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白细胞介素-6阻断与JAK-STAT抑制在预防COVID-19患者肺损伤中的比较

Interleukin-6 Blocking vs. JAK-STAT Inhibition for Prevention of Lung Injury in Patients with COVID-19.

作者信息

Meletiadis Joseph, Tsiodras Sotirios, Tsirigotis Panagiotis

机构信息

Clinical Microbiology Laboratory, Attikon University Hospital, Medical School, National and Kapodistrian University of Athens, Athens, Greece.

Forth Department of Internal Medicine, Attikon University Hospital, Medical School, National and Kapodistrian University of Athens, Athens, Greece.

出版信息

Infect Dis Ther. 2020 Dec;9(4):707-713. doi: 10.1007/s40121-020-00326-1. Epub 2020 Aug 12.

Abstract

The severe respiratory insufficiency observed during COVID-19 infection may not be directly related to a cytopathogenic effect induced by the virus itself, but to an exaggerated and inappropriate immune response. In an effort to reduce the severity of organ dysfunction, including respiratory insufficiency, monoclonal antibodies (Mabs) that block the interleukin-6 receptor, such as tocilizumab, sarilumab, and siltuximab, are under investigation for the treatment of COVID-19. However, blocking of just one of the many cytokines involved in the inflammatory reaction may not slow down the magnitude of the process. Since timing is important, the immune deficiency induced by IL6 blockade at the late immunodeficiency phase of sepsis that follows the initial inflammatory response may be detrimental. Finally, monitoring the degree and duration of IL6 blockade may be challenging because of the long half-life of Mabs (2-3 weeks). Pro- and anti-inflammatory cytokines act through a common JAK-STAT signaling pathway, which can be inhibited by JAK-STAT inhibitors. Ruxolitinib, a tyrosine kinase inhibitor selective for JAK1, 2, blocks many pro- and anti-inflammatory cytokines including IL6. Ruxolitinib has favorable pharmacodynamics and an acceptable safety profile. The short half-life (4-6 h) of the drug offers the opportunity for ideal monitoring of the degree and duration of cytokine blocking, simply by the adjusting dose and duration of therapy. From a theoretical point of view, the balanced control of cytokine blockade throughout the course of the septic process should be the cornerstone of modern management. According to this hypothesis, maximization of blocking should be attempted at the phase of hyper-inflammation for preventing severe organ damage, while pro-inflammatory blockade should be minimized at the late phase of immunoparalysis for prevention of secondary infections. Based on the above considerations, we consider that the efficacy and safety of this drug deserves testing in the context of a controlled randomized trial.

摘要

新型冠状病毒肺炎(COVID-19)感染期间观察到的严重呼吸功能不全可能并非直接与病毒本身诱导的细胞病变效应相关,而是与过度且不适当的免疫反应有关。为了降低包括呼吸功能不全在内的器官功能障碍的严重程度,正在研究使用阻断白细胞介素-6受体的单克隆抗体(Mab),如托珠单抗、萨瑞鲁单抗和西妥昔单抗,用于治疗COVID-19。然而,阻断炎症反应中众多细胞因子中的一种可能无法减缓该过程的程度。由于时机很重要,在脓毒症初始炎症反应后的免疫缺陷后期阶段,IL6阻断诱导的免疫缺陷可能是有害的。最后,由于Mab的半衰期较长(2 - 3周),监测IL6阻断的程度和持续时间可能具有挑战性。促炎和抗炎细胞因子通过共同的JAK - STAT信号通路发挥作用,该通路可被JAK - STAT抑制剂抑制。芦可替尼是一种对JAK1、2具有选择性的酪氨酸激酶抑制剂,可阻断包括IL6在内的许多促炎和抗炎细胞因子。芦可替尼具有良好的药效学和可接受的安全性。该药物较短的半衰期(4 - 6小时)提供了通过调整治疗剂量和持续时间来理想监测细胞因子阻断程度和持续时间的机会。从理论角度来看,在整个脓毒症过程中对细胞因子阻断进行平衡控制应是现代治疗的基石。根据这一假设,应在炎症过度阶段尝试最大程度地阻断,以预防严重器官损伤,而在免疫麻痹后期应尽量减少促炎阻断,以预防继发感染。基于上述考虑,我们认为该药物的疗效和安全性值得在对照随机试验的背景下进行测试。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2270/7680461/d25dd76f3cd0/40121_2020_326_Fig1_HTML.jpg

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