Tabibian David, Richoz Olivier, Hafezi Farhad
Laboratory for Ocular Cell Biology, Faculty of Medicine, University of Geneva, Geneva, Switzerland.
Laboratory for Ocular Cell Biology, Faculty of Medicine, University of Geneva, Geneva, Switzerland ; Department of Ophthalmology, University of Southern California, Los Angeles, California, USA ; The ELZA Institute, Dietikon/Zurich, Switzerland.
J Ophthalmic Vis Res. 2015 Jan-Mar;10(1):77-80. doi: 10.4103/2008-322X.156122.
This article discusses corneal cross-linking (CXL) and how it transitioned from a modality for treating corneal ectatic disorders to an inventive means of treating infectious keratitis. Initially, CXL was successfully developed to halt the progression of ectatic diseases such as keratoconus, using the standard Dresden protocol. Later, indications were extended to treat iatrogenic ectasia developing after laser-assisted in situ keratomileusis (LASIK) and photo-refractive keratectomy (PRK). At the time, it had been postulated that the combination of ultraviolet light with riboflavin could not only biomechanically strengthen the cornea but also was capable of destroying living cells and organisms including keratocytes and pathogens. Thus a new and innovative concept of treatment for infectious keratitis emerged through the use of CXL technology. Initially only advanced infectious melting ulcers resisting standard microbicidal therapy were treated with CXL in addition to standard therapy. In subsequent studies CXL was also used to treat bacterial keratitis as first line therapy without the use of concomitant antibiotic therapy. With the increasing interest in CXL technology to treat infectious keratitis and to clearly separate its use from the treatment of ectatic disorders, a new term was adopted at the 9(th) CXL congress in Dublin for this specific indication: PACK-CXL (photoactivated chromophore for infectious keratitis). PACK-CXL has the potential to eventually become an interesting alternative to standard antibiotic therapy in treating infectious corneal disorders, and may help reduce the global burden of microbial resistance to antibiotics and other therapeutic agents.
本文讨论了角膜交联术(CXL)及其如何从一种治疗角膜扩张性疾病的方法转变为一种治疗感染性角膜炎的创新手段。最初,CXL通过使用标准的德累斯顿方案成功开发出来,用于阻止圆锥角膜等扩张性疾病的进展。后来,其适应症扩展到治疗激光原位角膜磨镶术(LASIK)和准分子激光角膜切削术(PRK)后发生的医源性角膜扩张。当时,有人推测紫外线与核黄素的结合不仅可以在生物力学上强化角膜,还能够破坏包括角膜细胞和病原体在内的活细胞和生物体。因此,通过使用CXL技术,出现了一种治疗感染性角膜炎的全新创新概念。最初,只有那些抵抗标准杀菌治疗的晚期感染性溃疡性角膜溃疡,在标准治疗的基础上联合CXL进行治疗。在随后的研究中,CXL也被用作细菌性角膜炎的一线治疗方法,而不使用联合抗生素治疗。随着对CXL技术治疗感染性角膜炎的兴趣日益增加,并且为了将其使用与角膜扩张性疾病的治疗明确区分开来,在都柏林举行的第9届CXL大会上,针对这一特定适应症采用了一个新术语:PACK-CXL(用于感染性角膜炎的光活化发色团)。PACK-CXL有可能最终成为治疗感染性角膜疾病的一种有趣的替代标准抗生素治疗的方法,并可能有助于减轻全球微生物对抗生素和其他治疗药物耐药性的负担。