Abstract
Very low levels of circulating monoclonal B-cell subpopulations can now be detected in apparently healthy individuals using flow cytometry. We propose the term 'monoclonal B-cell lymphocytosis' (MBL) to describe this finding. The aim of this document is to provide a working definition of MBL for future clinical, epidemiological and laboratory studies. We propose that the detection of a monoclonal B-cell population by light chain restriction is sufficient to define this condition in individuals not meeting the diagnostic criteria for other B-lymphoproliferative disorders. The majority of individuals with MBL will have cells that are indistinguishable from chronic lymphocytic leukaemia (CLL). However, this blood cell clonal expansion of CD5+ or CD5- B-lymphocytes is age-dependent and immunophenotypic heterogeneity is common. Longitudinal studies are required to determine whether MBL is a precursor state to CLL or other B-lymphoproliferative disease in a situation analogous to a monoclonal gammopathy of undetermined significance and myeloma. Future studies of MBL should be directed towards determining its relationship to clinical disease, particularly in individuals from families with a genetic predisposition to developing CLL.
Original language | English (US) |
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Pages (from-to) | 325-332 |
Number of pages | 8 |
Journal | British journal of haematology |
Volume | 130 |
Issue number | 3 |
DOIs | |
State | Published - Aug 2005 |
Keywords
- B cells
- Early detection
- Familial chronic lymphocytic leukaemia
- Monoclonal B-cell lymphocytosis
- Surrogate biomarker
ASJC Scopus subject areas
- Hematology