在成人斯蒂尔病中抑制炎性细胞因子。当前趋势和新的治疗前景

Pub Date : 2019-12-02 DOI:10.1080/21678707.2019.1701431
P. Ruscitti, A. Conforti, V. Pavlych, R. Giacomelli
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引用次数: 0

摘要

摘要:多项证据表明,抑制炎症细胞因子在成人发病斯蒂尔病(AOSD)患者中的临床应用价值。斯蒂尔病是一种罕见的炎症性疾病。对糖皮质激素和合成疾病缓解抗风湿药物(DMARDs)的第一种治疗策略缺乏反应确定了“难治性患者”,随后用生物DMARDs治疗。涉及领域:本文回顾了针对炎症细胞因子的生物DMARDs在AOSD中的临床应用,分析了目前的趋势,并提出了未来的治疗前景。专家意见:AOSD的治疗管理是针对炎症体征和症状,预防危及生命的并发症,并尽量减少免疫抑制治疗的不良反应。在此背景下,在过去的十年中,抑制炎症细胞因子的临床用途已经在AOSD中显示出多种益处,因为很大比例的患者获得了临床反应。抑制炎症细胞因子也可能有助于控制危及生命的AOSD并发症。展望未来,这一领域的研究正在迅速发展,在未来,正在进行的随机对照试验的结果和临床工具的开发很容易在临床实践中转移,将改善AOSD的管理,提供更有针对性的治疗,改善这些患者的预后。
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Inhibiting inflammatory cytokines in adult onset Still’s disease. Current trends and new therapeutic perspectives
ABSTRACT Introduction: Multiple lines of evidence suggest the clinical usefulness of inhibiting inflammatory cytokines in patients affected by adult onset Still’s disease (AOSD), a rare inflammatory disease. The lack of response to the first therapeutic strategy with glucocorticoids and synthetic disease-modifying anti-rheumatic drugs (DMARDs) identifies ‘refractory patients’, to be subsequently treated with biologic DMARDs. Areas covered: In this article, evidence has been reviewed about the clinical usefulness of biologic DMARDs, targeting inflammatory cytokines, in AOSD, analyzing current trends and suggesting future therapeutic perspectives. Expert opinion: Therapeutic management of AOSD is directed at targeting inflammatory signs and symptoms, preventing life-threating complications, and minimizing the adverse effects of immunosuppressive therapies. In this context, over the last decade, the clinical usefulness of inhibiting inflammatory cytokines has shown in AOSD with multiple benefits, since a large percentage of patients attain a clinical response. The inhibition of inflammatory cytokines could also be helpful in managing life-threating complications of AOSD. Going forward, this field of research is rapidly growing, and in the next future, the results about ongoing randomized controlled trials and the development of clinical tools readily transferable in clinical practice, would improve the management of AOSD providing more targeted treatment and improving the outcomes of these patients.
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