人表皮生长因子在穿孔角膜移植术中的泪液分泌。

German journal of ophthalmology Pub Date : 1996-09-01
S Schüller, M Knorr, K P Steuhl, H J Thiel
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引用次数: 0

摘要

人表皮生长因子(hEGF)在角膜上皮细胞再生的调控中起关键作用。由于已知泪液中EGF的浓度在角膜损伤后会降低,因此目前正在研究外源性EGF用于支持角膜伤口愈合的治疗性应用。为了评估外用EGF替代在穿孔角膜移植术中的作用,我们使用新开发的模块化免疫荧光法测定了12例患者在角膜移植术前和术后第1天和第7天的泪液中EGF的分泌。将角膜移植术患者的泪液样本中EGF的分泌和泪流率与39例其他来源的角膜上皮缺陷患者和21例健康对照者的泪液样本进行比较。与术前和健康对照(0.3 +/- 0.2 pg/s, 4.0 +/- 5.4微升/min)相比,角膜移植术患者术后样本中EGF分泌和泪液流水平(分泌0.77 +/- 0.56 pg/s,泪液流18.7 +/- 14.9微升/min)和角膜上皮缺损患者样本中EGF分泌和泪液流水平(0.6 +/- 0.4 pg/s, 19.6 +/- 19.2微升/min)反射性增加。男性的基础和反射性EGF分泌平均水平(分别为0.4和0.8 pg/s)高于女性(分别为0.25和0.55 pg/s)。结果提示,角膜刺激后泪道EGF分泌具有反射性调节的生理反馈机制。因此,重组表皮生长因子局部治疗应仅限于持续性角膜上皮缺陷和证实缺乏表皮生长因子分泌的患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Lacrimal secretion of human epidermal growth factor in perforating keratoplasty.

Human epidermal growth factor (hEGF) plays a key role in the regulation of corneal epithelial regeneration. As the lacrimal concentration of EGF is known to decrease following corneal injury, therapeutic application of exogenic EGF to support corneal wound healing is currently being investigated. To evaluate the role of topical EGF substitution in perforating keratoplasty, the lacrimal secretion of EGF was determined in 12 patients prior to keratoplasty and on the 1st and 7th days postoperatively using a newly developed modular immunofluorometric assay. EGF secretion and tear-flow rates in the tear samples of the keratoplasty patients were compared with those of 39 patients with corneal epithelial defects of other origin and those of 21 healthy controls. Levels of EGF secretion and tear flow reflectorily increased both in the post-operative samples of keratoplasty patients (secretion 0.77 +/- 0.56 pg/s, tear flow 18.7 +/- 14.9 microliter/min) and in the samples of patients with corneal epithelial defects (0.6 +/- 0.4 pg/s, 19.6 +/- 19.2 microliter/min) in comparison with preoperative values and healthy controls (0.3 +/- 0.2 pg/s, 4.0 +/- 5.4 microliter/min). Men showed higher average levels of basal and reflectory EGF secretion (0.4 and 0.8 pg/s), respectively than did women (0.25 and 0.55 pg/s, respectively). The results indicate a physiological feedback mechanism that reflectorily adjusts the lacrimal EGF secretion following corneal irritation. Topical therapy with recombinant EGF should therefore be restricted to patients with persistent corneal epithelial defects and proven deficiency of EGF secretion.

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