Abstract
B-cell precursor (BCP) leukemia is the most common form of childhood cancer and the second most common form of acute leukemia in adults. Human BCP leukemia was treated in a severe combined immunodeficient mouse model by targeting of the tyrosine kinase inhibitor Genistein (Gen) to the B cell-specific receptor CD19 with the monoclonal antibody B43. The B43-Gen immunoconjugate bound with high affinity to BCP leukemia cells, selectively inhibited CD19-associated tyrosine kinases, and triggered rapid apoptotic cell death. At less than one-tenth the maximum tolerated dose more than 99.999 percent of human BCP leukemia cells were killed, which led to 100 percent long-term event-free survival from an otherwise invariably fatal leukemia. The B43-Gen immunoconjugate might be useful in eliminating leukemia cells in patients who have failed conventional therapy.
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Dates
Type | When |
---|---|
Created | 18 years, 10 months ago (Oct. 27, 2006, 2:19 p.m.) |
Deposited | 1 year, 7 months ago (Jan. 14, 2024, 10:57 p.m.) |
Indexed | 2 months, 1 week ago (June 26, 2025, 2:42 p.m.) |
Issued | 30 years, 6 months ago (Feb. 10, 1995) |
Published | 30 years, 6 months ago (Feb. 10, 1995) |
Published Print | 30 years, 6 months ago (Feb. 10, 1995) |
@article{Uckun_1995, title={Biotherapy of B-cell precursor leukemia by targeting genistein to CD19-associated tyrosine kinases}, volume={267}, ISSN={1095-9203}, url={http://dx.doi.org/10.1126/science.7531365}, DOI={10.1126/science.7531365}, number={5199}, journal={Science}, publisher={American Association for the Advancement of Science (AAAS)}, author={Uckun, F. M. and Evans, W. E. and Forsyth, C. J. and Waddick, K. G. and Tuel-Ahlgren, L. and Chelstrom, L. M. and Burkhardt, A. and Bolen, J. and Myers, D. E.}, year={1995}, month=feb, pages={886–891} }