. 2011 Feb;249(2):253-60. doi: 10.1007/s00417-010-1497-4. Epub 2010 Sep 3.
To evaluate the long-term clinical and immunohistological outcome of two different non-penetrating keratoprosthesis (KPro) implanted in non-injured rabbit corneas.
Three rabbits underwent implantation of a pHEMA-MMA(34) synthetic cornea in the supradescemetic space, and PMMA synthetic corneas in the supradescemetic space and within the central stroma. Animals were followed for at least 24 months before euthanasia. Periodic evaluation was performed with slit-lamp examination and photography. At the end of the follow-up, histological examination including hematoxylin eosin staining and immunocharacterization against collagen IV, alpha smooth muscle actin (α-SMA) and macrophages was performed.
The pHEMA-MMA(34) implant was not extruded, and remained transparent until the end of follow-up. This material did not induce any cell infiltration, corneal scarring or tissue remodeling in the surrounding stroma as shown by immunofluorescence. In contrast, synthetic corneas made of PMMA-induced myofibroblast differentiation, stromal remodeling and macrophage infiltration. This reaction was even more significant in the rabbit with the PMMA implant within the corneal stroma.
pHEMA-MMA(34) was clinically biocompatible, and did not induce any inflammatory reaction or scarring when implanted in the supradescemetic space. This material showed more promising biocompatibility results than for PMMA, whether implanted within the central cornea stroma or in the supradescemetic space.
评估两种不同的非穿透性角膜假体(KPro)在未受伤兔角膜中植入的长期临床和免疫组织学结果。
三只兔子的上方巩膜空间内植入了 pHEMA-MMA(34) 合成角膜,中央基质内植入了 PMMA 合成角膜。在安乐死之前,至少随访 24 个月。通过裂隙灯检查和摄影进行定期评估。在随访结束时,进行组织学检查,包括苏木精-伊红染色以及针对胶原 IV、α 平滑肌肌动蛋白(α-SMA)和巨噬细胞的免疫特征化。
pHEMA-MMA(34) 植入物未被挤出,并且在随访结束时仍保持透明。该材料未引起任何细胞浸润、角膜瘢痕或周围基质的组织重塑,免疫荧光显示。相比之下,由 PMMA 制成的合成角膜诱导了肌成纤维细胞分化、基质重塑和巨噬细胞浸润。在 PMMA 植入角膜基质内的兔子中,这种反应更为明显。
pHEMA-MMA(34)在上方巩膜空间内植入时具有临床生物相容性,不会引起任何炎症反应或瘢痕形成。与 PMMA 相比,这种材料在中央角膜基质内或上方巩膜空间内植入时表现出更有前途的生物相容性结果。