Department of Infectious Diseases, Gastroenterology and Tropical Medicine, Ain Shams Faculty of Medicine, Cairo, Egypt.
Department of Molecular Biology and Biochemistry, Ain Shams Faculty of Medicine, Cairo, Egypt.
Am J Gastroenterol. 2014 Feb;109(2):199-211. doi: 10.1038/ajg.2013.427. Epub 2014 Jan 21.
The objective of this study was to characterize the factors that influence the outcome of exposure to hepatitis C virus (HCV) genotype 4 (HCV-G4) and the course of recent infection.
In this longitudinal study, we prospectively assessed the clinical, genetic, virological, and immunological parameters and retrospectively determined single-nucleotide polymorphisms at interleukin-28B (IL-28B) rs12979860 in a well-characterized large cohort recently exposed to HCV-G4.
A total of 136 subjects with acute HCV (new viremia, seroconversion, and HCV-specific T-cell responses) were identified. Forty-eight subjects (35%) had spontaneous viral clearance and 88 subjects developed chronic HCV of which 42 subjects were treated with pegylated interferon monotherapy, with a sustained virologic response (SVR) rate of 88%. Twenty-six subjects developed HCV-specific T-cell immune responses without detectable viremia or seroconversion. IL-28B-CC (odds ratio (OR) 14.22; P<0.0001), multispecific T-cell responses (OR=11.66; P<0.0001), >300 IU/l alanine aminotransferase (ALT) decline within 4 weeks (OR=6.83; P<0.0001), jaundice (OR=3.54; P=0.001), female gender (OR=2.39; P=0.007), and >2.5 log10 HCV-RNA drop within 8 weeks (OR=2.48; P=0.016) were independently associated with spontaneous clearance. ALT normalization and undetectable HCV-RNA predicted SVR. Exposed apparently uninfected participants had a higher frequency of IL-28B-CC than patients with unresolved acute HCV (P<0.001). IL-28B-CC was associated with multispecific T-cell response (r(2)=0.0.835; P<0.001).
IL-28B-CC genotype, multispecific HCV T-cell responses, rapid decline in ALT, and viral load predict spontaneous clearance and response to acute HCV-G 4 therapy. IL-28B-CC genotype correlates with developing early multispecific T-cell responses. These findings have important implications for predicting the outcome of HCV exposure and acute infection and identifying patients likely to benefit from therapy.
本研究旨在分析影响丙型肝炎病毒(HCV)基因型 4(HCV-G4)暴露后结局和近期感染进程的因素。
本纵向研究前瞻性评估了临床、遗传、病毒学和免疫学参数,并回顾性确定了新近感染 HCV-G4 的特征明确的大队列中白细胞介素 28B(IL-28B)rs12979860 单核苷酸多态性。
共发现 136 例急性 HCV(新病毒血症、血清转换和 HCV 特异性 T 细胞应答)患者。48 例(35%)自发清除病毒,88 例发展为慢性 HCV,其中 42 例接受聚乙二醇干扰素单药治疗,持续病毒学应答(SVR)率为 88%。26 例出现 HCV 特异性 T 细胞免疫应答,但无病毒血症或血清转换。IL-28B-CC(比值比(OR)14.22;P<0.0001)、多特异性 T 细胞应答(OR=11.66;P<0.0001)、4 周内 ALT 下降>300IU/l(OR=6.83;P<0.0001)、黄疸(OR=3.54;P=0.001)、女性(OR=2.39;P=0.007)和 8 周内 HCV-RNA 下降>2.5log10(OR=2.48;P=0.016)与自发清除相关。ALT 正常化和 HCV-RNA 不可检测预测 SVR。表现为未感染者的 IL-28B-CC 频率高于未解决的急性 HCV 患者(P<0.001)。IL-28B-CC 与多特异性 HCV T 细胞应答相关(r(2)=0.0.835;P<0.001)。
IL-28B-CC 基因型、多特异性 HCV T 细胞应答、ALT 快速下降和病毒载量可预测急性 HCV-G4 治疗的自发清除和应答。IL-28B-CC 基因型与早期多特异性 T 细胞应答相关。这些发现对预测 HCV 暴露和急性感染的结局以及确定可能从治疗中获益的患者具有重要意义。