Carrasco Javier, Godelaine Danièle, Van Pel Aline, Boon Thierry, van der Bruggen Pierre
Ludwig Institute for Cancer Research, 74 avenue Hippocrate, UCL 7459, B-1200 Brussels, Belgium.
Blood. 2006 Nov 1;108(9):2897-905. doi: 10.1182/blood-2005-11-007237. Epub 2006 Jul 20.
The expression of CD45RA on CCR7- human CD8+ memory T cells is widely considered to be a marker of terminal differentiation. We studied the time course of CD45RA and CCR7 expression on human antitumoral cytotoxic T lymphocyte (CTL) clones and blood CD8+ T cells after antigenic stimulation. Our results indicate that CD45RA+ CCR7- CD8+ T cells are resting memory cells that, upon antigenic stimulation and during the next 10 days, proliferate, lose CD45RA, and transiently acquire CCR7. In the absence of further antigenic stimulation, they progressively re-express CD45RA and become CD45RA+ CCR7-. We conclude that the expression of CD45RA on these cells is indicative of the time elapsed since the last antigenic stimulation rather than the incapacity to proliferate or particularly high lytic potential. This concept leads to a reinterpretation of the significance of the presence of CD45RA+ CD8+ memory cells in patients affected by viral infections or by cancer.
CCR7阴性的人类CD8⁺记忆T细胞上CD45RA的表达被广泛认为是终末分化的标志物。我们研究了抗原刺激后人类抗肿瘤细胞毒性T淋巴细胞(CTL)克隆和血液CD8⁺T细胞上CD45RA和CCR7表达的时间进程。我们的结果表明,CD45RA⁺CCR7⁻CD8⁺T细胞是静息记忆细胞,在抗原刺激后及随后的10天内,它们会增殖,丢失CD45RA,并短暂获得CCR7。在没有进一步抗原刺激的情况下,它们会逐渐重新表达CD45RA并变为CD45RA⁺CCR7⁻。我们得出结论,这些细胞上CD45RA的表达指示的是自上次抗原刺激以来所经过的时间,而非增殖能力的丧失或特别高的裂解潜力。这一概念导致对病毒感染或癌症患者中CD45RA⁺CD8⁺记忆细胞存在意义的重新解释。