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CD 13 expression in B cell malignancies is a hallmark of plasmacytic differentiation
Author(s) -
Raimbault Anna,
MachherndlSpandl Sigrid,
Itzykson Raphaël,
Clauser Sylvain,
Chapuis Nicolas,
Mathis Stéphanie,
Lauf Jeroen,
Alary AnneSophie,
Burroni Barbara,
Kosmider Olivier,
Fontenay Michaela,
Béné Marie C.,
Durrieu Françoise,
Bettelheim Peter,
Bardet Valérie
Publication year - 2019
Publication title -
british journal of haematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.907
H-Index - 186
eISSN - 1365-2141
pISSN - 0007-1048
DOI - 10.1111/bjh.15584
Subject(s) - lymphoplasmacytic lymphoma , waldenstrom macroglobulinemia , flow cytometry , b cell , lymphoma , immunophenotyping , pathology , biology , medicine , immunology , antibody
Summary The diagnosis of Waldenström Macroglobulinaemia ( WM )/lymphoplasmacytic lymphoma ( LPL ) remains one of exclusion because other B‐cell lymphoproliferative disorders (B‐ LPD ), such as marginal zone lymphoma ( MZL ), can fulfil similar criteria, including MYD 88 L265P mutation. It has been suggested that expression of the myeloid marker CD 13 (also termed ANPEP ) is more frequent in LPL than in other B‐ LPD and has also been described on normal and malignant plasma cells. Here, CD 13 expression was tested in a cohort of 1037 B‐ LPD patients from 3 centres by flow cytometry. The percentage of CD 13‐expressing cells was found to be variable among B‐ LPD but significantly higher in WM / LPL (median 31% vs. 0% in non‐ WM / LPL , P < 0·001). In multivariate linear regression, CD 13 expression remained significantly associated with a diagnosis of WM / LPL ( P < 0·001). A cut‐off value of 2% of CD 19 + cells co‐expressing CD 13 yielded the best diagnostic performance for WM / LPL assertion. This was further improved by association with the presence or absence of IgM paraprotein. Finally, given that previously published transcriptomic data revealed no difference in CD 13 (also termed ANPEP ) mRNA between normal and pathological B‐cells, the hypothesis of some post‐transcriptional regulation must be favoured. These results suggest that testing for CD 13 expression in routine flow cytometry panels could help to discriminate WM / LPL from other B‐ LPD .