Summary:We report the effects exerted by cytokine combinations, including stem cell factor (SCF), interleukin-7, interleukin-4 and interleukin-2, on the amplification of T cells from cord blood (CB) mononuclear cells cultured for 10-11 days under serum-deprived conditions. Of all the combinations investigated, SCF+interleukin-7 sustained the best fold increase (FI) of total nucleated cells (FI ¼ 6.471.17), amplifying preferentially CD4 + over CD8 + T-cell subsets (FI ¼ 4.7270.79 vs 2.7371.2, respectively, Po0.05). The addition of interleukin-2 to this combination did not significantly increase the total number of cells generated (FI ¼ 7.472.27), but allowed preferential amplification of CD8 + over CD4 + T cells (FI ¼ 6.0470.14 vs 1.6770.6, respectively, Po0.05). Single-strand conformation polymorphism analysis of the T-cell receptor V b -chain rearrangements expressed by the expanded T cells indicated that the complexity of the T-cell repertoire had increased after 10 days of culture in the presence of SCF and IL-7. Interestingly, a modest expansion (FI ¼ 8.6771.5) of myeloid progenitor cells was also observed in these cultures. These results indicate that it is possible to expand specific T-cell subsets for adoptive immunotherapy without losing myeloid progenitor cells necessary for neutrophil recovery after CB transplantation, by modulating the cytokines added to the cultures.