Routsias John G, Marinou Dionysia, Mavrouli Maria, Tsakris Athanasios, Pitiriga Vassiliki C
Department of Microbiology, Medical School, National and Kapodistrian University of Athens, 11527 Athens, Greece.
Microorganisms. 2024 Aug 25;12(9):1762. doi: 10.3390/microorganisms12091762.
Vault particles are large cytoplasmic ribonucleoprotein particles that participate in inflammation. The aim of this study was to assess the diagnostic and prognostic value of major vault protein (MVP) in patients with inflammation, in order to determine whether MVP could be used as a biomarker for infection or inflammation. We also aimed to compare the diagnostic impact of MVP compared to other conventional measurements, such as CRP or white blood cell (WBC) counts.
CRP and MVP levels were measured in 111 sera samples from 85 patients with inflammation admitted to a tertiary-care hospital and 26 healthy individuals during an 18-month period (2019-2020), using nephelometry and a custom MVP sandwich ELISA assay, respectively. In addition, WBC counts were measured using a commercial assay.
MVP levels were found to be elevated in patients with inflammation compared to healthy individuals ( < 0.0001). Moreover, MVP levels were higher in patients with inflammation due to an infectious etiology compared to those with non-infectious etiology ( = 0.0006). MVP levels significantly decreased during the first four days of infection in response to antibiotic treatment, while CRP levels showed a less-sensitive decline. An ROC curve analysis demonstrated that MVP and CRP have similarly high diagnostic accuracy, with AUCs of 0.955 and 0.995, respectively, followed by WBCs with an AUC of 0.805.
The ROC curves demonstrated that MVP has the potential to serve as a diagnostic biomarker for inflammation and infection. Additionally, MVP levels may reflect the efficacy of antibiotic treatment.
穹窿体颗粒是参与炎症反应的大型细胞质核糖核蛋白颗粒。本研究旨在评估主要穹窿体蛋白(MVP)在炎症患者中的诊断和预后价值,以确定MVP是否可作为感染或炎症的生物标志物。我们还旨在比较MVP与其他传统检测指标(如C反应蛋白(CRP)或白细胞(WBC)计数)的诊断影响。
在18个月期间(2019 - 2020年),分别使用散射比浊法和定制的MVP夹心酶联免疫吸附测定法,对一家三级医院收治的85例炎症患者的111份血清样本以及26名健康个体的血清样本进行CRP和MVP水平检测。此外,使用商业检测方法测量WBC计数。
与健康个体相比,炎症患者的MVP水平升高(<0.0001)。此外,与非感染性病因引起的炎症患者相比,感染性病因引起的炎症患者的MVP水平更高(=0.0006)。在感染的前四天,MVP水平因抗生素治疗而显著下降,而CRP水平下降的敏感性较低。ROC曲线分析表明,MVP和CRP具有相似的高诊断准确性,AUC分别为0.955和0.995,其次是WBC,AUC为0.805。
ROC曲线表明MVP有潜力作为炎症和感染的诊断生物标志物。此外,MVP水平可能反映抗生素治疗的疗效。