Parker C E, Nightingale S, Taylor G P, Weber J, Bangham C R
Institute of Molecular Medicine, John Radcliffe Hospital, Headington, Oxford, United Kingdom.
J Virol. 1994 May;68(5):2860-8. doi: 10.1128/JVI.68.5.2860-2868.1994.
CD8+ T cells were freshly isolated from a human T-cell leukemia virus type I (HTLV-I)-infected patient with tropical spastic paraparesis. These cells, which were specific for HTLV-I Tax, simultaneously recognized a minimum of five, and possibly as many as seven, distinct peptide epitopes within the protein. A further Tax epitope was recognized after a short period of culture without exogenous peptide stimulation. All but one of these epitopes were clustered in the N-terminal third of Tax, and one of the epitopes was clearly immunodominant on two separate occasions of testing. Recognition of the immunodominant epitope was restricted by human leukocyte antigen (HLA) B15, and recognition of all the others was by HLA A2. Similar patterns of cytotoxic T lymphocyte recognition of the HLA A2-restricted Tax peptides in two healthy HTLV-I-seropositive individuals, each of whom carried the HLA A2 allele, were observed.
CD8 + T细胞是从一名患有热带痉挛性截瘫的人类I型嗜T细胞病毒(HTLV - I)感染患者体内新鲜分离出来的。这些针对HTLV - I Tax的细胞同时识别该蛋白内至少五个、可能多达七个不同的肽表位。在没有外源性肽刺激的短时间培养后,又识别出一个Tax表位。除了一个表位外,所有这些表位都聚集在Tax的N端三分之一区域,并且其中一个表位在两次独立测试中明显占主导地位。免疫显性表位的识别受人类白细胞抗原(HLA)B15限制,其他所有表位的识别受HLA A2限制。在两名健康的HTLV - I血清阳性个体中观察到了类似的细胞毒性T淋巴细胞对HLA A2限制的Tax肽的识别模式,这两名个体均携带HLA A2等位基因。