Jeewandara Chandima, Gomes Laksiri, Wickramasinghe N, Gutowska-Owsiak Danuta, Waithe Dominic, Paranavitane S A, Shyamali N L A, Ogg Graham S, Malavige Gathsaurie Neelika
Centre for Dengue Research, University of Sri Jayawardanapura, Nugegoda, Sri Lanka; MRC Human Immunology Unit, NIHR Biomedical Research Centre, Weatherall Institute of Molecular Medicine, Oxford, United Kingdom.
Centre for Dengue Research, University of Sri Jayawardanapura, Nugegoda, Sri Lanka.
PLoS Negl Trop Dis. 2015 Feb 3;9(2):e0003459. doi: 10.1371/journal.pntd.0003459. eCollection 2015 Feb.
Although plasma leakage is the hallmark of severe dengue infections, the factors that cause increased vascular permeability have not been identified. As platelet activating factor (PAF) is associated with an increase in vascular permeability in other diseases, we set out to investigate its role in acute dengue infection.
PAF levels were initially assessed in 25 patients with acute dengue infection to determine if they were increased in acute dengue. For investigation of the kinetics of PAF, serial PAF values were assessed in 36 patients. The effect of dengue serum on tight junction protein ZO-1 was determined by using human endothelial cell lines (HUVECs). The effect of dengue serum on and trans-endothelial resistance (TEER) was also measured on HUVECs.
PAF levels were significantly higher in patients with acute dengue (n = 25; p = 0.001) when compared to healthy individuals (n = 12). In further investigation of the kinetics of PAF in serial blood samples of patients (n = 36), PAF levels rose just before the onset of the critical phase. PAF levels were significantly higher in patients with evidence of vascular leak throughout the course of the illness when compared to those with milder disease. Serum from patients with dengue significantly down-regulated expression of tight junction protein, ZO-1 (p = 0.004), HUVECs. This was significantly inhibited (p = 0.004) by use of a PAF receptor (PAFR) blocker. Serum from dengue patients also significantly reduced TEER and this reduction was also significantly (p = 0.02) inhibited by prior incubation with the PAFR blocker.
Our results suggest the PAF is likely to be playing a significant role in inducing vascular leak in acute dengue infection which offers a potential target for therapeutic intervention.
尽管血浆渗漏是严重登革热感染的标志,但导致血管通透性增加的因素尚未明确。由于血小板活化因子(PAF)在其他疾病中与血管通透性增加有关,我们着手研究其在急性登革热感染中的作用。
最初对25例急性登革热感染患者的PAF水平进行评估,以确定其在急性登革热中是否升高。为研究PAF的动力学,对36例患者的PAF值进行连续评估。使用人内皮细胞系(HUVECs)确定登革热血清对紧密连接蛋白ZO-1的影响。还在HUVECs上测量登革热血清对跨内皮电阻(TEER)的影响。
与健康个体(n = 12)相比,急性登革热患者(n = 25)的PAF水平显著更高(p = 0.001)。在对患者连续血样(n = 36)中PAF动力学的进一步研究中,PAF水平在关键期开始前升高。与病情较轻的患者相比,在疾病全过程中有血管渗漏证据的患者PAF水平显著更高。登革热患者的血清显著下调紧密连接蛋白ZO-1在HUVECs中的表达(p = 0.004)。使用PAF受体(PAFR)阻滞剂可显著抑制这一现象(p = 0.004)。登革热患者的血清也显著降低TEER,且预先用PAFR阻滞剂孵育可显著抑制这种降低(p = 0.02)。
我们的结果表明,PAF可能在急性登革热感染中诱导血管渗漏方面发挥重要作用,这为治疗干预提供了一个潜在靶点。