CD13 expression in B cell malignancies is a hallmark of plasmacytic differentiation.


Journal

British journal of haematology
ISSN: 1365-2141
Titre abrégé: Br J Haematol
Pays: England
ID NLM: 0372544

Informations de publication

Date de publication:
02 2019
Historique:
received: 19 05 2018
accepted: 24 07 2018
pubmed: 11 9 2018
medline: 28 12 2019
entrez: 11 9 2018
Statut: ppublish

Résumé

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 MYD88 L265P mutation. It has been suggested that expression of the myeloid marker CD13 (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, CD13 expression was tested in a cohort of 1037 B-LPD patients from 3 centres by flow cytometry. The percentage of CD13-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, CD13 expression remained significantly associated with a diagnosis of WM/LPL (P < 0·001). A cut-off value of 2% of CD19

Identifiants

pubmed: 30198568
doi: 10.1111/bjh.15584
doi:

Substances chimiques

Neoplasm Proteins 0
RNA, Messenger 0
RNA, Neoplasm 0
CD13 Antigens EC 3.4.11.2

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

625-633

Informations de copyright

© 2018 British Society for Haematology and John Wiley & Sons Ltd.

Auteurs

Anna Raimbault (A)

Service d'Hématologie Biologique, Hôpitaux Universitaires Paris Centre, Université Paris Descartes, Paris, France.

Sigrid Machherndl-Spandl (S)

Department of Haematology, Internal Oncology and Stem Cell Transplantation, Ordensklinikum Linz Elisabethinen Hospital, Linz, Austria.

Raphaël Itzykson (R)

Service d'Hématologie Clinique, Hôpitaux Universitaires Saint Louis, Lariboisière, Fernand Widal, Université Paris Diderot, Paris, France.

Sylvain Clauser (S)

Service d'Hématologie-Immunologie-Transfusion, Hôpitaux Universitaires Paris Ile De France Ouest, Université Versailles Saint Quentin, Boulogne, France.

Nicolas Chapuis (N)

Service d'Hématologie Biologique, Hôpitaux Universitaires Paris Centre, Université Paris Descartes, Paris, France.

Stéphanie Mathis (S)

Service d'Hématologie Biologique, Hôpitaux Universitaires Paris Centre, Université Paris Descartes, Paris, France.
Service d'Hématologie Clinique, Hôpitaux Universitaires Saint Louis, Lariboisière, Fernand Widal, Université Paris Diderot, Paris, France.

Jeroen Lauf (J)

Department of Haematology, Internal Oncology and Stem Cell Transplantation, Ordensklinikum Linz Elisabethinen Hospital, Linz, Austria.

Anne-Sophie Alary (AS)

Service d'Hématologie Biologique, Hôpitaux Universitaires Paris Centre, Université Paris Descartes, Paris, France.

Barbara Burroni (B)

Service d'Anatomopathologie, Hôpitaux Universitaires Paris Centre, Université Paris Descartes, Paris, France.

Olivier Kosmider (O)

Service d'Hématologie Biologique, Hôpitaux Universitaires Paris Centre, Université Paris Descartes, Paris, France.

Michaela Fontenay (M)

Service d'Hématologie Biologique, Hôpitaux Universitaires Paris Centre, Université Paris Descartes, Paris, France.

Marie C Béné (MC)

Service d'Hématologie Biologique, CHU et Université de Nantes, Nantes, France.

Françoise Durrieu (F)

Hématologie Biologique, Institut Bergonié, Bordeaux, France.

Peter Bettelheim (P)

Department of Haematology, Internal Oncology and Stem Cell Transplantation, Ordensklinikum Linz Elisabethinen Hospital, Linz, Austria.

Valérie Bardet (V)

Service d'Hématologie-Immunologie-Transfusion, Hôpitaux Universitaires Paris Ile De France Ouest, Université Versailles Saint Quentin, Boulogne, France.

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Classifications MeSH