Department of Laboratory Medicine and Pathobiology, University of Toronto, Toronto, ON, Canada.
Sandra A. Rotman (SAR) Laboratories, Sandra Rotman Centre for Global Health, University Health Network-Toronto General Hospital, Toronto, ON, Canada.
Front Immunol. 2022 Jun 10;13:931321. doi: 10.3389/fimmu.2022.931321. eCollection 2022.
Severe malaria (SM) is a leading cause of global morbidity and mortality, particularly in children in sub-Saharan Africa. However, existing malaria diagnostic tests do not reliably identify children at risk of severe and fatal outcomes. Dysregulated host immune and endothelial activation contributes to the pathogenesis of SM. Current research suggests that measuring markers of these pathways at presentation may have clinical utility as prognostic indicators of disease progression and risk of death. In this review, we focus on the available evidence implicating soluble urokinase-type plasminogen activator receptor (suPAR) as a novel and early predictor of severe and fatal malaria and discuss its potential utility for malaria triage and management.
严重疟疾(SM)是全球发病率和死亡率的主要原因,特别是在撒哈拉以南非洲的儿童中。然而,现有的疟疾诊断检测方法并不能可靠地识别出有发生严重和致命后果风险的儿童。宿主免疫和内皮细胞激活失调是 SM 发病机制的一部分。目前的研究表明,在出现时测量这些途径的标志物可能具有临床效用,可以作为疾病进展和死亡风险的预后指标。在这篇综述中,我们重点关注了可溶性尿激酶型纤溶酶原激活物受体(suPAR)作为严重和致命疟疾的新型早期预测因子的现有证据,并讨论了其在疟疾分诊和管理方面的潜在应用。