Int J Immunopathol Pharmacol. 2010 Jul-Sep;23(3):701-7. doi: 10.1177/039463201002300303.
Tumor necrosis factor-alpha receptor (TNFR1)-associated periodic syndrome (TRAPS) is the most common autosomal-dominant autoinflammatory condition and is caused by mutations in the TNFRSF1A gene. TRAPS is characterized by recurrent attacks of fever typically lasting from 1 to 3 weeks; in addition to fever, common clinical features include mainly periorbital oedema, conjunctivitis, a migratory erythematous plaque simulating erysipela with underlying myalgia, and arthritis or arthralgia; serosal membrane inflammation is also possible. The identification of TNFRSF1A mutations as the genetic cause of TRAPS coincided with the wider use of biological agents in medicine and raised the possibility that blocking TNF could potentially represent the primary therapeutic goal in TRAPS, thus disclosing new treatment choices for this complex disease. In the past few years, isolated reports and case-series have been published suggesting that inhibition of TNF-alpha might represent a promising therapeutic approach in TRAPS. We present here our experience with etanercept in the treatment of patients affected with TRAPS, and we also add a review of the literature.
肿瘤坏死因子-α受体(TNFR1)相关周期性综合征(TRAPS)是最常见的常染色体显性自身炎症性疾病,由 TNFRSF1A 基因突变引起。TRAPS 的特征是反复发作的发热,通常持续 1 至 3 周;除发热外,常见的临床特征主要包括眶周水肿、结膜炎、迁移性红斑斑块,类似于伴有肌痛的丹毒,以及关节炎或关节痛;也可能发生浆膜膜炎症。TNFRSF1A 基因突变作为 TRAPS 的遗传原因的发现恰逢生物制剂在医学中的广泛应用,这提出了阻断 TNF 可能是 TRAPS 的主要治疗目标的可能性,从而为这种复杂疾病揭示了新的治疗选择。在过去几年中,已经发表了一些孤立的报告和病例系列,表明抑制 TNF-α可能是 TRAPS 的一种有前途的治疗方法。我们在此介绍我们使用依那西普治疗 TRAPS 患者的经验,并对文献进行了回顾。