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New biomarkers for stage determination in Trypanosoma brucei rhodesiense sleeping sickness patients

机译:用于布鲁氏锥虫罗非鱼昏睡病患者阶段测定的新生物标志物

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摘要

Accurate stage determination is crucial in the choice of treatment for patients suffering from sleeping sickness, also known as human African trypanosomiasis (HAT). Current staging methods, based on the counting of white blood cells (WBC) and the detection of parasites in the cerebrospinal fluid (CSF) have limited accuracy. We hypothesized that immune mediators reliable for staging T. b. gambiense HAT could also be used to stratify T. b. rhodesiense patients, the less common form of HAT.A population comprising 85 T. b. rhodesiense patients, 14 stage 1 (S1) and 71 stage 2 (S2) enrolled in Malawi and Uganda, was investigated. The CSF levels of IgM, MMP-9, CXCL13, CXCL10, ICAM-1, VCAM-1, neopterin and B2MG were measured and their staging performances evaluated using receiver operating characteristic (ROC) analyses.IgM, MMP-9 and CXCL13 were the most accurate markers for stage determination (partial AUC 88%, 86% and 85%, respectively). The combination in panels of three molecules comprising CXCL13-CXCL10-MMP-9 or CXCL13-CXCL10-IgM significantly increased their staging ability to partial AUC 94% (p value < 0.01).The present study highlighted new potential markers for stage determination of T. b. rhodesiense patients. Further investigations are needed to better evaluate these molecules, alone or in panels, as alternatives to WBC to make reliable choice of treatment.
机译:对于患有昏睡病(也称为人类非洲锥虫病(HAT))的患者,选择正确的治疗方法至关重要。基于白细胞计数(WBC)和脑脊液(CSF)中寄生虫检测的当前分期方法准确性有限。我们假设免疫介质可可靠地分期T。 gambiense HAT也可以用于对T进行分层。罗德岛病患者,是不常见的HAT.A人群,包括85T。调查了在马拉维和乌干达招募的14位1期(S1)和71位2期(S2)的罗得岛病患者。测量IgM,MMP-9,CXCL13,CXCL10,ICAM-1,VCAM-1,新蝶呤和B2MG的脑脊液水平,并使用接收器工作特征(ROC)分析评估其分期表现.IgM,MMP-9和CXCL13是最准确的阶段确定标记(部分AUC分别为88%,86%和85%)。包含CXCL13-CXCL10-MMP-9或CXCL13-CXCL10-IgM的三种分子的组合显着提高了其部分AUC的分期能力至94%(p值<0.01)。本研究强调了用于T分期确定的新潜在标志物b。罗得岛州患者。需要进一步研究以更好地评估这些分子(单独或以小组形式),作为WBC的替代品以做出可靠的治疗选择。

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