Zhao Chan, Zhang Meifen
Department of Ophthalmology, Peking Medical College Hospital, Chinese Academy of Medical Sciences & Peking Medical College, Beijing 100730, China.
Chin Med Sci J. 2017 Apr 10;32(1):48-61. doi: 10.24920/j1001-9242.2007.007.
Non-infectious uveitis is one of the leading causes of preventable blindness worldwide. Long-term immunosuppressive treatment is generally required to achieve durable control of inflammation in posterior and panuveitis. Although systemic corticosteroids have been the gold standard of immunosup- pressive treatment for uveitis since first introduced in 1950s, its side effects of long-term use often warrant an adjuvant treatment to reduce the dosage/duration of corticosteroids needed to maintain disease control. Conventional immunosuppressive drugs, classified into alkylating agent, antimetabolites and T cell inhibitors, have been widely used as corticosteroid-sparing agents, each with characteristic safety/tolerance profiles on different uveitis entities. Recently, biologic agents, which target specific molecules in immunopathogenesis of uveitis, have gained great interest as alternative treatments for refractory uveitis based on their favorable safety and effectiveness in a variety of uveitis entities. However, lack of large randomized controlled clinical trials, concerns about efficacy and safety of long-term usage, and economic burden are limiting the use of biologics in non-infectious uveitis. Local administration of immunosuppressive drugs (from corticosteroids to biologics) through intraocular drug delivery systems represent another direction for drug development and is now under intense investigation, but more evidences are needed to support their use as regular alternative treatments for uveitis. With the numerous choices belonging to different treatment modalities (conventional immunosuppressive agents, biologics and local drug delivery systems) on hand, the practice patterns have been reported to vary greatly from center to center. Factors influence uveitis specialists' choices of immunosuppressive agents may be complex and may include personal familiarity, treatment availability, safety/tolerability, effectiveness, patient compliance, cost concerns and suggestions from related specialists such as rheumatologists and pediatricians. The focus of this review is to provide an overview of each treatment modality on safety/tolerability and effectiveness, which are believed to be the two most important factors affecting treatment decision making.
非感染性葡萄膜炎是全球可预防失明的主要原因之一。通常需要长期免疫抑制治疗才能持久控制后葡萄膜炎和全葡萄膜炎的炎症。自20世纪50年代首次引入以来,全身用皮质类固醇一直是葡萄膜炎免疫抑制治疗的金标准,但其长期使用的副作用常常需要辅助治疗以减少维持疾病控制所需的皮质类固醇剂量/疗程。传统免疫抑制药物分为烷化剂、抗代谢物和T细胞抑制剂,已被广泛用作皮质类固醇节约剂,每种药物在不同葡萄膜炎类型上具有独特的安全性/耐受性特征。近年来,靶向葡萄膜炎免疫发病机制中特定分子的生物制剂,因其在多种葡萄膜炎类型中具有良好的安全性和有效性,作为难治性葡萄膜炎的替代治疗方法引起了极大关注。然而,缺乏大型随机对照临床试验、对长期使用的疗效和安全性的担忧以及经济负担限制了生物制剂在非感染性葡萄膜炎中的应用。通过眼内给药系统局部应用免疫抑制药物(从皮质类固醇到生物制剂)代表了另一个药物研发方向,目前正在深入研究,但需要更多证据支持其作为葡萄膜炎常规替代治疗方法的应用。由于有多种不同治疗方式(传统免疫抑制剂、生物制剂和局部给药系统)可供选择,据报道不同中心的治疗模式差异很大。影响葡萄膜炎专家选择免疫抑制剂的因素可能很复杂,可能包括个人熟悉程度、治疗可及性、安全性/耐受性、有效性、患者依从性、成本担忧以及风湿病学家和儿科医生等相关专家的建议。本综述的重点是概述每种治疗方式在安全性/耐受性和有效性方面的情况,这两个因素被认为是影响治疗决策的最重要因素。