Chronic lymphocytic leukaemia: a disease of activated monoclonal B cells

被引:48
作者
Damle, Rajendra N. [1 ,2 ]
Calissano, Carlo [1 ]
Chiorazzi, Nicholas [1 ,3 ,4 ]
机构
[1] Feinstein Inst Med Res, Manhasset, NY 11030 USA
[2] NYU Sch Med, Dept Med, New York, NY USA
[3] Albert Einstein Coll Med, Dept Cell Biol, Bronx, NY 10467 USA
[4] Albert Einstein Coll Med, Dept Med, Bronx, NY 10467 USA
关键词
B lymphocyte; chronic lymphocytic leukaemia; cell proliferation; kinetics; antigen receptor; antigen; CHRONIC LYMPHOPROLIFERATIVE DISORDERS; SURFACE-ANTIGEN EXPRESSION; GENE MUTATION STATUS; CD38; EXPRESSION; T-CELL; TELOMERASE ACTIVITY; SIGNALING PATHWAYS; ZAP-70; CLONAL EXPANSION; DNA METHYLATION;
D O I
10.1016/j.beha.2010.02.001
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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 Cl 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. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:33 / 45
页数:13
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