Co-expression of CD79a (JCB117) and CD3 by lymphoblastic lymphoma

Emanuela Pilozzi, Karen Pulford, Margaret T. Jones, Hans-Konrad Müller-Hermelink(University of Würzburg), Brunangelo Falini(University of Perugia), Elisabeth Ralfkiær(University of Copenhagen), Stefano Pileri(University of Bologna), Francesco Pezzella, Christine De Wolf‐Peeters(Universitair Ziekenhuis Leuven), Daniel A. Arber, Harald Stein(Freie Universität Berlin), David Y. Mason, Kevin C. Gatter
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Abstract

Acute lymphoblastic leukaemia/lymphoma is a malignant disorder derived from the clonal proliferation of lymphoid precursor cells. Whether the tumour cells are of B- or T-cell type is an important criterion for prognosis which has not been available previously to pathologists, due to the lack of a reliable early B-cell marker functioning on routinely processed material. This has changed with the production of monoclonal antibodies against the B-cell signalling molecule CD79a. CD79a is expressed on normal and neoplastic B cells from the early stages of B-cell maturation and has been considered to be B-cell-specific. Currently available antibodies against CD79a, in particular JCB117, allow the identification of B cells, and hence B lymphoblastic disease, in paraffin-embedded material. In this study, the expression of CD79a (JCB117) and CD3 has been investigated in 149 cases of T and 68 cases of B lymphoblastic leukaemia/lymphoma. For the first time, co-expression of CD79a (JCB117) and CD3 is reported in 10 per cent of cases of T lymphoblastic leukaemia/lymphoma. This finding raises questions about the co-expression of T- and B-cell markers in the development of lymphocytes, benign as well as malignant, and alerts pathologists to a potential problem in diagnosis.


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