Niewiesk S, Daenke S, Parker C E, Taylor G, Weber J, Nightingale S, Bangham C R
Institute of Molecular Medicine, John Radcliffe Hospital, Headington, Oxford, United Kingdom.
J Virol. 1994 Oct;68(10):6778-81. doi: 10.1128/JVI.68.10.6778-6781.1994.
Human T-cell leukemia virus type I (HTLV-1) causes T-cell leukemia and tropical spastic paraparesis (TSP) in a minority of infected people, whereas the majority remain healthy. No association between a particular HTLV-I sequence and disease manifestation has been found in previous studies. We studied here the sequence variability of the gene for the HTLV-I Tax protein, which is the dominant target antigen of the very strong cytotoxic T-lymphocyte response to the virus. In HTLV-I infection, the intraisolate nucleotide variability is much greater than the variability between isolates. The predicted protein sequence of Tax was significantly more variable in the healthy seropositive individuals' provirus than in those of the patients with TSP. Thus, tax sequence heterogeneity, rather than the presence of particular sequences, distinguishes healthy HTLV-I-seropositive individuals from patients with TSP.
人类嗜T淋巴细胞病毒I型(HTLV-1)在少数感染者中会引发T细胞白血病和热带痉挛性截瘫(TSP),而大多数感染者仍保持健康。此前的研究未发现特定HTLV-I序列与疾病表现之间存在关联。我们在此研究了HTLV-I Tax蛋白基因的序列变异性,该蛋白是针对该病毒的极强细胞毒性T淋巴细胞反应的主要靶抗原。在HTLV-I感染中,分离株内部的核苷酸变异性远大于分离株之间的变异性。Tax的预测蛋白序列在健康血清阳性个体的前病毒中比在TSP患者的前病毒中变异程度显著更高。因此,是tax序列的异质性而非特定序列的存在,将健康的HTLV-I血清阳性个体与TSP患者区分开来。