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Immunology. 1994 Nov;83(3):397-403.
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本文引用的文献

1
Differential genome-wide array-based methylation profiles in prognostic subsets of chronic lymphocytic leukemia.慢性淋巴细胞白血病预后亚组中基于全基因组芯片的差异甲基化图谱。
Blood. 2010 Jan 14;115(2):296-305. doi: 10.1182/blood-2009-07-232868. Epub 2009 Nov 6.
2
In vivo intraclonal and interclonal kinetic heterogeneity in B-cell chronic lymphocytic leukemia.B 细胞慢性淋巴细胞白血病体内克隆内和克隆间动力学异质性。
Blood. 2009 Nov 26;114(23):4832-42. doi: 10.1182/blood-2009-05-219634. Epub 2009 Sep 29.
3
Enhanced formation and survival of CD4+ CD25hi Foxp3+ T-cells in chronic lymphocytic leukemia.慢性淋巴细胞白血病中CD4+ CD25hi Foxp3+ T细胞的形成和存活增强。
Leuk Lymphoma. 2009 May;50(5):788-801. doi: 10.1080/10428190902803677.
4
In vivo dynamics of stable chronic lymphocytic leukemia inversely correlate with somatic hypermutation levels and suggest no major leukemic turnover in bone marrow.稳定型慢性淋巴细胞白血病的体内动力学与体细胞超突变水平呈负相关,提示骨髓中无主要的白血病细胞更新。
Cancer Res. 2008 Dec 15;68(24):10137-44. doi: 10.1158/0008-5472.CAN-08-2325.
5
Reduction of B cell turnover in chronic lymphocytic leukaemia.慢性淋巴细胞白血病中B细胞周转率的降低
Br J Haematol. 2008 Oct;143(2):240-7. doi: 10.1111/j.1365-2141.2008.07348.x. Epub 2008 Aug 15.
6
Relative value of ZAP-70, CD38, and immunoglobulin mutation status in predicting aggressive disease in chronic lymphocytic leukemia.ZAP-70、CD38及免疫球蛋白突变状态在预测慢性淋巴细胞白血病侵袭性疾病中的相对价值
Blood. 2008 Sep 1;112(5):1923-30. doi: 10.1182/blood-2007-05-092882. Epub 2008 Jun 24.
7
Chronic lymphocytic leukemia T cells show impaired immunological synapse formation that can be reversed with an immunomodulating drug.慢性淋巴细胞白血病T细胞表现出免疫突触形成受损,而这可以通过一种免疫调节药物逆转。
J Clin Invest. 2008 Jul;118(7):2427-37. doi: 10.1172/JCI35017.
8
CD38 expression in chronic lymphocytic leukemia is regulated by the tumor microenvironment.慢性淋巴细胞白血病中CD38的表达受肿瘤微环境调控。
Blood. 2008 May 15;111(10):5173-81. doi: 10.1182/blood-2007-08-108605. Epub 2008 Mar 7.
9
Constitutive activation of distinct BCR-signaling pathways in a subset of CLL patients: a molecular signature of anergy.慢性淋巴细胞白血病(CLL)患者亚群中不同BCR信号通路的组成性激活:一种无反应性的分子特征。
Blood. 2008 Jul 1;112(1):188-95. doi: 10.1182/blood-2007-09-111344. Epub 2008 Feb 21.
10
Clonal heterogeneity in chronic lymphocytic leukemia cells: superior response to surface IgM cross-linking in CD38, ZAP-70-positive cells.慢性淋巴细胞白血病细胞中的克隆异质性:CD38、ZAP-70阳性细胞对表面IgM交联的反应更佳
Haematologica. 2008 Mar;93(3):413-22. doi: 10.3324/haematol.11646. Epub 2008 Feb 20.

慢性淋巴细胞白血病:一种激活的单克隆 B 细胞疾病。

Chronic lymphocytic leukaemia: a disease of activated monoclonal B cells.

机构信息

The Feinstein Institute for Medical Research, 350 Community Drive, Manhasset, NY 11030, USA.

出版信息

Best Pract Res Clin Haematol. 2010 Mar;23(1):33-45. doi: 10.1016/j.beha.2010.02.001.

DOI:10.1016/j.beha.2010.02.001
PMID:20620969
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2921990/
Abstract

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.

摘要

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。