Growth characteristics and expansion of human umbilical cord blood and estimation of its potential for transplantation in adults.

HE Broxmeyer, G Hangoc, S Cooper… - Proceedings of the …, 1992 - National Acad Sciences
HE Broxmeyer, G Hangoc, S Cooper, RC Ribeiro, V Graves, M Yoder, J Wagner
Proceedings of the National Academy of Sciences, 1992National Acad Sciences
We estimated whether single collections of cord blood contained sufficient cells for
hematopoietic engraftment of adults by evaluating numbers of cord blood and adult bone
marrow myeloid progenitor cells (MPCs) as detected in vitro with steel factor (SLF) and
hematopoietic colony-stimulating factors (CSFs). SLF plus granulocyte-macrophage (GM)-
CSF detected 8-to 11-fold more cord blood GM progenitors [colony-forming units (CFU)-GM]
than cells stimulated with GM-CSF or 5637 conditioned medium (CM), growth factors …
We estimated whether single collections of cord blood contained sufficient cells for hematopoietic engraftment of adults by evaluating numbers of cord blood and adult bone marrow myeloid progenitor cells (MPCs) as detected in vitro with steel factor (SLF) and hematopoietic colony-stimulating factors (CSFs). SLF plus granulocyte-macrophage (GM)-CSF detected 8- to 11-fold more cord blood GM progenitors [colony-forming units (CFU)-GM] than cells stimulated with GM-CSF or 5637 conditioned medium (CM), growth factors previously used to estimate cord blood CFU-GM numbers. SLF plus erythropoietin (Epo) plus interleukin 3 (IL-3) enhanced detection of cord blood multipotential (CFU-GEMM) progenitors 15-fold compared to stimulation with Epo plus IL-3. Under the same conditions, bone marrow CFU-GM and CFU-GEMM were only enhanced in detection 2- to 4- and 6- to 8-fold. Increased detection of cord blood CFU-GEMM correlated directly with decreased detection of cord blood erythroid burst-forming units (BFU-E). In contrast, adult bone marrow CFU-GEMM and BFU-E numbers were both enhanced by SLF plus Epo plus IL-3. This suggests that most cord blood BFU-E may actually be CFU-GEMM. Cord blood collections (n = 17) contained numbers of MPCs (especially CFU-GM) similar to the number found in nine autologous bone marrow collections. To assess additional sources of MPCs, the peripheral blood of 1-day-old infants was assessed. However, average concentrations of MPCs circulating in these infants were only 30-46% that in their cord blood. Expansion of cord blood MPCs was also evaluated. Incubation of cord blood cells for 7 days with SLF resulted in 7.9-, 2.2-, and 2.7-fold increases in numbers of CFU-GM, BFU-E, and CFU-GEMM compared to starting numbers; addition of a CSF with SLF resulted in even greater expansion of MPCs. The results suggest that cord blood contains a larger number of early profile MPCs than previously recognized and that there are probably sufficient numbers of cells in a single cord blood collection to engraft an adult. Although the expansion data must be considered with caution, as human marrow repopulating cells cannot be assessed directly, in vitro expansion of cord blood stem and progenitor cells may be feasible for clinical transplantation.
National Acad Sciences