1. CD1d expression on B-precursor acute lymphoblastic leukemia subsets with poor prognosis.
- Author
-
Fais, F., Tenca, C., Cimino, G., Coletti, V., Zanardi, S., Bagnara, D., Saverino, D., Zarcone, D., De Rossi, G., Ciccone, E., and Grossi, C. E.
- Subjects
- *
LEUKEMIA in children , *LYMPHOBLASTIC leukemia , *B cells , *TARGETED drug delivery , *IMMUNOTHERAPY , *T cells , *CELL-mediated cytotoxicity - Abstract
Acute lymphoblastic leukemia (ALL) is the most frequent malignancy of childhood. Although therapeutical advances have been achieved, some ALL subgroups still fare poorly. CD1d is a monomorphic molecule that provides a suitable target for immunotherapy in view of the characterization of a glycolipid,a-galactosylceramide (a-GalCer), capable of being presented to CD1d-restricted T cells with cytotoxic potential. We investigated CD1d expression in 80 pediatric B-cell precursor (BCP) ALL cases defined according to immunophenotype, cytogenetic features and age at onset. CD1d was detected on ALL cells in 15%of the patients. CD1d+ ALLs were significantly associated with infant leukemia, pro-B phenotype and mixed-lineage leukemia (MLL)/AF4 gene rearrangement. Accordingly, overall survival of patients with CD1d+ ALL was significantly shorter. CD1d+ leukemic blasts were able to presenta-GalCer via CD1d to cytotoxic CD1d-restricted T cells, which induced apoptosis of ALL cells that was inhibited by mAb to CD1d. CD1d+ blasts loaded witha-GalCer elicited cytokine secretion by CD1d-restricted T cells. Analysis of bone marrow (BM) cells derived from normal donors revealed that CD19+/CD1d+ cells were mostly mature B lymphocytes. However, a minority of BCPs expressed CD1d. Thus, expression of CD1d in ALL cases heralds an adverse prognosis but may provide a therapeutic tool.Leukemia (2005) 19, 551-556. doi:10.1038/sj.leu.2403671 Published online 3 March 2005 [ABSTRACT FROM AUTHOR]
- Published
- 2005
- Full Text
- View/download PDF