Ibe M, Sakaguchi T, Tanaka K, Saito S, Yokota S, Tanaka T, Shimotohno K, Chujoh Y, Shiratori Y, Omata M, Miwa K, Takiguchi M
Department of Tumour Biology, Institute of Medical Science, University of Tokyo, Japan.
J Gen Virol. 1998 Jul;79 ( Pt 7):1735-44. doi: 10.1099/0022-1317-79-7-1735.
In order to clarify the role of cytotoxic T lymphocytes (CTL) in hepatitis C virus (HCV) infection, an HLA-B35-restricted cytotoxic T cell epitope of HCV was identified using a strategy called reverse immunogenetics. Twenty-eight of 53 HCV peptides carrying two anchor residues were selected as HLA-B3501 binding peptides. These peptides were used to induce the specific cytotoxic T cells in peripheral blood lymphocytes from a patient with acute hepatitis C. Six HLA-B3501 binding peptides induced the peptide-specific CTL. One (HPNIEEVAL) of five peptides was confirmed as the epitope by the specific T cell clones. A sequence identical to the epitope was detected in isolates of the virus from the patient and a strong CTL response to this epitope was observed in the acute phase of hepatitis C but not in the recovery phase. The specific CTL for this epitope were not detected in peripheral blood lymphocytes from patients with chronic hepatitis C. Together these results suggest that the CTL specific for this epitope have an important role in the elimination of the virus in the patient.
为阐明细胞毒性T淋巴细胞(CTL)在丙型肝炎病毒(HCV)感染中的作用,采用一种称为反向免疫遗传学的策略鉴定了HCV的一种HLA - B35限制性细胞毒性T细胞表位。携带两个锚定残基的53种HCV肽中的28种被选为HLA - B3501结合肽。这些肽用于诱导一名急性丙型肝炎患者外周血淋巴细胞中的特异性细胞毒性T细胞。六种HLA - B3501结合肽诱导出了肽特异性CTL。通过特异性T细胞克隆证实五种肽中的一种(HPNIEEVAL)为表位。在该患者的病毒分离株中检测到与该表位相同的序列,并且在丙型肝炎急性期观察到针对该表位的强烈CTL反应,但在恢复期未观察到。在慢性丙型肝炎患者的外周血淋巴细胞中未检测到针对该表位的特异性CTL。这些结果共同表明,针对该表位的CTL在患者体内病毒清除中具有重要作用。