Nabeel Mohamed M, Darwish Rania K, Alakel Wafaa, Maher Rabab, Mostafa Hossam, Hashem Ahmed, Elbeshlawy Mohamed, Abul-Fotouh Amr, Shousha Hend I, Saeed Marie Mohamad
Endemic Medicine and Hepatogastroenterology Department, Faculty of Medicine, Cairo University, Cairo, Egypt.
Clinical and Chemical Pathology Department, Faculty of Medicine, Cairo University, Cairo, Egypt.
J Clin Exp Hepatol. 2022 Mar-Apr;12(2):428-434. doi: 10.1016/j.jceh.2021.06.018. Epub 2021 Jun 25.
This study analyzes the changing levels of circulating inflammatory cytokines Interferon gamma (IFN-γ) and interleukin (IL)-10 (as the main cytokines of T-helper-1 and T-helper-2 immune responses) in patients with chronic hepatitis C virus (HCV) infection undergoing therapy with direct-acting antivirals (DAAs) and to correlate them with laboratory markers.
This Pilot study included 50 HCV monoinfected patients who received DAAs for 12 or 24 weeks. They were followed up monthly during therapy and 3 months after the end of the treatment. Liver disease was determined by transient elastography, in addition to FIB-4 indices. Analysis of IFN-gamma and IL-10 was carried out using an enzyme-linked immunosorbent assay.
All patients carried HCV genotype 4. The Sustained virological response was 100% and 92% in cirrhotics and noncirrhotics, respectively. There was no significant difference between groups in baseline IL-10 or IFN-gamma. In noncirrhotics, IL-10 showed a significant reduction at Week 4 after treatment start. In cirrhotics, IL-10 showed a significant reduction at Week 4 after treatment starts and a significant reduction at Week 12 after the end of the treatment. At Week 12 after the end of the treatment, serum IL-10 levels were significantly lower in cirrhotics. IFN-γ showed nonsignificant changes in noncirrhotics. A significant increase of IFN-γ occurred in cirrhotics from Week 4 after treatment starts to 12 weeks after the end of the treatment. IFN-γ was significantly higher in cirrhotics at Week 12 after the end of the treatment. IFN-γ and IL-10 showed different correlations with laboratory markers.
Viral eradication induced by DAAs caused a significant change in IL-10 and IFN-gamma.
本研究分析了接受直接作用抗病毒药物(DAA)治疗的慢性丙型肝炎病毒(HCV)感染患者循环炎症细胞因子干扰素γ(IFN-γ)和白细胞介素(IL)-10(作为辅助性T细胞1型和辅助性T细胞2型免疫反应的主要细胞因子)水平的变化,并将它们与实验室指标相关联。
这项初步研究纳入了50例HCV单一感染患者,他们接受了12周或24周的DAA治疗。在治疗期间每月进行随访,并在治疗结束后3个月进行随访。除了FIB-4指数外,还通过瞬时弹性成像来确定肝脏疾病。使用酶联免疫吸附测定法对IFN-γ和IL-10进行分析。
所有患者均携带HCV基因4型。在肝硬化患者和非肝硬化患者中,持续病毒学应答率分别为100%和92%。两组患者在基线IL-10或IFN-γ水平上无显著差异。在非肝硬化患者中,治疗开始后第4周IL-10显著降低。在肝硬化患者中,治疗开始后第4周IL-10显著降低,治疗结束后第12周也显著降低。治疗结束后第12周,肝硬化患者的血清IL-10水平显著较低。在非肝硬化患者中,IFN-γ无显著变化。在肝硬化患者中,从治疗开始后第4周直至治疗结束后12周,IFN-γ显著升高。治疗结束后第12周,肝硬化患者的IFN-γ显著更高。IFN-γ和IL-10与实验室指标显示出不同的相关性。
DAA诱导的病毒清除导致IL-10和IFN-γ发生显著变化。