Long-term cultures (LTC) and immunodeficient (NOD/SCID) mice have been
used to quantitate and characterize primitive malignant progenitors f
rom patients with acute myelogenous leukemia (AML). In 5-week-old LTC
of cells from newly diagnosed patients with AML cytogenetically abnorm
al as well as normal progenitors could be easily detected and their nu
mbers increased by cytokine supplements to the cultures. Sixty percent
of AML samples will engraft in NOD/SCID mouse marrow. The frequency a
nd level of engraftment of human cells detected appears to vary among
the different subtypes of AML but is not generally affected by treatme
nt of the mice with human cytokines. Both the LTC and NOD/SCID mouse a
ssay show promise as tools to allow characterization of differences be
tween leukemic stem cells which maintain malignant hematopoiesis in in
dividual patients and, more importantly, between these cells and their
normal stem cell counterparts.