Cavalier Etienne, Guiot Julien, Lechner Katharina, Dutsch Alexander, Eccleston Mark, Herzog Marielle, Bygott Thomas, Schomburg Adrian, Kelly Theresa, Holdenrieder Stefan
Clinical Chemistry Department, Centre Hospitalier Universitaire de Liege, Domaine Universitaire Du Sart-Tilman, Liège, Belgium.
Pneumology Department, Centre Hospitalier Universitaire de Liege, Domaine Universitaire Du Sart-Tilman, Liège, Belgium.
Front Mol Biosci. 2021 Mar 18;8:600881. doi: 10.3389/fmolb.2021.600881. eCollection 2021.
The severity of coronavirus disease 2019 (COVID-19) varies significantly with cases spanning from asymptomatic to lethal with a subset of individuals developing Severe Acute Respiratory Syndrome (SARS) and death from respiratory failure. To determine whether global nucleosome and citrullinated nucleosome levels were elevated in COVID-19 patients, we tested two independent cohorts of COVID-19 positive patients with quantitative nucleosome immunoassays and found that nucleosomes were highly elevated in plasma of COVID-19 patients with a severe course of the disease relative to healthy controls and that both histone 3.1 variant and citrullinated nucleosomes increase with disease severity. Elevated citrullination of circulating nucleosomes is indicative of neutrophil extracellular trap formation, neutrophil activation and NETosis in severely affected individuals. Importantly, using hospital setting (outpatient, inpatient or ICU) as a proxy for disease severity, nucleosome levels increased with disease severity and may serve as a guiding biomarker for treatment. Owing to the limited availability of mechanical ventilators and extracorporal membrane oxygenation (ECMO) equipment, there is an urgent need for effective tools to rapidly assess disease severity and guide treatment selection. Based on our studies of two independent cohorts of COVID-19 patients from Belgium and Germany, we suggest further investigation of circulating nucleosomes and citrullination as biomarkers for clinical triage, treatment allocation and clinical drug discovery.
2019冠状病毒病(COVID-19)的严重程度差异很大,病例范围从无症状到致命,部分患者会发展为严重急性呼吸综合征(SARS)并死于呼吸衰竭。为了确定COVID-19患者的全球核小体和瓜氨酸化核小体水平是否升高,我们使用定量核小体免疫测定法对两组独立的COVID-19阳性患者进行了检测,发现与健康对照相比,病情严重的COVID-19患者血浆中的核小体水平显著升高,并且组蛋白3.1变体和瓜氨酸化核小体均随疾病严重程度增加。循环核小体瓜氨酸化水平升高表明在受严重影响的个体中存在中性粒细胞胞外诱捕网形成、中性粒细胞活化和NETosis。重要的是,以医院环境(门诊、住院或重症监护病房)作为疾病严重程度的指标,核小体水平随疾病严重程度增加,可作为治疗的指导生物标志物。由于机械通气机和体外膜肺氧合(ECMO)设备的供应有限,迫切需要有效的工具来快速评估疾病严重程度并指导治疗选择。基于我们对来自比利时和德国的两组独立COVID-19患者队列的研究,我们建议进一步研究循环核小体和瓜氨酸化,将其作为临床分诊、治疗分配和临床药物发现的生物标志物。