Functional phenotype of transformed human alpha beta and gamma delta T cells determined by different subgroup C strains of herpesvirus Saimiri

被引:50
作者
Fickenscher, H [1 ]
Bokel, C [1 ]
Knappe, A [1 ]
Biesinger, B [1 ]
Meini, E [1 ]
Fleischer, B [1 ]
Fleckenstein, B [1 ]
Broker, BM [1 ]
机构
[1] BERNHARD NOCHT INST TROP MED,ABT MED MIKROBIOL & IMMUNOL,D-20359 HAMBURG,GERMANY
关键词
D O I
10.1128/JVI.71.3.2252-2263.1997
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Based on sequence divergence in the transformation-relevant region, herpesvirus saimiri strains are classified into three subgroups. Only members of subgroup C transform human T lymphocytes to continuous interleukin-2-dependent growth in culture, In this study, human cord blood T cells were immortalized bg using different subgroup C strains (C488, C484, and C139), The resulting T-cell lines represented different types of T-cell clones. They were either CD4(+) or CD8(+) and expressed either the alpha beta or the gamma delta type of T-cell receptors. If transformed by the same virus strain, alpha beta and gamma delta clones were similar with respect to viral persistence, virus gene expression, proliferation, and Th1-type cytokine production. However, major differences were observed in T cells immortalized by different subgroup C strains. Strain C139 persisted at low copy number, compared to the high copy number of prototype C488. The transformation-associated genes stpC and tip of strain C488 were strongly induced after T-cell stimulation. The homologous genes of strain C139 were only weakly expressed and not induced after activation. After CD2 ligation, the C488-transformed T cells produced interleukin-2, whereas the C139-transformed cells did not. Correspondingly, the C139-transformed T cells were less sensitive to cyclosporin A. Sequence comparison from different subgroup C strains revealed a variability of the stpC/tip promoter region and of the Lck-binding viral protein Tip. Thus, closely related subgroup C strains of herpesvirus saimiri cause major differences in the functional phenotype of growth-transformed human T cells.
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收藏
页码:2252 / 2263
页数:12
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