T. Alsaati et al., A NOVEL ANTIGEN DETECTED BY THE CBF.78 ANTIBODY FURTHER DISTINGUISHESANAPLASTIC LARGE-CELL LYMPHOMA FROM HODGKINS-DISEASE, Blood, 86(7), 1995, pp. 2741-2746
A novel antigen detected by the CBF.78 monoclonal antibody (MoAb) is s
trongly expressed on cortical thymocytes and weakly expressed on resti
ng peripheral T lymphocytes. Expression of the antigen is increased on
phytohemagglutinin (PHA)- and anti-CD3-activated T lymphocytes and on
Epstein-Barr virus-transformed B lymphocytes. The CBF.78 immunoprecip
itated a protein of 116 kD from resting and PHA-activated peripheral b
lood mononuclear cells. CBF.78 MoAb did not inhibit T-cell proliferati
on induced by anti-CD3 antibody. This MoAb was effective for immunosta
ining on paraffin sections after microwave-oven heating of tissue sect
ions. Among malignant lymphomas, the antigen recognized by CBF.78 MoAb
was found to be mainly expressed by T-cell lymphomas (49+ of 74), par
ticularly those of high-grade malignancy (31+ of 36), whereas only occ
asional B-cell lymphomas (4+ of 107) expressed the antigen. A distinct
ive pattern of reactivity was shown by 108 cases of anaplastic large c
ell lymphomas. Strong positivity for CBF.78 antibody was observed in 8
6+ of 108 cases, irrespective of B, T, or null phenotype. This multice
nter study suggests that CBF.78 MoAb could be of diagnostic value in d
ifferentiating Hodgkin's-like anaplastic large cell lymphomas from cas
es of Hodgkin's disease rich in neoplastic cells. Only a few cases of
Hodgkin's disease (13+ of 126) showed rare Reed-Sternberg cells that s
tained. In these few cases, staining was weak to moderate and confined
to cytoplasm. CBF.78 MoAb was nonreactive with all nonhematopoietic n
eoplasms examined (0+ of 48). Further studies should delineate the fun
ction of this new antigen and its clinical utility. (C) 1995 by The Am
erican Society of Hematology.