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Gene Therapy of the Corneal Epithelium

机译:角膜上皮的基因治疗

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摘要

Despite much progress, conventional therapies have been unable to adequately treat many common disorders involving the corneal epithelium. Processes such as corneal neovascularization, conjuctivalization of the ocular surface, recurrent erosions, dry eye syndrome, and neuro-trophic keratopathy are quite frequently found to be resistant to our current treatment modalities. Our knowledge of the molecular mechanisms responsible for these disorders has flourished, but few if any of our treatments reflect our newly acquired knowledge. Most of our treatment of epithelial disease requires the repeat usage of topical drugs that are not specific for the pathophysiology of the disease to be treated, but instead effect a host of biologic processes, one of which may be involved in the pathophysiology. For many of the aforementioned disease processes, tailored molecular therapy in the form of gene therapy may prove to be more effective and harbor fewer side effects (Table 1)
机译:尽管取得了很大进展,但是常规疗法仍不能充分治疗许多涉及角膜上皮的常见疾病。诸如角膜新生血管形成,眼表结膜形成,复发性糜烂,干眼症候群和神经营养性角膜病变等过程经常被发现对我们目前的治疗方式有抵抗力。我们对导致这些疾病的分子机制的知识日渐丰富,但几乎没有一种疗法能反映出我们新获得的知识。我们上皮疾病的大多数治疗方法都需要重复使用局部药物,这些药物不是特定于待治疗疾病的病理生理学,而是会影响许多生物过程,其中一个可能与病理生理有关。对于许多上述疾病过程,以基因治疗的形式进行量身定制的分子治疗可能被证明更有效且副作用更少(表1)。

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