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Blood, 1 June 2001, Vol. 97, No. 11, pp. 3491-3497
IMMUNOBIOLOGY
Expression of interferon consensus sequence binding protein
induces potent immunity against BCR/ABL-induced
leukemia
Ming Deng and
George Q. Daley
From the Whitehead Institute, Cambridge, Massachusetts,
and Division of Hematology/Oncology, Massachusetts General Hospital,
Harvard Medical School, Boston, MA.
Mice deficient in the interferon consensus sequence binding protein
(ICSBP) develop a disease resembling chronic myeloid leukemia (CML),
which in humans is caused by the BCR/ABL oncoprotein. Interferon- (IFN- ) induces ICSBP expression and is an effective therapy for CML.
This study examined whether enforced expression of ICSBP might
antagonize BCR/ABL-induced leukemia; results demonstrated that
ICSBP-modified cells generated a protective CD8+ cytotoxic
T-cell response against BCR/ABL-transformed BaF3 cells in a murine
leukemia model. ICSBP expression represents a novel means of
stimulating a host immune response to BCR/ABL+ leukemia
cells and a potential strategy for immunotherapy of CML.

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