Purcell R
Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892-0740, USA.
Hepatology. 1997 Sep;26(3 Suppl 1):11S-14S. doi: 10.1002/hep.510260702.
Our knowledge of hepatitis C virus (HCV) dates only from 1975, when non-A, non-B hepatitis was first recognized. It was not until 1989 that the genome of the virus was first cloned and sequenced, and expressed viral antigens used to develop serological assays for screening and diagnosis. HCV is in a separate genus of the virus family Flaviviridae. It is a spherical enveloped virus of approximately 50 nm in diameter. Its genome is a single-stranded linear RNA molecule of positive sense and consists of a 5' noncoding region, a single large open reading frame, and a 3' noncoding region. The open reading frame encodes at least three structural and six nonstructural proteins. The genome is characterized by significant genetic heterogeneity, based on which HCV isolates can be classified into six major genotypes and more than 50 subtypes. Even individual isolates of HCV are genetically heterogeneous (quasispecies diversity). Genetic heterogeneity of HCV is greatest in the amino-terminal end of the second envelope protein (hypervariable region 1). This region may represent a neutralization epitope that is under selective pressure from the host's humoral immune response. Infection with HCV proceeds to chronicity in more than 80% of cases, and even recovery does not protect against subsequent re-exposure to the virus. The development of a broadly protective vaccine against HCV will therefore require a better understanding of the molecular biology and immune response to this virus.
我们对丙型肝炎病毒(HCV)的了解始于1975年,当时首次确认了非甲非乙型肝炎。直到1989年,该病毒的基因组才首次被克隆、测序,并表达出用于开发筛查和诊断血清学检测的病毒抗原。HCV属于黄病毒科的一个独立属。它是一种直径约50纳米的球形包膜病毒。其基因组是一个正链单链线性RNA分子,由5'非编码区、一个单一的大开放阅读框和一个3'非编码区组成。该开放阅读框编码至少三种结构蛋白和六种非结构蛋白。该基因组的特点是具有显著的遗传异质性,基于此,HCV分离株可分为六个主要基因型和50多个亚型。甚至HCV的单个分离株在基因上也是异质的(准种多样性)。HCV的遗传异质性在第二个包膜蛋白的氨基末端(高变区1)最大。该区域可能代表一个中和表位,其受到宿主体液免疫反应的选择性压力。超过80%的HCV感染病例会发展为慢性,即使康复也不能防止随后再次接触该病毒。因此,开发一种针对HCV的广泛保护性疫苗将需要更好地了解该病毒的分子生物学和免疫反应。