Cordeiro M Francesca
Department of Pathology, Moorfields Eye Hospital and Institute of Ophthalmology, Bath Street, London EC1V 9EL, UK.
Clin Sci (Lond). 2003 Feb;104(2):181-7. doi: 10.1042/CS20020150.
Glaucoma is the major cause of irreversible blindness throughout the world. Of all of the treatments that are available at present, the most effective appears to be surgery; however, excessive conjunctival scarring can lead to surgical failure. In the last decade, the introduction of the anti-metabolites mitomycin-C and 5-fluorouracil as anti-scarring treatments have greatly improved the results of glaucoma surgery, but these agents are associated with complications that can potentially result in blindness. A possible target for a more physiological approach to anti-scarring is transforming growth factor beta. This review examines the role of transforming growth factor beta in conjunctival scarring and discusses promising new ways of modifying its activity.
青光眼是全球不可逆性失明的主要原因。在目前所有可用的治疗方法中,最有效的似乎是手术;然而,过度的结膜瘢痕形成可导致手术失败。在过去十年中,抗代谢药物丝裂霉素-C和5-氟尿嘧啶作为抗瘢痕治疗药物的引入,极大地改善了青光眼手术的效果,但这些药物与可能导致失明的并发症有关。一种更符合生理的抗瘢痕方法的可能靶点是转化生长因子β。本文综述了转化生长因子β在结膜瘢痕形成中的作用,并讨论了调节其活性的有前景的新方法。