Peter Medawar Building for Pathogen Research, University of Oxford, Oxford, UK.
Eur J Immunol. 2015 Jan;45(1):113-8. doi: 10.1002/eji.201445016. Epub 2014 Nov 17.
Murine CMV (MCMV) infection induces effector CD8(+) T cells that continue to increase in frequency after acute infection ("inflation") and are stably maintained at a high frequency, with up to 20% of the CD8(+) T-cell compartment being specific for one epitope, although the flexibility and turnover of these populations is not fully defined. Here we report that effector/memory CD8(+) T cells induced by MCMV can be paradoxically boosted following transient depletion of epitope specific CD8(+) T cells. Treatment of MCMV-infected mice with MHC-Class I-saporin tetramers led to partial (80-90%) depletion of epitope-specific CD8(+) T cells-rapidly followed by a rebound, leading to expansion and maintenance of up to 40% of total CD8(+) T cells, with minimal changes in response to a control epitope (M45). These data indicate the tight balance between host and virus during persistent infection and the functional flexibility of the "inflated" CD8(+) T cell responses during persistent infection.
鼠巨细胞病毒(MCMV)感染诱导效应 CD8(+)T 细胞,在急性感染后(“膨胀”)频率继续增加,并稳定维持在高频率,高达 20%的 CD8(+)T 细胞区室特异性针对一个表位,尽管这些群体的灵活性和周转率尚未完全确定。在这里,我们报告说,由 MCMV 诱导的效应/记忆 CD8(+)T 细胞可以在短暂耗尽表位特异性 CD8(+)T 细胞后被悖论性地增强。用 MHC 类 I-丝裂霉素 C 四聚体处理 MCMV 感染的小鼠导致表位特异性 CD8(+)T 细胞的部分(80-90%)耗竭-迅速反弹,导致高达 40%的总 CD8(+)T 细胞的扩增和维持,对对照表位(M45)的反应变化最小。这些数据表明在持续感染期间宿主和病毒之间存在着紧密的平衡,以及在持续感染期间“膨胀”的 CD8(+)T 细胞反应的功能灵活性。