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干眼综合征

Dry eye syndromes.

作者信息

Barabino Stefano, Dana M Reza

机构信息

Laboratory of Immunology, Schepens Eye Research Institute, and Cornea Service, Massachusetts Eye and Ear Infirmary, Department of Ophthalmology, Harvard Medical School, Boston, Mass., USA.

出版信息

Chem Immunol Allergy. 2007;92:176-184. doi: 10.1159/000099268.

Abstract

Over the past 20 years it has become clear that dry eye syndrome (DES) or keratoconjunctivitis sicca (KCS) is a complex multifactorial disease characterized by an immune and inflammatory process that affects the lacrimal glands and ocular surface. In this paradigm, inflammation is seen as both the cause and consequence of conjunctival and corneal cell damage. In this chapter, we identify the unique characteristics of the lacrimal gland, the role of epithelial cells, regulatory T cells, and cytokines in maintaining ocular surface homeostasis and tear secretion function. We analyze the factors inducing loss of the lacrimal gland homeostasis and its consequences, and in so doing hope to provide a picture of the role of the immune system in the pathophysiology of KCS and useful information to help understand the complexity of DES.

摘要

在过去20年里,很明显干眼综合征(DES)或角结膜干燥症(KCS)是一种复杂的多因素疾病,其特征是影响泪腺和眼表的免疫和炎症过程。在这种模式下,炎症被视为结膜和角膜细胞损伤的原因和结果。在本章中,我们确定了泪腺的独特特征、上皮细胞、调节性T细胞和细胞因子在维持眼表稳态和泪液分泌功能中的作用。我们分析了导致泪腺稳态丧失的因素及其后果,希望借此描绘免疫系统在KCS病理生理学中的作用,并提供有用信息,以帮助理解DES的复杂性。

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