Weaver Lehn K, Behrens Edward M
Division of Pediatric Rheumatology, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
Curr Treatm Opt Rheumatol. 2017 Mar;3(1):33-48. doi: 10.1007/s40674-017-0059-x. Epub 2017 Feb 7.
Cytokine storm syndromes require rapid diagnosis and treatment to limit the morbidity and mortality caused by the hyperinflammatory state that characterizes these devastating conditions. Herein, we discuss the current knowledge that guides our therapeutic decision-making and personalization of treatment for patients with cytokine storm syndromes. Firstly, ICU-level supportive care is often required to stabilize patients with fulminant disease while additional diagnostic evaluations proceed to determine the underlying cause of cytokine storm. Pharmacologic interventions should be focused on removing the inciting trigger of inflammation and initiation of an individualized immunosuppressive regimen when immune activation is central to the underlying disease pathophysiology. Monitoring for a clinical response is required to ensure that changes in the therapeutic regimen can be made as clinically warranted. Escalation of immunosuppression may be required if patients respond poorly to the initial therapeutic interventions, while a slow wean of immunosuppression in patients who improve can limit medication-related toxicities. In certain scenarios, a decision must be made whether an individual patient requires hematopoietic cell transplantation to prevent recurrence of disease. Despite these interventions, significant morbidity and mortality remains for cytokine storm patients. Therefore, we use this review to propose a clinical schema to guide current and future attempts to design rational therapeutic interventions for patients suffering from these devastating conditions, which we believe speeds the diagnosis of disease, limits medication-related toxicities, and improves clinical outcomes by targeting the heterogeneous and dynamic mechanisms driving disease in each individual patient.
细胞因子风暴综合征需要迅速诊断和治疗,以限制由这些毁灭性疾病所特有的高炎症状态引起的发病率和死亡率。在此,我们讨论目前指导我们对细胞因子风暴综合征患者进行治疗决策和个性化治疗的知识。首先,对于暴发性疾病患者,往往需要重症监护病房(ICU)级别的支持性护理以使其病情稳定,同时进行进一步的诊断评估以确定细胞因子风暴的潜在病因。当免疫激活是潜在疾病病理生理学的核心时,药物干预应侧重于消除炎症的诱发因素,并启动个体化的免疫抑制方案。需要监测临床反应,以确保能够根据临床需要调整治疗方案。如果患者对初始治疗干预反应不佳,可能需要加强免疫抑制,而对于病情改善的患者,缓慢减少免疫抑制可限制药物相关毒性。在某些情况下,必须决定个别患者是否需要进行造血细胞移植以预防疾病复发。尽管采取了这些干预措施,细胞因子风暴患者的发病率和死亡率仍然很高。因此,我们利用本综述提出一种临床模式,以指导当前和未来为患有这些毁灭性疾病的患者设计合理治疗干预措施的尝试,我们认为这能够加快疾病诊断,限制药物相关毒性,并通过针对驱动每个患者疾病的异质性和动态机制来改善临床结果。