CCL3 chemokine expression by chronic lymphocytic leukemia cells orchestrates the composition of the microenvironment in lymph node infiltrates

被引:31
作者
Hartmann, Elena M. [1 ,2 ]
Rudelius, Martina [1 ,2 ]
Burger, Jan A. [3 ]
Rosenwald, Andreas [1 ,2 ]
机构
[1] Univ Wurzburg, Inst Pathol, Josef Schneider Str 2, D-97080 Wurzburg, Germany
[2] Ctr Comprehens Canc, Mainfranken, Germany
[3] Univ Texas Houston, MD Anderson Canc Ctr, Dept Leukemia, 1515 Holcombe Blvd, Houston, TX 77030 USA
关键词
lymph node microenvironment; T cells; CCL3; CD57; CLL; CD57(+) T-CELLS; B-CELLS; IFN-GAMMA; PROGRAMMED DEATH-1; PERIPHERAL-BLOOD; HELPER-CELLS; DISEASE; PD-1; PROLIFERATION; MARKER;
D O I
10.3109/10428194.2015.1068308
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Previous experiments demonstrated that survival and proliferation of chronic lymphocytic leukemia (CLL) cells depends upon complex cross-talk between CLL cells and accessory cells in the tissue microenvironment. To further dissect these interactions in situ, we analyzed lymph nodes from 43 different patients infiltrated by CLL cells for expression of the chemokine CCL3, Ki-67, macrophages, and T cell subsets by immunohistochemistry. CCL3 expression was detected in 24 of 43 cases (56%), particularly in prolymphocytes and paraimmunoblasts within the proliferation centers. Significantly higher numbers of CD3+ T cells and CD57+ cells were noticed in CCL3 positive cases. Furthermore, denser infiltration of CLL lymph node tissues by CD57+ cells correlated with higher proliferation rates of the CLL cells. In conclusion, we demonstrate an association of CCL3 expression by CLL cells with increased numbers of CD3+ T cells and CD57+ cells in the lymph node microenvironment, which may promote CLL cell survival and proliferation.
引用
收藏
页码:563 / 571
页数:9
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