A NOVEL ANTIGEN DETECTED BY THE CBF.78 ANTIBODY FURTHER DISTINGUISHESANAPLASTIC LARGE-CELL LYMPHOMA FROM HODGKINS-DISEASE

Citation
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
Citations number
33
Categorie Soggetti
Hematology
Journal title
BloodACNP
ISSN journal
00064971
Volume
86
Issue
7
Year of publication
1995
Pages
2741 - 2746
Database
ISI
SICI code
0006-4971(1995)86:7<2741:ANADBT>2.0.ZU;2-6
Abstract
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.