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.

Gobbi, G., Mirandola, P., Malinverno, C., Sponzilli, I., Carubbi, C., Ricci, F., et al. (2008). Aberrant expression of B203.13 antigen in acute lymphoid leukemia of B-cell origin. INTERNATIONAL JOURNAL OF ONCOLOGY, 33, 2-371 [10.3892/ijo_00000017].

Aberrant expression of B203.13 antigen in acute lymphoid leukemia of B-cell origin.

PASQUANTONIO, GUIDO;
2008-08-02

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 leukemia.
2-ago-2008
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore MED/28 - MALATTIE ODONTOSTOMATOLOGICHE
English
Con Impact Factor ISI
Gobbi, G., Mirandola, P., Malinverno, C., Sponzilli, I., Carubbi, C., Ricci, F., et al. (2008). Aberrant expression of B203.13 antigen in acute lymphoid leukemia of B-cell origin. INTERNATIONAL JOURNAL OF ONCOLOGY, 33, 2-371 [10.3892/ijo_00000017].
Gobbi, G; Mirandola, P; Malinverno, C; Sponzilli, I; Carubbi, C; Ricci, F; Binazzi, R; Basso, G; Giuliani Piccari, G; Ramazzotti, G; Pasquantonio, G; Cocco, L; Vitale, M
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/61527
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