The Feinstein Institute for Medical Research, 350 Community Drive, Manhasset, NY 11030, USA.
Best Pract Res Clin Haematol. 2010 Mar;23(1):33-45. doi: 10.1016/j.beha.2010.02.001.
B cell-type chronic lymphocytic leukaemia (CLL) has long been considered a disease of resting lymphocytes. However, cell surface and intracellular phenotypes suggest that most CLL cells are activated cells, although only a small subset progresses beyond the G1 stage of the cell cycle. In addition, traditional teaching says that CLL cells divide rarely, and therefore the build-up of leukaemic cells is due to an inherent defect in cell death. However, in vivo labelling of CLL cells indicates a much more active rate of cell birth than originally estimated, suggesting that CLL is a dynamic disease. Here we review the observations that have led to these altered views of the activation state and proliferative capacities of CLL cells and also provide our interpretation of these observations in light of their potential impact on patients.
B 细胞型慢性淋巴细胞白血病(CLL)长期以来一直被认为是一种静止淋巴细胞疾病。然而,细胞表面和细胞内表型表明,大多数 CLL 细胞是激活细胞,尽管只有一小部分细胞能够超过细胞周期的 G1 期。此外,传统观点认为 CLL 细胞很少分裂,因此白血病细胞的积累是由于细胞死亡的固有缺陷。然而,CLL 细胞的体内标记表明,细胞生成的速度比最初估计的要快得多,这表明 CLL 是一种动态疾病。在这里,我们回顾了导致这些对 CLL 细胞激活状态和增殖能力的改变观点的观察结果,并根据它们对患者的潜在影响对这些观察结果进行了解释。