Laboratory of Parasitic Diseases, National Institutes of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland.
Department of Medicine, Albert Einstein College of Medicine, Bronx, New York.
Am J Trop Med Hyg. 2019 Mar;100(3):609-616. doi: 10.4269/ajtmh.18-0795.
Manifestations of neurocysticercosis (NCC) are primarily due to host inflammatory responses directed at drug-damaged or naturally degenerating metacestodes (cysts) of the tapeworm . Prolonged high-dose corticosteroids are frequently required to control this inflammation in complicated disease, often causing severe side effects. Studies evaluating alternatives to corticosteroids are lacking. Here, we describe the clinical course of NCC in 16 patients prescribed etanercept (ETN), a tumor necrosis factor-alpha inhibitor to control inflammation resulting from anthelmintic treatment. Twelve patients with extraparenchymal NCC were administered ETN with corticosteroids (11/12, 91.7%) and/or methotrexate (9/12, 75.0%). The median age of the subgroup with extraparenchymal NCC was 40 years (range 26-57 years) and 66.7% were male. They were administered ETN for a median period of 311 days (range 31-461 days) and then followed for a median of 3.4 years (range 0.3-6.6 years). Among nine assessable patients, all improved clinically after starting ETN and one deteriorated transiently. Of the remaining three, one was lost to follow-up and two patients have improved but had not completed their assigned course. Four additional persons with recurrent perilesional edema (PE) episodes were given ETN for a median of 400.5 days (range 366-854 days) and followed post-ETN for a median of 1.7 years (range 0.2-2.4 years). All PE patients improved and two successfully tapered corticosteroids. Etanercept administration was associated with clinical improvement, stable disease, absence of recurrence, and lack of serious side effects. Etanercept appears to contribute to the control of inflammation and facilitate corticosteroid taper.
神经囊尾蚴病(NCC)的表现主要是由于宿主对驱虫药物损伤或自然退化的绦虫幼虫(囊肿)的炎症反应。在复杂疾病中,通常需要长时间大剂量使用皮质类固醇来控制这种炎症,这常常会导致严重的副作用。目前缺乏评估皮质类固醇替代药物的研究。在这里,我们描述了 16 例接受依那西普(ETN)治疗的神经囊尾蚴病患者的临床过程,ETN 是一种肿瘤坏死因子-α抑制剂,用于控制驱虫治疗引起的炎症。12 例脑外 NCC 患者接受 ETN 联合皮质类固醇(11/12,91.7%)和/或甲氨蝶呤(9/12,75.0%)治疗。脑外 NCC 亚组的中位年龄为 40 岁(范围 26-57 岁),66.7%为男性。他们接受 ETN 治疗的中位时间为 311 天(范围 31-461 天),然后中位随访时间为 3.4 年(范围 0.3-6.6 年)。在 9 例可评估的患者中,所有患者在开始使用 ETN 后临床均有改善,1 例短暂恶化。其余 3 例中,1 例失访,2 例患者病情改善但未完成规定疗程。另外 4 例复发性瘤周水肿(PE)患者接受 ETN 治疗,中位时间为 400.5 天(范围 366-854 天),ETN 治疗后中位随访时间为 1.7 年(范围 0.2-2.4 年)。所有 PE 患者均有改善,2 例成功减少了皮质类固醇的用量。ETN 治疗与临床改善、疾病稳定、无复发和无严重副作用有关。ETN 似乎有助于控制炎症并促进皮质类固醇的减量。