Leukemic lymphoblasts in B-lineage acute lymphoblastic leukemia (ALL)
express morphologic, phenotypic and genotypic features which resemble
those of B lymphocyte progenitors in normal bone marrow. Normal immatu
re B cells and cells from most cases of B-lineage ALL rapidly die in v
itro unless they are supported by bone marrow-derived stromal feeder l
ayers. Techniques suitable for maintaining normal and leukemic immatur
e B cells in culture have been developed. Thus, the stromal cell types
and growth factors that generate a milieu suitable for immature B-cel
l development can now be elucidated. In addition, the similarities and
discrepancies in survival requirements of normal and leukemic B cell
precursors can be studied. We postulate that leukemic B cell precursor
s can survive and expand in microenvironments incapable of supporting
their normal counterparts, and that the study of the survival requirem
ents of ALL cells will provide indications about the aggressivity of t
he disease in vivo. In this review, we discuss the culture conditions
that support in vitro survival of human immature B cells, some of the
factors that influence their expansion, and the putative molecular bas
is for the prolonged life-span of leukemic lymphoblasts.