Department of Viroscience, Erasmus University Medical Center, 3015 GD Rotterdam, The Netherlands.
Department for Clinical Microbiology, University Clinical Center of Republika Srpska, 78000 Banja Luka, Bosnia and Herzegovina.
Viruses. 2022 Jun 24;14(7):1377. doi: 10.3390/v14071377.
Puumala orthohantavirus (PUUV) is endemic in Europe and can cause hemorrhagic fever with renal syndrome (nephropathia epidemica). Disease features include fever, thrombocytopenia, and acute kidney injury (AKI). This retrospective cohort study of forty PUUV patients aims to characterize associations of serum immunological, hemostatic or kidney injury markers to disease severity. While interleukin-18 (IL-18) was significantly increased in severely thrombocytopenic patients (<100 × 109 platelets/L) compared to patients with higher platelet counts, RANTES was significantly decreased in these patients. These data suggest that patients with significant thrombocytopenia might have experienced pronounced Th1 immune responses. When kidney dysfunction was used as the primary disease outcome, recently identified AKI biomarkers (Cystatin C, insulin-like growth factor-binding protein 7, Nephrin, and trefoil factor 3) were significantly upregulated in patients with severe PUUV infection, defined as the estimated glomerular filtration rate (eGFR) below 30 m/min/1.73 m2. The increased expression of these markers specifically indicates pathology in glomeruli and proximal tubuli. Furthermore, E-selectin was significantly higher while interferon gamma-induced protein 10 (IP-10) was significantly lower in PUUV patients with more severe kidney dysfunction compared to patients with higher eGFR-values. Increased E-selectin illustrates the central role of endothelial cell activation, whereas decreased IP-10 could indicate a less important role of this cytokine in the pathogenesis of kidney dysfunction.
普马拉型正汉坦病毒(PUUV)在欧洲流行,可引起肾综合征出血热(流行性肾病)。疾病特征包括发热、血小板减少和急性肾损伤(AKI)。本研究对 40 例 PUUV 患者进行了回顾性队列研究,旨在探讨血清免疫、止血或肾损伤标志物与疾病严重程度的关系。与血小板计数较高的患者相比,严重血小板减少症(血小板计数<100×109/L)患者的白细胞介素-18(IL-18)显著升高,而 RANTES 在这些患者中显著降低。这些数据表明,血小板计数显著减少的患者可能经历了明显的 Th1 免疫反应。当肾功能障碍作为主要疾病结局时,最近确定的 AKI 生物标志物(胱抑素 C、胰岛素样生长因子结合蛋白 7、nephrin 和三叶因子 3)在严重 PUUV 感染患者中显著上调,严重 PUUV 感染定义为估计肾小球滤过率(eGFR)<30ml/min/1.73m2。这些标志物的表达增加表明肾小球和近端肾小管存在病理改变。此外,与 eGFR 值较高的患者相比,E-选择素在肾功能障碍较严重的 PUUV 患者中显著升高,而干扰素诱导蛋白 10(IP-10)显著降低。E-选择素的增加表明内皮细胞激活的核心作用,而 IP-10 的减少可能表明该细胞因子在肾功能障碍发病机制中的作用较小。