结核病诊断和预后的潜在免疫生物标志物

Yassameen A. Hussain, K. Mohammed, N. Ali
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引用次数: 0

摘要

结核病(TB)是世界上最常见的传染病之一,已导致许多人死亡。因此,开发一种有效的诊断方法对于监测和控制这些致命的传染病至关重要。本研究分别采用ELISA和qPCR技术,评价血清4种炎症标志物(CXCL10、CXCL9、suPAR和MMP9)水平和NF-κB基因表达作为结核病诊断和预后的潜在免疫学标志物。本研究招募了30名新发结核病患者以及同等数量的正在接受治疗的结核病患者和对照组(健康人群)。结果显示,三组患者血清CXCL10水平差异有统计学意义(p值0.003),新患者与治疗中的患者血清CXCL10水平差异有统计学意义(p值0.004)。新发结核患者血清CXCL9水平与健康组差异有统计学意义(p值为0.028),而新发结核患者与正在治疗的结核患者血清CXCL9水平未达到统计学意义(p值为0.028)。新发患者血清suPAR水平最高(106.59pg/ml),治疗组次之(89.66pg/ml),健康组最低(80.71pg/ml),但未达到显著水平。此外,血清MMP-9水平在实验组之间没有显着差异,但新患者的血清MMP-9水平(21.45ng/ml)略高于健康组(20.70ng/ml)。与健康人群相比,新发患者NF-κB基因表达量(变化8.21倍)明显高于治疗前患者(变化2.95倍)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Potential Immunological Biomarker for Diagnosis and Prognosis of Tuberculosis
Tuberculosis (TB) is one of the most common infectious diseases in the world, which has led to numerous deaths. Hence, developing an efficient diagnostic method is essential to monitor and control such deadly infectious diseases. In the current study, the serum levels of four inflammatory markers (CXCL10, CXCL9, suPAR, and MMP9) and the expression NF-κB gene were evaluated as potential immunological markers for diagnosis and prognosis of tuberculosis, using ELISA and qPCR technique respectively. Thirty new TB patients and equal numbers of under treatment TB patients and control (healthy people) were conscripted in this study. The results showed significant differences in the serum level of CXCL10 among the three groups (p value 0.003) and between new and under treatment patients (P value 0.004). A significant difference in the CXCL9 level in the serum was observed between the new TB patients and the healthy group with p value 0.028 but didn’t reach the significant level between the new and under treatment patients.  The serum level of suPAR was higher in new patients (106.59pg/ml) followed by treated patients (89.66pg/ml) and lowest in healthy group (80.71pg/ml) but didn’t reach the significant level. Also, the serum level of MMP-9 did not show a significant difference between the tested groups, but it was slightly higher in new patients (21.45ng/ml) compared to the healthy group (20.70ng/ml). The amount of NF-κB gene expression was significantly higher in new patients (8.21-fold change) than in under treatment patients (2.95-fold change) in comparing with healthy people.
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