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一种针对成年斯蒂尔病并发症肺动脉高压的新型治疗方法:靶向白细胞介素-6。

A novel therapeutic approach in pulmonary arterial hypertension as a complication of adult-onset Still's disease: targeting IL-6.

作者信息

Kadavath Sabeeda, Zapantis Ekaterini, Zolty Ronald, Efthimiou Petros

机构信息

Rheumatology Division, Lincoln Medical and Mental Health Center, New York, New York, USA.

出版信息

Int J Rheum Dis. 2014 Mar;17(3):336-40. doi: 10.1111/1756-185X.12324. Epub 2014 Feb 28.

Abstract

Adult-onset Still's Disease (AOSD), often though as the adult variant of systemic juvenile idiopathic arthritis (JIA), has an incidence of 1-3 cases per 1 million. Cardinal manifestations include fever, arthritis, skin rash, sore throat, hepatosplenomegaly and lymphadenopathy. Prolongation in diagnosing this disease results from its similarity to infectious, malignant and rheumatic diseases and lack of biomarkers. Pulmonary arterial hypertension (PAH) is a rare pulmonary complication of AOSD, and we are aware of only six cases reported in literature to date. Here we present a patient with AOSD who has developed pulmonary hypertension as a complication. We report a case of AOSD complicated by PAH treated successfully with tocilizumab, a humanized monoclonal antibody to human interleukin (IL)-6 receptor. A Pubmed and Medline search for evidence of pulmonary hypertension in AOSD and use of IL-6 inhibition in management was performed. Data for this study was collected from the patient's chart records. No infectious or neoplastic cause of her disease was identified and after extensive diagnostic workup, the patient was diagnosed with AOSD fulfilling Yamaguchi criteria. After initiation of IL-6 therapy the patient was followed over time to monitor the hemodynamic changes in pulmonary vasculature. Following treatment with Tocilizumab, the patient showed dramatic improvement in her clinical symptoms and remains in remission, through combination of tocilizumab (8 mg/kg), methotrexate and prednisone. Improvement of systemic symptoms, right heart catheterization (RHC) findings and the VECTRA-DA score served as a measure of treatment response. Tocilizumab has been effective in demonstrating marked improvement in both the clinical and laboratory parameters. Tocilizumab is an effective novel treatment for AOSD with PAH. This is the first documented report of successful use of tocilizumab in AOSD patients presenting with PAH. Prospective comparative studies could help validate its efficacy and safety.

摘要

成人斯蒂尔病(AOSD)通常被认为是系统性幼年特发性关节炎(JIA)的成人变异型,发病率为每100万人中有1 - 3例。主要表现包括发热、关节炎、皮疹、咽痛、肝脾肿大和淋巴结病。由于该病与感染性、恶性和风湿性疾病相似且缺乏生物标志物,导致诊断延迟。肺动脉高压(PAH)是AOSD罕见的肺部并发症,迄今为止我们仅知晓文献报道的6例。在此,我们报告1例并发肺动脉高压的AOSD患者。我们报告1例AOSD并发PAH的病例,该患者接受抗人白细胞介素(IL)-6受体的人源化单克隆抗体托珠单抗成功治疗。我们在PubMed和Medline上检索了AOSD中肺动脉高压的证据以及IL - 6抑制在治疗中的应用。本研究的数据收集自患者的病历记录。未发现其疾病的感染性或肿瘤性病因,经过广泛的诊断检查,该患者被诊断为符合山口标准的AOSD。在开始IL - 6治疗后,对患者进行长期随访以监测肺血管系统的血流动力学变化。使用托珠单抗治疗后,通过联合使用托珠单抗(8 mg/kg)、甲氨蝶呤和泼尼松,患者的临床症状显著改善并持续缓解。全身症状的改善、右心导管检查(RHC)结果和VECTRA - DA评分作为治疗反应的衡量指标。托珠单抗已有效证明在临床和实验室参数方面均有显著改善。托珠单抗是治疗AOSD并发PAH的一种有效的新型疗法。这是首次记录成功使用托珠单抗治疗并发PAH的AOSD患者的报告。前瞻性比较研究有助于验证其疗效和安全性。

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