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甲状腺相关性眼病药物治疗的新观点

Novel perspectives on the pharmacological treatment of thyroid-associated ophthalmopathy.

作者信息

Li Zilin

机构信息

No. 1 Teaching Hospital, Norman Bethune College of Medicine, Jilin University, Changchun, Jilin, China.

出版信息

Front Endocrinol (Lausanne). 2025 Jan 13;15:1469268. doi: 10.3389/fendo.2024.1469268. eCollection 2024.

DOI:10.3389/fendo.2024.1469268
PMID:39872310
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11769798/
Abstract

Thyroid-associated ophthalmopathy (TAO), an autoimmune disease closely related to thyroid dysfunction, remains a challenging ophthalmic condition among adults. Its clinical manifestations are complex and diverse, and disease progression can lead to exophthalmos, diplopia, exposure keratitis, corneal ulceration, and compressive optic neuropathy, resulting in irreversible vision damage or even blindness. Traditional treatment methods for TAO, including glucocorticoids, immunosuppressants, and radiation therapy, often have limitations and side effects, making this disease problematic in ophthalmology. As a result, the development of novel targeted drugs has become a research hotspot for addressing the pathogenesis of TAO. A range of novel targeted drugs, such as teprotumumab and tocilizumab, have been successfully developed and demonstrated remarkable efficacy in relieving inflammation and managing this disease. In addition, some drug candidates and molecular targets identified in the TAO model have shown promising prospects. This article briefly reviews the potential new strategies for future clinical treatment and the progress of new drug therapies for TAO.

摘要

甲状腺相关性眼病(TAO)是一种与甲状腺功能障碍密切相关的自身免疫性疾病,在成年人中仍然是一种具有挑战性的眼科疾病。其临床表现复杂多样,疾病进展可导致眼球突出、复视、暴露性角膜炎、角膜溃疡和压迫性视神经病变,从而导致不可逆的视力损害甚至失明。TAO的传统治疗方法,包括糖皮质激素、免疫抑制剂和放射治疗,往往存在局限性和副作用,使得这种疾病在眼科领域成为难题。因此,开发新型靶向药物已成为解决TAO发病机制的研究热点。一系列新型靶向药物,如替普罗单抗和托珠单抗,已成功研发并在减轻炎症和治疗该疾病方面显示出显著疗效。此外,在TAO模型中确定的一些候选药物和分子靶点也显示出了有前景的前景。本文简要综述了TAO未来临床治疗的潜在新策略和新药治疗的进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8b7/11769798/962c0570905c/fendo-15-1469268-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8b7/11769798/2e1e45a1280f/fendo-15-1469268-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8b7/11769798/962c0570905c/fendo-15-1469268-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8b7/11769798/2e1e45a1280f/fendo-15-1469268-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d8b7/11769798/962c0570905c/fendo-15-1469268-g002.jpg

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Exp Eye Res. 2024 Mar;240:109812. doi: 10.1016/j.exer.2024.109812. Epub 2024 Feb 9.
2
TMEM2 inhibits the development of Graves' orbitopathy through the JAK-STAT signaling pathway.TMEM2 通过 JAK-STAT 信号通路抑制格雷夫斯眼病的发展。
J Biol Chem. 2024 Feb;300(2):105607. doi: 10.1016/j.jbc.2023.105607. Epub 2023 Dec 28.
3
Crocin Inhibits Orbital Fibroblasts Fibrosis in Thyroid-Associated Ophthalmopathy.
藏红花素抑制甲状腺相关眼病眼眶成纤维细胞纤维化。
Curr Eye Res. 2024 Mar;49(3):330-337. doi: 10.1080/02713683.2023.2280441. Epub 2023 Nov 20.
4
Efficacy and Safety of Teprotumumab in Patients With Thyroid Eye Disease of Long Duration and Low Disease Activity.特罗特单抗治疗长病程和低疾病活动度甲状腺眼病患者的疗效和安全性。
J Clin Endocrinol Metab. 2023 Dec 21;109(1):25-35. doi: 10.1210/clinem/dgad637.
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Yes-Associated Protein Mediates the Transition from Inflammation to Fibrosis in Graves' Orbitopathy.Yes相关蛋白介导Graves眼病中从炎症到纤维化的转变。
Thyroid. 2023 Dec;33(12):1465-1475. doi: 10.1089/thy.2023.0309. Epub 2023 Nov 15.
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Linsitinib, an IGF-1R inhibitor, attenuates disease development and progression in a model of thyroid eye disease.林西替尼,一种 IGF-1R 抑制剂,可减轻甲状腺眼病模型中的疾病发展和进展。
Front Endocrinol (Lausanne). 2023 Jun 26;14:1211473. doi: 10.3389/fendo.2023.1211473. eCollection 2023.
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Front Endocrinol (Lausanne). 2023 Jun 22;14:1186105. doi: 10.3389/fendo.2023.1186105. eCollection 2023.
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