Department of Pathology and Microbiology, Aga Khan University, Karachi, Sindh, Pakistan.
PLoS One. 2013 Dec 4;8(12):e81363. doi: 10.1371/journal.pone.0081363. eCollection 2013.
Cytokine-mediated endothelial activation pathway is a known mechanism of pathogenesis employed by Plasmodium falciparum to induce severe disease symptoms in human host. Though considered benign, complicated cases of Plasmodium vivax are being reported worldwide and from Pakistan. It has been hypothesized that P.vivax utilizes similar mechanism of pathogenesis, as that of P.falciparum for manifestations of severe malaria. Therefore, the main objective of this study was to characterize the role of cytokines and endothelial activation markers in complicated Plasmodium vivax isolates from Pakistan.
A case control study using plasma samples from well-characterized groups suffering from P.vivax infection including uncomplicated cases (n=100), complicated cases (n=82) and healthy controls (n=100) were investigated. Base line levels of Tumor necrosis factor-α (TNF-α), Interleukin-6 (IL-6), Interleukin-10 (IL-10), Intercellular adhesion molecule-1 (ICAM-1), Vascular adhesion molecule-1(VCAM-1) and E-selectin were measured by ELISA. Correlation of cytokines and endothelial activation markers was done using Spearman's correlation analysis. Furthermore, significance of these biomarkers as indicators of disease severity was also analyzed. The results showed that TNF-α, IL-10, ICAM-1and VCAM-1 were 3-fold, 3.7 fold and 2 fold increased between uncomplicated and complicated cases. Comparison of healthy controls with uncomplicated cases showed no significant difference in TNF-α concentrations while IL-6, IL-10, ICAM-1, VCAM-1 and E-selectin were found to be elevated respectively. In addition, significant positive correlation was observed between TNF-α and IL-10/ ICAM-1, IL-6 and IL-10, ICAM-1 and VCAM-1.A Receiver operating curve (ROC) was generated which showed that TNF-α, IL-10, ICAM-1 and VCAM-1 were the best individual predictors of complicated P.vivax malaria.
The results suggest that though endothelial adhesion molecules are inducible by pro-inflammatory cytokine TNF-α, however, cytokine-mediated endothelial activation pathway is not clearly demonstrated as a mechanism of pathogenesis in complicated P.vivax malaria cases from Pakistan.
细胞因子介导的内皮激活途径是疟原虫引起人类宿主严重疾病症状的已知发病机制。虽然被认为是良性的,但世界各地和巴基斯坦都有报道称,复杂的间日疟病例。有人假设,间日疟原虫利用与恶性疟原虫类似的发病机制来表现出严重的疟疾。因此,本研究的主要目的是描述巴基斯坦复杂间日疟原虫分离株中细胞因子和内皮激活标志物的作用。
使用来自患有间日疟感染的特征明确的组的血浆样本进行病例对照研究,包括单纯病例(n=100)、复杂病例(n=82)和健康对照组(n=100)。通过 ELISA 测量肿瘤坏死因子-α(TNF-α)、白细胞介素-6(IL-6)、白细胞介素-10(IL-10)、细胞间黏附分子-1(ICAM-1)、血管细胞黏附分子-1(VCAM-1)和 E-选择素的基础水平。使用 Spearman 相关分析对细胞因子和内皮激活标志物进行相关性分析。此外,还分析了这些生物标志物作为疾病严重程度指标的意义。结果表明,TNF-α、IL-10、ICAM-1 和 VCAM-1 在单纯病例和复杂病例之间分别增加了 3 倍、3.7 倍和 2 倍。与单纯病例相比,健康对照组的 TNF-α浓度无显著差异,而 IL-6、IL-10、ICAM-1、VCAM-1 和 E-选择素均升高。此外,TNF-α与 IL-10/ICAM-1、IL-6 与 IL-10、ICAM-1 与 VCAM-1 之间存在显著正相关。生成了接收者操作曲线(ROC),显示 TNF-α、IL-10、ICAM-1 和 VCAM-1 是预测复杂间日疟的最佳个体标志物。
结果表明,尽管内皮黏附分子可被促炎细胞因子 TNF-α诱导,但细胞因子介导的内皮激活途径并不是巴基斯坦复杂间日疟病例发病机制的明确机制。