Ali Zain, Waseem Shahid, Anis Riffat Aysha, Anees Mariam
Zain Ali, MPhil. Department of Biochemistry, Quaid-i-Azam University, Islamabad, Pakistan.
Shahid Waseem, Ph.D. Alpha Genomics Private Limited, Islamabad, Pakistan.
Pak J Med Sci. 2020 Jul-Aug;36(5):860-866. doi: 10.12669/pjms.36.5.2476.
Cell Free mitochondrial DNA (CF mt-DNA) has emerged as a novel biomarker to investigate disease pathophysiology of different infections. The present study was designed to elucidate the association between CF mt-DNA, IL-6 and viral load in HIV, HBV and HCV infections and predict its role as a potential biomarker to assess the disease severity in viral infections.
Total 120 blood samples were collected from January 2018 to December 2018 of HIV, HBV and HCV patients and healthy controls (30 samples in each group). DNA and RNA were extracted from the serum to determine the levels of CF mt-DNA and viral load, respectively. IL-6 from the serum of infected individuals was quantified with ELISA.
HCV patients showed the highest levels of CF mt-DNA, IL-6 and viral load, followed by HBV and HIV. Significant correlation was found between CF mt-DNA and IL-6 among the HBV patients (p=0.017). However, no significant correlation of CF mt-DNA was observed with IL-6 in HIV and HCV or with the viral load in any of the three infections.
Elevated CF mt-DNA indicates its role in severity of viral infections. Independence of CF mt-DNA expression from viral load and IL-6 in case of HIV and HCV suggests involvement of other inflammatory pathways regulating CF mt-DNA elevation.
游离线粒体DNA(CF mt-DNA)已成为一种用于研究不同感染疾病病理生理学的新型生物标志物。本研究旨在阐明CF mt-DNA、白细胞介素-6(IL-6)与HIV、HBV和HCV感染中病毒载量之间的关联,并预测其作为评估病毒感染疾病严重程度的潜在生物标志物的作用。
于2018年1月至2018年12月收集了120份血液样本,包括HIV、HBV和HCV患者以及健康对照者(每组30份样本)。分别从血清中提取DNA和RNA,以测定CF mt-DNA水平和病毒载量。采用酶联免疫吸附测定法(ELISA)对感染个体血清中的IL-6进行定量分析。
HCV患者的CF mt-DNA、IL-6和病毒载量水平最高,其次是HBV和HIV患者。在HBV患者中,CF mt-DNA与IL-6之间存在显著相关性(p = 0.017)。然而,在HIV和HCV患者中,未观察到CF mt-DNA与IL-6之间存在显著相关性,且在这三种感染中的任何一种中,CF mt-DNA与病毒载量之间也无显著相关性。
CF mt-DNA升高表明其在病毒感染严重程度中发挥作用。在HIV和HCV感染中,CF mt-DNA表达独立于病毒载量和IL-6,这表明其他炎症途径参与调节CF mt-DNA升高。