Fig. 1.
Fig. 1. A reduced lymphoproliferative response of PBMCs in the post–T-cell depletion period results from a reduced proliferative capacity of T cells. / To exclude that after T-cell–depleting therapy depressed lymphoproliferative responses of PBMCs simply reflect a reduced number of proliferating T cells, the proliferative responses to stimulation with immobilized anti-CD3 of 1 × 105 PBMCs were compared with that of an enriched T-cell population (7.5 × 104) recombined with enriched monocytes (2.5 × 104). Blank bars, control cells; black bars, patient cells. The bars represent the cpm (mean ± SEM) of triplicate cultures. Patient cells were obtained from an 8-year-old boy with ALL (patient 17) 3 months after matched unrelated donor (MUD)–BMT.

A reduced lymphoproliferative response of PBMCs in the post–T-cell depletion period results from a reduced proliferative capacity of T cells.

To exclude that after T-cell–depleting therapy depressed lymphoproliferative responses of PBMCs simply reflect a reduced number of proliferating T cells, the proliferative responses to stimulation with immobilized anti-CD3 of 1 × 105 PBMCs were compared with that of an enriched T-cell population (7.5 × 104) recombined with enriched monocytes (2.5 × 104). Blank bars, control cells; black bars, patient cells. The bars represent the cpm (mean ± SEM) of triplicate cultures. Patient cells were obtained from an 8-year-old boy with ALL (patient 17) 3 months after matched unrelated donor (MUD)–BMT.

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