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眼部过敏的免疫发病机制:针对不同临床实体的示意图方法

Immunopathogenesis of ocular allergy: a schematic approach to different clinical entities.

作者信息

Leonardi Andrea, De Dominicis Chiara, Motterle Laura

机构信息

Ophthalmology Unit, Department of Neuroscience, University of Padua, Italy.

出版信息

Curr Opin Allergy Clin Immunol. 2007 Oct;7(5):429-35. doi: 10.1097/ACI.0b013e3282ef8674.

Abstract

PURPOSE OF REVIEW

The immunopathogenesis of ocular allergic disorders is generally related to the specific immunoglobulin E-mediated mast cell activation and the following cascade of inflammatory mediators. Seasonal and perennial allergic conjunctivitis, however, are the only ocular diseases to involve solely type I hypersensitivity. The other main forms, vernal and atopic keratoconjunctivitis, have a more complex immunological basis and a chronic inflammatory component. Involvement of inflammatory cells, particularly eosinophils and T cells, cytokines and proteases can lead to more serious corneal damage with vision-threatening potential.

RECENT FINDINGS

Experimental allergic conjunctival models and clinical research studies have shown that T helper type 2-related mechanisms are definitely involved in the sensitization phase of ocular allergy, however, both T helper type 1 and type 2 cytokines are overexpressed in the active disease, contributing to the development of ocular inflammation.

SUMMARY

A review of the recent literature allows us to better understand the mechanisms involved in the development of ocular allergy and to guide us toward a more schematic approach, which could possibly be useful in forming a new classification, standardizing clinical phases and individuating new treatment targets.

摘要

综述目的

眼部过敏性疾病的免疫发病机制通常与特异性免疫球蛋白E介导的肥大细胞活化以及随后的一系列炎症介质有关。然而,季节性和常年性过敏性结膜炎是仅涉及I型超敏反应的眼部疾病。其他主要形式,如春季角结膜炎和特应性角结膜炎,具有更复杂的免疫学基础和慢性炎症成分。炎症细胞,特别是嗜酸性粒细胞和T细胞、细胞因子和蛋白酶的参与可导致更严重的角膜损伤,具有威胁视力的潜在风险。

最新发现

实验性过敏性结膜模型和临床研究表明,2型辅助性T细胞相关机制肯定参与眼部过敏的致敏阶段,然而,1型和2型辅助性T细胞细胞因子在活动性疾病中均过度表达,促进眼部炎症的发展。

总结

对近期文献的综述使我们能够更好地理解眼部过敏发生发展的机制,并指导我们采用更具系统性的方法,这可能有助于形成新的分类、规范临床阶段并确定新的治疗靶点。

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