Division of Histocompatibility and Immunogenetics, Department of Pathology, University of Utah School of Medicine, Salt Lake City, Utah, USA.
Hum Immunol. 2011 May;72(5):379-85. doi: 10.1016/j.humimm.2011.02.010. Epub 2011 Mar 4.
Hepatitis C virus (HCV) has a high rate of replication and lacks RNA-proofreading capabilities, thereby leading to variant or mutant viruses circulating within the host as a quasispecies. Previous work in our laboratory identified viral variants that emerged in a class-II immunodominant epitope NS3(358-375) of the non-structural-3 (NS3) protein region of HCV, the sequence of which is based on genotype 1A, the most prevalent genotype in the United States. Further work suggested that positive immune selection pressure was driving viral variation. Paradoxically, viral variants account for only a small percentage of the circulating virus in human beings and in chimpanzees, suggesting that passive evasion is not the only means of escape by HCV. This observation suggests a unique pathogenesis for HCV as it persists in the host. In the current study, we hypothesize that viral variants are acting as altered peptide ligands (APLs). To test this hypothesis, we used cloned T cells specific for NS3(358-375) peptide, which demonstrated attenuated T-cell and interferon-γ (IFN-γ) responses to individual variant peptides, when compared with the NS3(358-375) stimulated T-cell clones. Furthermore, such variants could act as APLs, based on their ability to antagonize the IFN-γ proliferative responses of clones specific for NS3(358-375). In addition, major histocompatibility complex (MHC) class II tetramer staining demonstrated that variant peptide-MHC complexes were able to specifically bind to NS3(358-375) T-cell clones and that both the variant and NS3(358-375) tetramers were able to bind to the same CD4(+) T cells. Taken together, the results suggest that viral variants may act as APL to effectively blunt the T-cell response to an important HCV epitope.
丙型肝炎病毒(HCV)具有高复制率且缺乏 RNA 校对功能,因此导致宿主中存在准种形式的变异或突变病毒。我们实验室之前的工作鉴定出 HCV 非结构-3(NS3)蛋白区域的 II 类免疫显性表位 NS3(358-375)中出现的病毒变异,其序列基于美国最常见的基因型 1A。进一步的工作表明,正向免疫选择压力正在驱动病毒变异。矛盾的是,病毒变异仅占人类和黑猩猩循环病毒的一小部分,这表明被动逃避并非 HCV 逃避的唯一手段。这一观察结果表明 HCV 具有独特的发病机制,因为它在宿主体内持续存在。在当前的研究中,我们假设病毒变异作为改变的肽配体(APL)起作用。为了验证这一假设,我们使用针对 NS3(358-375)肽的克隆 T 细胞,与 NS3(358-375)刺激的 T 细胞克隆相比,这些克隆对单个变异肽的 T 细胞和干扰素-γ(IFN-γ)反应均减弱。此外,此类变体可以作为 APL,因为它们能够拮抗针对 NS3(358-375)的 T 细胞克隆的 IFN-γ增殖反应。此外,主要组织相容性复合体(MHC)II 类四聚体染色表明,变异肽-MHC 复合物能够特异性结合 NS3(358-375)T 细胞克隆,并且变异和 NS3(358-375)四聚体均能够结合相同的 CD4(+)T 细胞。综上所述,结果表明病毒变异可能作为 APL 有效地削弱对 HCV 重要表位的 T 细胞反应。