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角膜感染的挑战。

Challenges of corneal infections.

作者信息

Hazlett L, Suvas Susmit, McClellan Sharon, Ekanayaka Sandamali

出版信息

Expert Rev Ophthalmol. 2016;11(4):285-297. doi: 10.1080/17469899.2016.1203254. Epub 2016 Jun 30.

DOI:10.1080/17469899.2016.1203254
PMID:28090214
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5224590/
Abstract

INTRODUCTION

Ocular infections remain an important cause of blindness worldwide and represent a challenging public health concern. In this regard, microbial keratitis due to fungal, bacterial, or viral infection can result in significant vision loss secondary to corneal scarring or surface irregularity. Left untreated corneal perforation and endophthalmitis can result, leading to loss of the eye. Rigorously studied animal models of disease pathogenesis have provided novel information that suggests new modes of treatment that may be efficacious clinically and emerging clinical data is supportive of some of these discoveries.

AREAS COVERED

This review focuses on advances in our understanding of disease pathogenesis in animal models and clinical studies and how these relate to improved clinical treatment. We also discuss a novel approach to treatment of microbial keratitis due to infection with these bacterial pathogens using PACK-CXL and recommend increased basic and clinical studies to address and refine the efficacy of this procedure.

EXPERT COMMENTARY

Because resistance to antibiotics has developed over time to these bacterial pathogens, caution must be exercised in treatment. Attractive novel modes of treatment that hold new promise for further investigation include lipid based therapy, as well as use of small molecules that bind deleterious specific host responsive molecules and use of microRNA based therapies.

摘要

引言

眼部感染仍是全球失明的重要原因,是一个具有挑战性的公共卫生问题。在这方面,真菌、细菌或病毒感染引起的微生物性角膜炎可因角膜瘢痕形成或表面不规则而导致严重视力丧失。若不治疗,可导致角膜穿孔和眼内炎,进而导致失明。对疾病发病机制进行的严格动物模型研究提供了新信息,提示了可能在临床上有效的新治疗模式,并且新出现的临床数据也支持其中一些发现。

涵盖领域

本综述重点关注我们在动物模型和临床研究中对疾病发病机制的理解进展,以及这些进展与改善临床治疗的关系。我们还讨论了一种使用PACK-CXL治疗这些细菌病原体感染引起的微生物性角膜炎的新方法,并建议增加基础研究和临床研究,以探讨和完善该治疗方法的疗效。

专家评论

由于这些细菌病原体随时间推移已产生抗生素耐药性,因此在治疗时必须谨慎。具有吸引力且有望进一步研究的新治疗模式包括基于脂质的疗法,以及使用与有害的特定宿主反应性分子结合的小分子和基于微小RNA的疗法。

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Photoactivated chromophore for infectious keratitis - Corneal cross-linking (PACK-CXL): A systematic review and meta-analysis.光激活染色剂在感染性角膜炎中的应用-角膜交联术(PACK-CXL):系统评价和荟萃分析。
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Alternative Therapeutic Interventions: Antimicrobial Peptides and Small Molecules to Treat Microbial Keratitis.替代治疗干预措施:用于治疗微生物性角膜炎的抗菌肽和小分子
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本文引用的文献

1
Proteomics in the Study of Bacterial Keratitis.蛋白质组学在细菌性角膜炎研究中的应用
Proteomes. 2015 Dec 14;3(4):496-511. doi: 10.3390/proteomes3040496.
2
Use of adjunctive topical corticosteroids in bacterial keratitis.局部应用皮质类固醇辅助治疗细菌性角膜炎
Curr Opin Ophthalmol. 2016 Jul;27(4):353-7. doi: 10.1097/ICU.0000000000000273.
3
PACK-CXL: Corneal cross-linking in infectious keratitis.PACK-CXL:感染性角膜炎中的角膜交联。
Eye Vis (Lond). 2016 Apr 19;3:11. doi: 10.1186/s40662-016-0042-x. eCollection 2016.
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Inactivation of the miR-183/96/182 Cluster Decreases the Severity of Pseudomonas aeruginosa-Induced Keratitis.miR-183/96/182簇的失活降低了铜绿假单胞菌诱导的角膜炎的严重程度。
Invest Ophthalmol Vis Sci. 2016 Apr;57(4):1506-17. doi: 10.1167/iovs.16-19134.
5
Corticosteroids as a therapy for bacterial keratitis: an evidence-based review of 'who, when and why'.皮质类固醇治疗细菌性角膜炎:基于证据的“何人、何时及为何”综述
Br J Ophthalmol. 2016 Jun;100(6):731-5. doi: 10.1136/bjophthalmol-2015-307955. Epub 2016 Jan 7.
6
Thrombomodulin Protects Against Bacterial Keratitis, Is Anti-Inflammatory, but Not Angiogenic.血栓调节蛋白可预防细菌性角膜炎,具有抗炎作用,但不具有促血管生成作用。
Invest Ophthalmol Vis Sci. 2015 Dec;56(13):8091-100. doi: 10.1167/iovs.15-18393.
7
Robo 4 Counteracts Angiogenesis in Herpetic Stromal Keratitis.Robo 4抑制单纯疱疹性基质性角膜炎中的血管生成。
PLoS One. 2015 Dec 31;10(12):e0141925. doi: 10.1371/journal.pone.0141925. eCollection 2015.
8
Recent trends: Medical management of infectious keratitis.近期趋势:感染性角膜炎的医学管理
Oman J Ophthalmol. 2015 May-Aug;8(2):83-5. doi: 10.4103/0974-620X.159104.
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Lipid-Based Therapy for Ocular Surface Inflammation and Disease.眼表炎症和疾病的脂质体治疗。
Trends Mol Med. 2015 Dec;21(12):736-748. doi: 10.1016/j.molmed.2015.10.001. Epub 2015 Nov 17.
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Zinc and Manganese Chelation by Neutrophil S100A8/A9 (Calprotectin) Limits Extracellular Aspergillus fumigatus Hyphal Growth and Corneal Infection.中性粒细胞S100A8/A9(钙卫蛋白)对锌和锰的螯合作用限制了烟曲霉细胞外菌丝生长和角膜感染。
J Immunol. 2016 Jan 1;196(1):336-44. doi: 10.4049/jimmunol.1502037. Epub 2015 Nov 18.