Chair of Experimental Bioinformatics, Technical University of Munich, Munich, Germany.
La Jolla Institute for Immunology, La Jolla, CA, United States.
Front Immunol. 2020 Sep 29;11:1930. doi: 10.3389/fimmu.2020.01930. eCollection 2020.
Dry eye disease (DED) can be represented as a display of disease in the mucosal part of the eye. It is quite distinct from the retinal side of the eye which connects with the neurons and thus represents the neuroimmunological disease. DED can occur either by the internal damage of the T cells inside the body or by microbial infections. Here we summarize the most common animal model systems used for DED relating to immune factors. We aimed to identify the most important immune cell/cytokine among the animal models of the disease. We also show the essential immune factors which are being tested for DED treatment. In our results, both the mechanism and the treatment of its animal models indicate the involvement of Th1 cells and the pro-inflammatory cytokine (IL-1β and TNF-α) related to the Th1-cells. The study is intended to increase the knowledge of the animal models in the field of the ocular surface along with the opening of a dimension of thoughts while designing a new animal model or treatment paradigm for ocular surface inflammatory disorders.
干眼症(DED)可表现为眼部黏膜部位的疾病。它与连接神经元的视网膜侧截然不同,代表着神经免疫性疾病。DED 可由体内 T 细胞的内部损伤或微生物感染引起。在这里,我们总结了与免疫因素有关的 DED 最常见的动物模型系统。我们旨在确定疾病动物模型中最重要的免疫细胞/细胞因子。我们还展示了正在测试用于 DED 治疗的重要免疫因素。在我们的结果中,疾病动物模型的机制和治疗均表明 Th1 细胞及其相关的促炎细胞因子(IL-1β 和 TNF-α)的参与。本研究旨在增加人们对眼部表面领域动物模型的了解,并在设计新的眼部表面炎症性疾病动物模型或治疗方案时开拓思路。