Tester Ian, Smyk-Pearson Susan, Wang Ping, Wertheimer Anne, Yao Ermei, Lewinsohn David M, Tavis John E, Rosen Hugo R
Department of Medicine, Portland Veterans Administration Medical Center, Oregon Health Science University, Portland, OR 97239, USA.
J Exp Med. 2005 Jun 6;201(11):1725-31. doi: 10.1084/jem.20042284.
Acute infection with hepatitis C virus (HCV) rarely is identified, and hence, the determinants of spontaneous resolution versus chronicity remain incompletely understood. In particular, because of the retrospective nature and unknown source of infection in most human studies, direct evidence for emergence of escape mutations in immunodominant major histocompatibility complex class I-restricted epitopes leading to immune evasion is extremely limited. In two patients infected accidentally with an identical HCV strain but who developed divergent outcomes, the total lack of HCV-specific CD4+ T cells in conjunction with vigorous CD8+ T cells that targeted a single epitope in one patient was associated with mutational escape and viral persistence. Statistical evidence for positive Darwinian selective pressure against an immunodominant epitope is presented. Wild-type cytotoxic T lymphocytes persisted even after the cognate antigen was no longer present.
丙型肝炎病毒(HCV)的急性感染很少被识别出来,因此,关于自发清除与慢性化的决定因素仍未完全了解。特别是,由于大多数人体研究的回顾性性质以及感染源不明,免疫显性主要组织相容性复合体I类限制性表位中导致免疫逃逸的逃逸突变出现的直接证据极为有限。在两名意外感染相同HCV毒株但结局不同的患者中,一名患者完全缺乏HCV特异性CD4 + T细胞,同时针对单个表位的强力CD8 + T细胞与突变逃逸和病毒持续存在有关。本文提供了针对免疫显性表位的正向达尔文选择压力的统计证据。即使同源抗原不再存在,野生型细胞毒性T淋巴细胞仍持续存在。