The malignant clone in Waldenstrom's macroglobulinemia

被引:16
作者
Kriangkum, K
Taylor, BJ
Mant, MJ
Treon, SP
Belch, AR
Pilarski, LM
机构
[1] Univ Alberta, Dept Oncol, Edmonton, AB T6G 1Z2, Canada
[2] Cross Canc Inst, Edmonton, AB T6G 1Z2, Canada
[3] Univ Alberta, Dept Med, Edmonton, AB T6G 1Z2, Canada
[4] Dana Farber Canc Inst, Boston, MA 02115 USA
关键词
ISOTYPE SWITCH EVENTS; H GENE ANALYSIS; MULTIPLE-MYELOMA; SOMATIC MUTATION; CELL; LEUKEMIA; IGM; DIFFERENTIATION; EXPRESSION; EVOLUTION;
D O I
10.1053/sonc.2003.50061
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The unique IgM VDJ sequence that characterizes the malignant clone in Waldenstrom's macroglobulinemia (WM), termed clonotypic, was identified for 12 WM patients. The majority of WM patients (92%) had a clonotypic IgM from the VH3 family, with predominantly long CDR3 regions, characteristic of those found in antigen-stimulated populations. Clonotypic IgM transcripts were detected in both blood and bone marrow (BM), clearly identifying a blood-borne compartment of WM. Abnormal numbers of CD20+ B cells were usually detectable and expressed surface IgM. In most cases these cells also expressed surface IgD. Most WM patients lacked detectable CD 138+ plasma cells in either blood or BM. Longitudinal analysis suggests that phenotypic identification of B cells in blood of WM patients is insufficient for monitoring disease. Although serum IgM had decreased and clonotypic transcripts were very weak for one patient, the number of CD20+ B cells increased dramatically. The lack of clonotypic transcripts suggests that the majority of these circulating B cells were polyclonal and were not part of the WM clone, indicating that monitoring of clonotypic IgM provides the most accurate identifier of WM cells. © 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:132 / 135
页数:4
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