Oculoplastics Service, Western Eye Hospital, Imperial College Healthcare NHS Trust, London, UK.
Department of Ophthalmology, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
Eye (Lond). 2024 Jun;38(8):1425-1437. doi: 10.1038/s41433-024-02967-9. Epub 2024 Feb 19.
This review aims to provide an overview of the current understanding of TED and its pathophysiology. To describe the evidence base for current consensus treatment recommendations and newer biological therapies available as well as to present future therapeutic research.
We reviewed and assessed the peer-reviewed literature placing particular emphasis on recent studies evaluating the pathophysiology of TED, landmark trials forming the basis of current management and recent clinical trials informing future therapeutics. Searched were made in MEDLINE Ovid, Embase Ovid, US National Institutes of Health Ongoing Trials Register and EU Clinical Trials Register. Keywords included: "Thyroid Eye Disease", "Graves Orbitopathy", "Thyroid Orbitopathy" and "Graves' Ophthalmopathy".
The pathophysiology of TED involves a complex array of cellular and humoral based autoimmune dysfunction. Previous therapies have been broad-based acting as a blunt instrument on this mechanism with varying efficacy but often accompanied with a significant side effect profile. The recent development of targeted therapy, spearheaded by Teprotumumab has led to an array of treatments focusing on specific components of the molecular pathway optimising their impact whilst possibly minimising their side effect profile. Future challenges involve identifying the most effective target for each patient rather than any single agent being a panacea. Long-term safety profiles will require clarification as unintended immunological consequence downstream may become manifest as seen in other diseases. Finally, future novel therapeutics will entail significant expenditure and may lead to a divergence of available treatment modalities between healthcare systems due to funding disparities.
本综述旨在概述 TED 的现有认识及其病理生理学。描述当前共识治疗建议的证据基础以及新的生物疗法,并介绍未来的治疗研究。
我们对同行评议文献进行了审查和评估,特别强调了最近评估 TED 病理生理学的研究、构成当前管理基础的标志性试验以及为未来治疗提供信息的最近临床试验。在 MEDLINE Ovid、Embase Ovid、美国国立卫生研究院正在进行的试验登记处和欧盟临床试验登记处进行了检索。关键词包括:“甲状腺眼病”、“格雷夫斯眼病”、“甲状腺眼病”和“格雷夫斯眶病”。
TED 的病理生理学涉及一系列复杂的基于细胞和体液的自身免疫功能障碍。以前的治疗方法是广泛的,作为对这种机制的一种钝器,疗效不一,但通常伴随着明显的副作用。最近靶向治疗的发展,以 Teprotumumab 为先导,已经产生了一系列针对分子途径特定成分的治疗方法,优化了它们的影响,同时可能最小化其副作用谱。未来的挑战包括为每个患者确定最有效的靶点,而不是任何单一药物都是万灵药。长期安全性概况需要澄清,因为下游的意外免疫后果可能会在其他疾病中显现出来。最后,未来的新型治疗方法将需要大量支出,并且由于资金差异,可能导致医疗保健系统之间可用治疗方式的分歧。