Andreas Angelopoulos, Ioannis Kouverianos, Dimitrios Daoussis
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引用次数: 0
摘要
导言嗜酸性粒细胞筋膜炎(EF)是一种罕见疾病,最初由舒尔曼(Shulman)于 1974 年提出,称为 "伴有嗜酸性粒细胞增多的弥漫性筋膜炎"。嗜酸性粒细胞性筋膜炎的症状包括外周嗜酸性粒细胞增多,伴有皮下筋膜和肌肉的对称性炎症,通常发生在上臂或大腿。目前还没有获得批准的标准治疗方法:考虑到嗜酸性粒细胞可能与 EF 的病因有关,我们在 Medline 上对 EF 的抗白细胞介素-5(IL-5)疗法进行了综述:结果:仅有一例 EF 患者成功接受了抗 IL-5 疗法--雷利珠单抗的治疗。该患者的EF对常用的免疫抑制疗法难治,但加入雷利珠单抗后,患者的症状得到缓解:讨论:EF 的确切病因尚不清楚,许多治疗方法已被证实。常用的免疫抑制剂,如皮质类固醇激素,并不总是有效,而且副作用很大。嗜酸性粒细胞似乎在该病的发病机制中起了一定作用;以 IL-5/IL-5 受体为靶点的抗嗜酸性粒细胞疗法可能是治疗该病的一种有吸引力的替代疗法。
Is there a Role for Anti-IL-5 Therapies in Eosinophilic Fasciitis?
Introduction: Eosinophilic Fasciitis (EF) is a rare disease, originally proposed as "diffuse fasciitis with eosinophilia" by Shulman in 1974. Symptoms of EF include peripheral eosinophilia accompanied by symmetrical inflammation of the subcutaneous fascia and muscle, usually locating in the upper arms or thighs. There is no approved standard of care treatment.
Methods: Taking into account that eosinophils may be pathogenetically involved in EF, we performed a review on Medline focusing on anti-Interleukin-5 (IL-5) therapies in EF.
Results: Only one case of a patient with EF has been reported who was successfully treated with reslizumab, an anti-IL-5 therapy. The patient had EF refractory to the commonly used immunosuppressive treatment but when reslizumab was added, the patient experienced remission of her symptoms.
Discussion: The exact aetiology of EF is still unclear, and many therapeutic approaches have been tested. Commonly used immunosuppressive agents, such as corticosteroids are not always effective and associate with significant side effects. Eosinophils seem to have a role in the pathogenesis of the disease; anti-eosinophilic therapies targeting IL-5/IL-5 Receptor could be an attractive alternative for the treatment of the disease.