Laboratory of Molecular Virology and Oncology, Department of Bioengineering and Technology, Gauhati University Institute of Science and Technology, Gauhati University, Guwahati, India.
Department of Gastroenterology, Gauhati Medical College and Hospital, Guwahati, India.
Viral Immunol. 2020 Jul/Aug;33(6):457-467. doi: 10.1089/vim.2019.0170. Epub 2020 Apr 29.
Chronic hepatitis C virus (HCV) infection leads to variable outcomes, ranging from prolonged slow hepatic damage leading to cirrhosis, and hepatocellular carcinoma (HCC). Polymorphism in cytokines IL-10 and IL-12 that impact the immune response to HCV infection may play a role in determining this outcome. This study was aimed to determine if polymorphisms in and contribute to HCV susceptibility and the risk of developing HCC in patients from Northeast India. - 1082, -819, -592 polymorphisms and -1188 polymorphisms were genotyped by polymerase chain reaction-restriction fragment length polymorphism in a total of 266 HCV-infected patients and 100 age- and sex-matched controls. In the HCV-infected subjects, 110 patients had chronic hepatitis C (CHC), 96 with liver cirrhosis, and 60 with HCC. Serum levels of were also measured and correlated with disease severity. Haplotype analysis for polymorphisms was carried out. Statistical data were analyzed using SPSS ver. 22.0. The frequency of - 592 AA genotype/A allele was significantly higher in HCC patients than in CHC patients. The intermediate IL-10-producing ACC haplotype was significantly more frequent in HCC and cirrhotic patients than in CHC patients. No significant association was found for - 819, -592 and -1188 polymorphisms with the susceptibility to HCV infection or occurrence of HCC in HCV-infected patients. - 592 CA polymorphism and ACC haplotype are significant biomarkers of HCC in HCV-infected patients from Northeast India. Higher serum levels of IL-10 were also linked to higher disease severity.
慢性丙型肝炎病毒(HCV)感染导致的结局各不相同,从导致肝硬化和肝细胞癌(HCC)的长期缓慢肝损伤到 HCC。细胞因子 IL-10 和 IL-12 的多态性影响对 HCV 感染的免疫反应,可能在决定这一结果方面发挥作用。本研究旨在确定 和 中的多态性是否导致印度东北部 HCV 感染者易感性增加,并增加其发生 HCC 的风险。通过聚合酶链反应-限制性片段长度多态性,对 266 例 HCV 感染患者和 100 名年龄和性别匹配的对照者进行了 -1082、-819、-592 多态性和 -1188 多态性的基因分型。在 HCV 感染患者中,110 例为慢性丙型肝炎(CHC),96 例为肝硬化,60 例为 HCC。还测量了 HCV 感染患者的血清 水平,并将其与疾病严重程度相关联。对 多态性进行了单体型分析。使用 SPSS ver. 22.0 分析统计数据。与 CHC 患者相比,HCC 患者的 -592 AA 基因型/等位基因频率显著升高。中间 IL-10 产生的 ACC 单体型在 HCC 和肝硬化患者中比在 CHC 患者中更为常见。未发现 -819、-592 和 -1188 多态性与 HCV 感染易感性或 HCV 感染患者 HCC 的发生有显著关联。-592 CA 多态性和 ACC 单体型是印度东北部 HCV 感染患者 HCC 的重要生物标志物。较高的血清 IL-10 水平也与较高的疾病严重程度有关。