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对未接受机械通气的新型冠状病毒肺炎患者同情用药鲁索替尼:对炎症和通气的短期影响

Compassionate use of ruxolitinib in patients with SARS-Cov-2 infection not on mechanical ventilation: Short-term effects on inflammation and ventilation.

作者信息

Mortara Andrea, Mazzetti Simone, Margonato Davide, Delfino Pietro, Bersano Chiara, Catagnano Francesco, Lauriola Marinella, Grosso Paolo, Perseghin Gianluca, Ippoliti Giovanbattista

机构信息

Department of Clinical Cardiology, Policlinico di Monza, Monza, Italy.

Department of Cardiology, University of Pavia, Pavia, Italy.

出版信息

Clin Transl Sci. 2021 May;14(3):1062-1068. doi: 10.1111/cts.12971. Epub 2021 Jan 27.

DOI:10.1111/cts.12971
PMID:33403775
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8212747/
Abstract

Ruxolitinib is an anti-inflammatory drug that inhibits the Janus kinase-signal transducer (JAK-STAT) pathway on the surface of immune cells. The potential targeting of this pathway using JAK inhibitors is a promising approach in patients affected by coronavirus disease 2019 (COVID-19). Ruxolitinib was provided as a compassionate use in patients consecutively admitted to our institution for severe acute respiratory syndrome-coronavirus 2 (SARS-CoV-2) infection. Inclusion criteria were oxygen saturation less than or equal to 92%, signs of interstitial pneumonia, and no need of mechanical ventilation. Patients received 5 mg b.i.d. of ruxolitinib for 15 days, data were collected at baseline and on days 4, 7, and 15 during treatment. Two main targets were identified, C-reactive protein (CRP) and PaO /FiO ratio. In the 31 patients who received ruxolitinib, symptoms improved (dyspnea scale) on day 7 in 25 of 31 patients (80.6%); CRP decreased progressively from baseline (79.1 ± 73.4 mg/dl) to day 15 (18.6 ± 33.2, p = 0.022). In parallel with CRP, PO2/FiO ratio increased progressively during the 3 steps from 183 ± 95 to 361 ± 144 mmHg (p < 0.001). In those patients with a reduction of polymerase chain reaction less than or equal to 80%, delta increase of the PO2/FiO ratio was significantly more pronounced (129 ± 118 vs. 45 ± 35 mmHg, p = 0.02). No adverse side effects were recorded during treatment. In patients hospitalized for COVID-19, compassionate-use of ruxolitinib determined a significant reduction of biomarkers of inflammation, which was associated with a more effective ventilation and reduced need for oxygen support. Data on ruxolitinib reinforces the hypothesis that targeting the hyperinflammation state, may be of prognostic benefit in patients with SARS-CoV-2 infection. Study Highlights WHAT IS THE CURRENT KNOWLEDGE ON THE TOPIC? Some evidence suggest that patients affected by coronavirus disease 2019 (COVID-19) present an exuberant inflammatory response represented by a massive production of type I interferons and different pro-inflammatory cytokines. Nonetheless, as for the present, there are no proven therapeutic agents for COVID-19, in particular anti-inflammatory and antiviral, with a significant and reproducible positive clinical response. WHAT QUESTION DID THIS STUDY ADDRESS? Targeted therapeutic management of pro-inflammatory pathways appears to be a promising strategy against COVID-19, and ruxolitinib, due to its established broad and fast anti-inflammatory effect, appears to be a promising candidate worthy of focused investigations in this field. WHAT DOES THIS STUDY ADD TO OUR KNOWLEDGE? Ruxolitinib rapidly reduces the systemic inflammation, which accompanies the disease, thereby improving respiratory function and the need of oxygen support. This effect may contribute to avoid progression of the disease and the use of invasive ventilation. HOW MIGHT THIS CHANGE CLINICAL PHARMACOLOGY OR TRANSLATIONAL SCIENCE? Data on ruxolitinib contributes the reinforcement of the hypothesis that it is crucial to counteract the early hyperinflammation state, particularly of the lungs, induced by COVID-19 infection.

摘要

芦可替尼是一种抗炎药物,可抑制免疫细胞表面的Janus激酶-信号转导子(JAK-STAT)通路。使用JAK抑制剂靶向该通路对于2019冠状病毒病(COVID-19)患者来说是一种很有前景的方法。芦可替尼作为同情用药提供给因严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染而连续入住我们机构的患者。纳入标准为氧饱和度小于或等于92%、间质性肺炎体征且无需机械通气。患者接受每日两次、每次5mg的芦可替尼治疗,疗程为15天,在基线以及治疗期间的第4天、第7天和第15天收集数据。确定了两个主要指标,即C反应蛋白(CRP)和动脉血氧分压/吸入氧分数(PaO₂/FiO₂)比值。在31例接受芦可替尼治疗的患者中,31例患者中的25例(80.6%)在第7天症状改善(呼吸困难程度);CRP从基线(79.1±73.4mg/dl)逐渐下降至第15天(18.6±33.2,p = 0.022)。与CRP变化同步,PaO₂/FiO₂比值在三个阶段中逐渐升高,从183±95mmHg升至361±144mmHg(p < 0.001)。在那些聚合酶链反应降低小于或等于80%的患者中,PaO₂/FiO₂比值的增量显著更明显(129±118 vs. 45±35mmHg,p = 0.02)。治疗期间未记录到不良副作用。在因COVID-19住院的患者中,芦可替尼的同情用药显著降低了炎症生物标志物水平,这与更有效的通气和减少对氧支持的需求相关。关于芦可替尼的数据强化了这样一种假设,即靶向过度炎症状态可能对SARS-CoV-2感染患者具有预后益处。研究亮点 关于该主题目前的认知是什么?一些证据表明,2019冠状病毒病(COVID-19)患者表现出以大量产生I型干扰素和不同促炎细胞因子为特征的旺盛炎症反应。尽管如此,就目前而言,尚无经证实的对COVID-19有显著且可重复的积极临床反应的治疗药物,尤其是抗炎和抗病毒药物。 这项研究解决了什么问题?对促炎通路进行靶向治疗管理似乎是对抗COVID-19的一种有前景的策略,而芦可替尼因其已确立的广泛且快速的抗炎作用,似乎是该领域值得重点研究的一个有前景的候选药物。 这项研究为我们的知识增添了什么?芦可替尼能迅速减轻伴随该疾病的全身炎症,从而改善呼吸功能和对氧支持的需求。这种作用可能有助于避免疾病进展和使用有创通气。 这可能如何改变临床药理学或转化科学?关于芦可替尼的数据有助于强化这样一种假设,即对抗由COVID-19感染引起的早期过度炎症状态,尤其是肺部的过度炎症状态至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d44e/8212747/3131d81129af/CTS-14-1062-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d44e/8212747/40c1e85fd23c/CTS-14-1062-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d44e/8212747/3131d81129af/CTS-14-1062-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d44e/8212747/40c1e85fd23c/CTS-14-1062-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d44e/8212747/3131d81129af/CTS-14-1062-g002.jpg

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