High frequencies of leukemia stem cells in poor-outcome childhood precursor-B acute lymphoblastic leukemias

Abstract

In order to develop a xenograft model to determine the efficacy of new therapies against primary human precursor-B acute lymphoblastic leukemia (ALL) stem cells (LSCs), we used the highly immunodeficient non-obese diabetic (NOD).Cg-Prkdc(scid)IL2rg(tmlWjl)/SzJ (NOD-severe combined immune deficient (scid) IL2rg(-/-)) mouse strain. Intravenous transplantation of 2 of 2 ALL cell lines and 9 of 14 primary ALL cases generated leukemia-like proliferations in recipient mice by 1-7 months after transplant. Leukemias were retransplantable, and the immunophenotypes, gene rearrangements and expression profiles were identical or similar to those of the original primary samples. NOD-scid mice transplanted with the same primary samples developed similar leukemias with only a slightly longer latency than did NOD-scid-IL2Rg(-/-) mice. In this highly sensitive NOD-scid-IL2Rg(-/-)-based assay, 1-100 unsorted primary human ALL cells from five of five tested patients, four of whom eventually experienced leukemia relapse, generated leukemias in recipient mice. This very high frequency of LSCs suggests that a hierarchical LSC model is not valuable for poor-outcome ALL.

Figure 1

Nine of fourteen primary childhood precursor-B ALL cases and two of two cell lines generated leukemia-like proliferations in NOD-scid IL2rg^−/− mice 1–7 months after intravenous transplantation of one million cells (a). Massive splenomegaly was the most prominent gross pathologic feature in all the mice (b, c), accompanied by replacement of blood, spleen and marrow by human cells with the blast morphology of the original precursor-B ALL cases and cell lines (d).