Hufnagel Katrin, Fathi Anahita, Stroh Nadine, Klein Marco, Skwirblies Florian, Girgis Ramy, Dahlke Christine, Hoheisel Jörg D, Lowy Camille, Schmidt Ronny, Griesbeck Anne, Merle Uta, Addo Marylyn M, Schröder Christoph
Sciomics GmbH, Neckargemünd, Baden-Württemberg, Germany.
University Medical Center Hamburg-Eppendorf, Institute for Infection Research and Vaccine Development (IIRVD), Hamburg, Germany.
Commun Med (Lond). 2023 Apr 12;3(1):51. doi: 10.1038/s43856-023-00283-z.
The clinical course of COVID-19 patients ranges from asymptomatic infection, via mild and moderate illness, to severe disease and even fatal outcome. Biomarkers which enable an early prediction of the severity of COVID-19 progression, would be enormously beneficial to guide patient care and early intervention prior to hospitalization.
Here we describe the identification of plasma protein biomarkers using an antibody microarray-based approach in order to predict a severe cause of a COVID-19 disease already in an early phase of SARS-CoV-2 infection. To this end, plasma samples from two independent cohorts were analyzed by antibody microarrays targeting up to 998 different proteins.
In total, we identified 11 promising protein biomarker candidates to predict disease severity during an early phase of COVID-19 infection coherently in both analyzed cohorts. A set of four (S100A8/A9, TSP1, FINC, IFNL1), and two sets of three proteins (S100A8/A9, TSP1, ERBB2 and S100A8/A9, TSP1, IFNL1) were selected using machine learning as multimarker panels with sufficient accuracy for the implementation in a prognostic test.
Using these biomarkers, patients at high risk of developing a severe or critical disease may be selected for treatment with specialized therapeutic options such as neutralizing antibodies or antivirals. Early therapy through early stratification may not only have a positive impact on the outcome of individual COVID-19 patients but could additionally prevent hospitals from being overwhelmed in potential future pandemic situations.
新型冠状病毒肺炎(COVID-19)患者的临床病程范围从无症状感染,到轻症和中症,再到重症甚至死亡。能够早期预测COVID-19病情严重程度的生物标志物,对于指导患者护理以及在住院前进行早期干预将极为有益。
在此,我们描述了使用基于抗体微阵列的方法来鉴定血浆蛋白生物标志物,以便在严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染的早期阶段预测COVID-19疾病的严重病因。为此,通过针对多达998种不同蛋白质的抗体微阵列分析了来自两个独立队列的血浆样本。
总体而言,我们在两个分析队列中一致鉴定出11种有前景的蛋白质生物标志物候选物,以预测COVID-19感染早期阶段的疾病严重程度。使用机器学习选择了一组四种蛋白质(S100A8/A9、血小板反应蛋白1、纤维连接蛋白C、干扰素λ1)以及两组三种蛋白质(S100A8/A9、血小板反应蛋白1、表皮生长因子受体2和S100A8/A9、血小板反应蛋白1、干扰素λ1)作为多标志物组合,其准确性足以用于预后测试。
利用这些生物标志物,可以选择有发展为重症或危重症疾病高风险的患者,采用诸如中和抗体或抗病毒药物等专门的治疗方案进行治疗。通过早期分层进行早期治疗不仅可能对个体COVID-19患者的预后产生积极影响,还可以防止医院在未来可能出现的大流行情况下不堪重负。