Typical Waldenstrom macroglobulinemia is derived from a B-cell arrested after cessation of somatic mutation but prior to isotype switch events

被引:66
作者
Sahota, SS [1 ]
Forconi, F
Ottensmeier, CH
Provan, D
Oscier, DG
Hamblin, TJ
Stevenson, FK
机构
[1] Southampton Univ Hosp, Tenovus Lab, Mol Immunol Grp, Southampton SO16 6YD, Hants, England
[2] St Bartholomews & Royal London Sch Med & Dent, Dept Hematol, London, England
[3] Royal Bournemouth Hosp, Dept Haematol, Bournemouth, Dorset, England
关键词
D O I
10.1182/blood.V100.4.1505.h81602001505_1505_1507
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
There exists a wide spectrum of IgM-secreting B-cell tumors with different clinical behavior. Knowledge of the V-H gene status can reveal their origin and clonal history. For Waldenstrom macroglobulinemia (WM), a distinct subtype of lymphoplasmacytic lymphoma, early data on limited sequences showed evidence for somatic mutation. A recent report of one case demonstrated Intraclonal mutational activity occurring after transformation, a characteristic of germinal center lymphomas. To extend the investigation, we have analyzed 7 cases of WM. VH genes were somatically mutated with no evidence of intraclonal variation in all cases. In contrast to IgM-secreting multiple myeloma, there was no evidence for isotype switch transcripts in any of the cases. These data support the concept that typical WM is derived from a B cell that has undergone somatic mutation prior to transformation, at a point where isotype switch events have not been initiated. (C) 2002 by The American Society of Hematology.
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页码:1505 / 1507
页数:3
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