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用于研究甲状腺相关性眼病的动物模型的建立与应用

Development and application of animal models to study thyroid-associated ophthalmopathy.

作者信息

Shen Feiyang, Liu Jin, Fang Lianfei, Fang Yan, Zhou Huifang

机构信息

Department of Ophthalmology, Ninth People's Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, 200025, China; Shanghai Key Laboratory of Orbital Diseases and Ocular Oncology, Shanghai, 200025, China.

Department of Ophthalmology, Ninth People's Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, 200025, China; Shanghai Key Laboratory of Orbital Diseases and Ocular Oncology, Shanghai, 200025, China.

出版信息

Exp Eye Res. 2023 May;230:109436. doi: 10.1016/j.exer.2023.109436. Epub 2023 Mar 11.

Abstract

Thyroid-associated ophthalmopathy (TAO), also known as Graves' ophthalmopathy, is an autoimmune disease that is usually accompanied by hyperthyroidism. Its pathogenesis involves the activation of autoimmune T lymphocytes by a cross-antigen reaction of thyroid and orbital tissues. The thyroid-stimulating hormone receptor (TSHR) is known to play an important role in the development of TAO. Because of the difficulty of orbital tissue biopsy, the establishment of an ideal animal model is important for developing novel clinical therapies of TAO. To date, TAO animal modeling methods are mainly based on inducing experimental animals to produce anti-thyroid-stimulating hormone receptor antibodies (TRAbs) and then recruit autoimmune T lymphocytes. Currently, the most common methods are hTSHR-A subunit plasmid electroporation and hTSHR-A subunit adenovirus transfection. These animal models provide a powerful tool for exploring the internal relationship between local and systemic immune microenvironment disorders of the TAO orbit, facilitating the development of new drugs. However, existing TAO modeling methods still have some defects, such as low modeling rate, long modeling cycles, low repetition rate, and considerable differences from human histology. Hence, the modeling methods require further innovation, improvement, and in-depth exploration.

摘要

甲状腺相关眼病(TAO),也称为格雷夫斯眼病,是一种通常伴有甲状腺功能亢进的自身免疫性疾病。其发病机制涉及甲状腺和眼眶组织的交叉抗原反应激活自身免疫性T淋巴细胞。已知促甲状腺激素受体(TSHR)在TAO的发展中起重要作用。由于眼眶组织活检困难,建立理想的动物模型对于开发TAO的新型临床治疗方法很重要。迄今为止,TAO动物建模方法主要基于诱导实验动物产生抗促甲状腺激素受体抗体(TRAbs),然后募集自身免疫性T淋巴细胞。目前,最常用的方法是hTSHR - A亚基质粒电穿孔和hTSHR - A亚基腺病毒转染。这些动物模型为探索TAO眼眶局部和全身免疫微环境紊乱之间的内在关系提供了有力工具,促进了新药的开发。然而,现有的TAO建模方法仍然存在一些缺陷,如建模率低、建模周期长、重复率低以及与人类组织学有相当大的差异。因此,建模方法需要进一步创新、改进和深入探索。

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