Graves 病和甲状腺相关眼病的靶向生物治疗。重点介绍利妥昔单抗对 B 细胞的耗竭作用。
Targeted biological therapies for Graves' disease and thyroid-associated ophthalmopathy. Focus on B-cell depletion with Rituximab.
机构信息
Department of Endocrinology and Metabolism, Odense University Hospital, University of Southern Denmark, Denmark.
出版信息
Clin Endocrinol (Oxf). 2011 Jan;74(1):1-8. doi: 10.1111/j.1365-2265.2010.03806.x.
Based on experience from the treatment of other autoimmune diseases and because of the limitations imposed by existing therapeutic options for Graves' disease (GD) and thyroid-associated ophthalmopathy (TAO), rituximab (RTX) was recently proposed as a novel therapy option. Here, we summarize the rationale for using RTX; give an overview of the possible mechanisms of action; and give an account of its effects and side-effects when used in GD and TAO. Scant evidence, originating from only a few methodologically inhomogeneous studies, suggests that RTX may prolong remission for hyperthyroidism over that seen with antithyroid drugs, at least in mild GD. Furthermore, in patients with TAO, who are unresponsive to conventional immunosuppressive therapy, RTX seems efficacious. As we wait for larger-scale randomized studies, RTX, should be considered experimental and reserved for patients who do not respond favourably to conventional therapy. It is the first in what is likely to be a series of new and emerging treatments specifically targeting relevant components of the immune system. Further studies will hopefully lead to improved and better tailored, individualized therapy for GD and especially TAO.
基于治疗其他自身免疫性疾病的经验,并且由于 Graves 病(GD)和甲状腺相关眼病(TAO)的现有治疗选择所带来的限制,利妥昔单抗(RTX)最近被提议作为一种新的治疗选择。在这里,我们总结了使用 RTX 的基本原理;概述了可能的作用机制;并说明了它在 GD 和 TAO 中的作用和副作用。只有少数几项方法学上不均匀的研究提供的证据表明,RTX 可能会延长甲状腺功能亢进症的缓解期,而不是抗甲状腺药物所看到的缓解期,至少在轻度 GD 中是这样。此外,对于对常规免疫抑制治疗无反应的 TAO 患者,RTX 似乎有效。在我们等待更大规模的随机研究的同时,RTX 应被视为实验性治疗,仅保留给那些对常规治疗反应不佳的患者。它是第一个可能针对免疫系统相关成分的一系列新的和新兴治疗方法中的第一个。进一步的研究有望为 GD 特别是 TAO 带来更好和更有针对性的个体化治疗。