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白细胞介素-1 受体拮抗剂(阿那白滞素)成功治疗血管滤泡性淋巴结增生症。

Successful treatment of Castleman's disease with interleukin-1 receptor antagonist (Anakinra).

机构信息

Department of Investigational Cancer Therapeutics, (Phase I Clinical Trials Program), The University of Texas, M.D. Anderson Cancer Center, Houston, Texas 77030, USA.

出版信息

Mol Cancer Ther. 2010 Jun;9(6):1485-8. doi: 10.1158/1535-7163.MCT-10-0156. Epub 2010 May 25.

Abstract

Castleman's disease (CD) is a very rare lymphoproliferative disorder whose underlying pathophysiology is not fully understood and for which no standard treatment exists. Because interleukin-1 (IL-1) might promote the production of interleukin-6 (IL-6), a key pathogenic factor for the disease, we hypothesized that blocking the interleukin-1 receptor would be a useful therapy for CD. We report the case of a 61-year-old woman with CD who had undergone multiple treatments, including cladribine, rituximab, steroids, etanercept, and anti-IL-6 monoclonal antibody, and whose disease was refractory to all of these treatments. She was started on the recombinant IL-1 receptor antagonist, Anakinra, at a subcutaneous dose of 100 mg daily. Within one week, her fatigue and anorexia markedly improved, and her laboratory abnormalities, including anemia, thrombocytosis, leukocytosis, and elevated markers of inflammation, all resolved. Our observation suggests that Anakinra may be an attractive therapeutic approach for refractory multicentric CD.

摘要

卡斯尔曼病 (CD) 是一种非常罕见的淋巴组织增生性疾病,其潜在的病理生理学尚未完全阐明,也没有标准的治疗方法。由于白细胞介素-1 (IL-1) 可能促进疾病关键致病因子白细胞介素-6 (IL-6) 的产生,我们假设阻断白细胞介素-1 受体将是治疗 CD 的一种有效方法。我们报告了一例 61 岁女性 CD 患者,她曾接受多种治疗,包括克拉屈滨、利妥昔单抗、类固醇、依那西普和抗 IL-6 单克隆抗体,但这些治疗对她的疾病均无效。她开始每天皮下注射 100mg 的重组白细胞介素-1 受体拮抗剂阿那白滞素。一周内,她的疲劳和食欲不振明显改善,她的实验室异常,包括贫血、血小板增多、白细胞增多和炎症标志物升高,都得到了缓解。我们的观察结果表明,阿那白滞素可能是治疗难治性多中心 CD 的一种有吸引力的治疗方法。

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