The B203.13 monoclonal antibody was developed by immunizing mice with the B/monocyte biphenotypic cell line B1b. During normal hematopoiesis B203.13 is expressed on a fraction of CD34+ cells, while on mature cells it is only present on B-lymphocytes. We tested this antibody as a marker of childhood B-acute lymphoblastic leukemia (B-ALL). Bone marrow aspirates from 139 cases of early B-ALL and 25 controls were studied. About 40% of the B-ALL patients expressed B203.13. In these patients, B203.13 was constantly co-expressed with CD10, but never co-expressed with CD20, contrary to the controls. The CD10(+)/B203.13(+) phenotype was specific to B-ALL, since CD10(+)/CD20(+) cells from common acute lymphoblastic leukemia (c-ALL) did not express B203.13. We concluded that the use of B203.13 in association with CD10 and CD20 provides meaningful information for distinguishing normal residual B-cells from leukemic B-lymphoblasts and that recurrence of a CD10(+)/B203.13(+) phenotype after transplantation may be a very early relapse indicator of early B-acute lymphoblastic leukemia
Aberrant expression of B203.13 antigen in acute lymphoid leukemia of B-cell origin / Gobbi, Giuliana; Mirandola, Prisco; Malinverno, C.; Sponzilli, Ivonne; Carubbi, Cecilia; Ricci, F.; Binazzi, R.; Basso, G.; GIULIANI PICCARI, G.; Ramazzotti, G.; Pasquantonio, G.; Cocco, L.; Vitale, Marco. - In: INTERNATIONAL JOURNAL OF ONCOLOGY. - ISSN 1019-6439. - 33:(2008), pp. 371-374. [10.3892/ijo_00000017]
Aberrant expression of B203.13 antigen in acute lymphoid leukemia of B-cell origin.
GOBBI, Giuliana;MIRANDOLA, Prisco;SPONZILLI, Ivonne;CARUBBI, Cecilia;VITALE, Marco
2008-01-01
Abstract
The B203.13 monoclonal antibody was developed by immunizing mice with the B/monocyte biphenotypic cell line B1b. During normal hematopoiesis B203.13 is expressed on a fraction of CD34+ cells, while on mature cells it is only present on B-lymphocytes. We tested this antibody as a marker of childhood B-acute lymphoblastic leukemia (B-ALL). Bone marrow aspirates from 139 cases of early B-ALL and 25 controls were studied. About 40% of the B-ALL patients expressed B203.13. In these patients, B203.13 was constantly co-expressed with CD10, but never co-expressed with CD20, contrary to the controls. The CD10(+)/B203.13(+) phenotype was specific to B-ALL, since CD10(+)/CD20(+) cells from common acute lymphoblastic leukemia (c-ALL) did not express B203.13. We concluded that the use of B203.13 in association with CD10 and CD20 provides meaningful information for distinguishing normal residual B-cells from leukemic B-lymphoblasts and that recurrence of a CD10(+)/B203.13(+) phenotype after transplantation may be a very early relapse indicator of early B-acute lymphoblastic leukemiaFile | Dimensione | Formato | |
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