Division of Infectious Diseases, Department of Medicine, Johns Hopkins School of Medicine, Baltimore, MD, USA.
Hepatology. 2012 Jun;55(6):1684-91. doi: 10.1002/hep.25575. Epub 2012 Apr 18.
The aim of this study is to determine whether early viral dynamics and evolution predict outcome of primary acute hepatitis C virus (HCV) infection. HCV- and human immunodeficiency virus-negative injection drug users were enrolled prospectively and followed monthly to identify acute HCV infection using RNA detection. Subjects with more than 1 month between HCV-RNA-negative and -positive visits were excluded to ensure stringent acute infection. Differences in medians of log-transformed viral RNA levels and evolutionary rates in each gene of a 5'-hemigenomic amplicon were assessed using Mann-Whitney's rank-sum test. Correlation coefficient was calculated using Spearman's rank order. Initial viremia level was 50-fold higher in subjects with spontaneous clearance (compared with persistence) of primary acute HCV infection (median, 7.1 versus 5.4 log(10) IU/mL; P = 0.002). Initial viremia level in subjects with interleukin (IL)28B-C allele at rs12979860 and clearance was higher than that in subjects with IL28B-T allele and persistence (P = 0.001). Evolutionary rates in the hypervariable region 1 (HVR1) region of the E2 gene were significantly higher in self-resolvers than those in persistence subjects during early infection, whereas other genes or regions had comparable rates. All major substitutions in HVR1 in persistence subjects were convergent changes, whereas over the same time interval clearance subjects displayed divergent evolution, indicating different immune responses between the two groups.
Spontaneous clearance of acute HCV infection is predicted by high initial viremia as well as favorable IL28B genotype and is associated with rapid envelope-sequence evolution. This linkage of host genetics, viral dynamics, and evolution provides new directions for mechanistic studies. (HEPATOLOGY 2012;55:1684-1691).
本研究旨在确定急性丙型肝炎病毒(HCV)感染的早期病毒动力学和进化是否可以预测结局。前瞻性招募 HCV 和人类免疫缺陷病毒(HIV)阴性的注射吸毒者,并每月随访以使用 RNA 检测确定急性 HCV 感染。为确保严格的急性感染,排除 HCV-RNA 阴性和阳性就诊时间间隔超过 1 个月的患者。使用曼-惠特尼秩和检验评估 5'-半基因组扩增子每个基因的对数转换病毒 RNA 水平和进化率的中位数差异。使用 Spearman 等级相关系数计算相关性。自发清除(与持续存在相比)急性 HCV 感染的患者初始病毒血症水平高 50 倍(中位数,7.1 对 5.4log(10)IU/mL;P = 0.002)。IL28B-C 等位基因 rs12979860 且清除的患者初始病毒血症水平高于 IL28B-T 等位基因且持续的患者(P = 0.001)。E2 基因高变区 1(HVR1)中早期感染时,自限性清除患者的进化率明显高于持续性患者,而其他基因或区域的进化率相当。持续性患者 HVR1 中的所有主要替换均为收敛性变化,而在同一时间间隔内清除患者显示出发散性进化,表明两组之间存在不同的免疫反应。
急性 HCV 感染的自发清除可预测为高初始病毒血症以及有利的 IL28B 基因型,并与包膜序列的快速进化相关。宿主遗传学、病毒动力学和进化之间的这种联系为机制研究提供了新的方向。(HEPATOLOGY 2012;55:1684-1691)。